Understanding the Lymph System
I thought it would be helpful for readers to understand the lymph system, the anatomy, what it does, and how it helps with immunity.
Listed below are information pages that should be quite helpful and each page has many additional links for more a more in depth study.
Role of lymphangiogenesis in cancer.
BIOLOGY OF NEOPLASIA
J Clin Oncol. 2007 Sep
Sundar SS, Ganesan TS.
Department of Gynaecological Oncology, Cheltenham General Hospital,
Gloucestershire Hospitals Foundation Trust, Gloucestershire, United
Kingdom. sudhasun…@minox.demon.co.uk
Regional lymph node metastasis is a common event in solid tumors and
is considered a marker for dissemination, increased stage, and worse
prognosis. Despite rapid advances in tumor biology, the molecular
processes that underpin lymphatic invasion and lymph node metastasis
remain poorly understood. However, exciting discoveries have been made in the field of lymphangiogenesis in recent years. The identification of vascular endothelial growth factor ligands and cognate receptors involved in lymphangiogenesis, an understanding of the embryology of the mammalian lymphatic system, the recent isolation of pure populations of lymphatic endothelial cells, the investigation of lymphatic metastases in animal models, and the identification of markers that discriminate lymphatics from blood vessels at immunohistochemistry are current advances in the field of
lymphangiogenesis, and as such are the main focus of this article.
This review also evaluates evidence for lymphangiogenesis (ie, new
lymphatic vessel formation in cancer) and critically reviews current
data on the prognostic significance of lymphatic vascular density in
tumors. A targeted approach to block pathways of lymphangiogenesis
seems to be an attractive anticancer treatment strategy. Conversely,
promotion of lymphangiogenesis may be a promising approach to the
management of treatment-induced lymphedema in cancer survivors.
Finally, the implications of these developments in cancer therapeutics
and directions for future research are discussed.
INTRODUCTION
The importance of lymphatic metastases is well recognized in cancer
staging and treatment, with lymph node status determining
multimodality treatment in patients with solid tumors such as breast
cancer, colorectal cancer, and head and neck cancer. However, the
process of lymphatic invasion and metastasis to regional lymph nodes,
and whether tumors promote lymphangiogenesis (ie, new lymphatic vessel growth) in a manner similar to angiogenesis, remain poorly understood. Recent advances in the biology and pathology of lymphangiogenesis have provided new insights into the field of lymphatic vascular biology.
ANATOMY AND PHYSIOLOGY OF THE LYMPHATIC SYSTEM
The lymphatic system functions as a conduit for protein-rich fluid
extravasated from the cardiovascular system, has a critical role in
maintaining tissue homeostasis and fat absorption from the gut, and
also plays an important role in immune surveillance.1 It consists of a
hierarchical network of vessels, starting from capillaries formed by
single thin-walled lymphatic endothelial cell (LEC) layers, through to
larger diameter vessels that eventually connect to the venous system.
Unlike blood vessels, lymphatic capillaries lack a continuous basement
membrane and pericytes, demonstrate large infrequent endothelial gaps, and are anchored to the extracellular matrix by elastic fibers (anchor filaments). These features prevent the vessels from collapsing during changes in interstitial pressure and facilitate the uptake of soluble tissue components, even in high-pressure environments.1 The collecting lymphatic vessels contain valves that prevent lymph backflow and have a coating of perivascular smooth muscle cells that allow propulsion of lymph through the vessels.2
EMBRYOLOGY OF THE LYMPHATIC SYSTEM
The earliest event in lymphatic development is the polarized
expression of the homeobox transcription factor Prox-1 in a
subpopulation of endothelial cells in the cardinal vein, which through
budding and sprouting, give rise to the lymphatic system.3 The
vascular phenotype is the default fate of budding embryonic venous
endothelial cells; on expression of Prox-1, cells adopt a lymphatic
vascular phenotype.4 Prox-1 overexpression in human vascular
endothelial cells suppresses blood vessel–specific genes and
upregulates lymphatic endothelial specific cell transcripts.5,6
Homozygous disruption of the Prox gene in mouse embryos is lethal at
embryonic day E14 to E15, with the embryos showing severe chylous
ascites and no lymphatic vasculature.3 Functional inactivation of a
single allele of the homeobox gene Prox1 leads to adult-onset obesity
due to abnormal lymph leakage from mispatterned and ruptured lymphatic vessels; Prox1 heterozygous mice are a model for adult-onset obesity.7.
Vascular endothelial growth factor C (VEGF-C) is an essential
chemotactic and survival factor during lymphangiogenesis and is
required for the sprouting of the first lymphatic vessels from
embryonic veins.8 Homozygous deletion of VEGF-C leads to the complete absence of lymphatic vasculature in mouse embryos; heterozygous VEGF-C mice display severe lymphatic hyperplasia.8 Deletion of VEGF-D does not affect development of lymphatic vasculature, although exogenous VEGF-D rescues the impaired vessel sprouting in VEGF-C–/– embryos.8,9
Vascular endothelial growth factor receptor 3 (VEGFR-3) signaling may
confer lymphatic endothelial-like phenotypes to endothelial cells10;
VEGFR-3 deletion leads to defects in blood vessel remodeling and
embryonic death at mid-gestation, indicating an early blood vascular
function.11 VEGFR-2 signaling is required for the endothelial
differentiation of mouse embryonic stem cells induced by VEGF-C.10
The forkhead transcription factor FOXC2 may control the maturation
stage of lymphatic vascular development and is important in the
genesis of lymphatic valves.12 There may be complex roles for ephrin
B2 and the Eph receptors; a valine deletion of PDZ binding site of
ephrin B2 causes mice to have normal blood vascular structure but
disturbed maturation of lymphatic vessels and valves.13 Deficiency of
podoplanin leads to abnormally dilated and nonfunctioning superficial
lymphatic vessels in the skin of newborn mice.14 Neuropilin 2, which
was originally shown to act as a semaphorin receptor in the nervous
system, binds to VEGF-C in addition to VEGFR-3.15 Neuropilin 2–
deficient mice showed severe hypoplasia of lymphatic capillaries from
E13 to birth, but had normal collecting vessels16; these defects were
transient and surviving mice regenerated capillaries similar to
heterozygous VEGF-C mice. Mice deficient in angiopoietin-2 (Ang 2)
also show defects in lymphatic vasculature, which could be rescued by Ang 1.17 Integrin IXβ1 binds directly to VEGF-C/D, suggesting
crosstalk between VEGFR-3 signaling and integrin-mediated adhesion and migration of lymphatic endothelial cells.18 The syk/slp-76 signaling
pathway may be involved, given that mice with mutations in the protein receptor tyrosine kinase Syk or its substrate (the adaptor protein SLP-76) exhibit edema and ascites as well as arteriovenous
malformations.19 The secondary lymphoid organs (lymph nodes and
Peyer’s patches of the small intestine) are superimposed on the
lymphatic vessels from the primitive lymph sacs formed by migrating
Prox-1–positive endothelial cells.20 Thus, although the development of
the lymphatic system is not understood completely, it is now agreed
that Prox-1 and VEGF-C are essential, with a varied contribution from
other proteins.
LYMPHANGIOGENIC FACTORS VEGF-C/D AND RECEPTOR VEGFR-3
VEGF-C and -D are ligands for the receptor tyrosine kinase VEGFR-3
(Fig 1 ). The VEGF-C/VEGF-D/VEGFR-3 axis constitutes the signal
transduction system for lymphatic endothelial cell growth, migration,
and survival.26-31 These growth factors are secreted as full-length
inactive forms consisting of NH2- and COOH-terminal propeptides and a central VEGF homology domain containing receptor binding sites.32
Proteolytic cleavage with plasmin removes the propeptides to generate mature forms, consisting of dimers of the VEGF homology domain, that bind receptors with much greater affinity than the full-length forms. 33 VEGFR-3 stimulation alone protects the lymphatic endothelial cells from serum deprivation-induced apoptosis, and induces their growth and migration. These signals are transduced via a protein kinase C–dependent activation of the p42/p44 mitogen-activated protein kinase signaling cascade and via a wortmannin-sensitive induction of Akt phosphorylation.31
The specific biologic effects of VEGF-C are critically dependent on
its proteolytic processing in vivo. Proteolytically processed VEGF-C/
VEGF-D also activates VEGFR-2 and can induce blood vessel growth.
27,28,34,35 Conversely VEGF-A, which is the primary angiogenic factor binding to VEGFR-2, can induce lymphatic hyperplasia but cannot substitute for VEGF-C in lymphatic development.8,36 Lymphatic endothelial cells express VEGFR-236-41 and VEGF-A is able to induce lymphangiogenesis potently at the cellular level on lymphatic
endothelial cells, in xenografts, and in skin during inflammation and
tissue repair.36,38,42
The VEGF-C/VEGFR-3 axis, through upregulation of contactin-1 and
activation of the src-p38 mitogen-activated protein kinase C/enhancer binding protein-dependent pathway may regulate the invasive capacity in different types of cancer cells and contribute to the promotion of cancer cell metastasis.43 Insulinlike growth factors 1 and 2 also induce lymphangiogenesis in vivo.44 Hepatocyte growth factor (HGF) is a lymphangiogenic factor that may contribute to lymphatic metastasis when overexpressed in tumors.45 The growth of HGF-induced lymphatic vessels can be partially blocked by a soluble VEGFR-3, suggesting that HGF may stimulate lymphatic vessel growth through an indirect mechanism. Other novel lymphangiogenic factors include Ang 1 and 2.17,46 Cyclooxygenase-2 may have a regulatory role in VEGF-C synthesis.47 Thus, the VEGF-C/VEGF-D/VEGFR-3 axis is the main signal transduction system in lymphatics; other novel lymphangiogenic factors may have direct or indirect influences on this system.
Experimental models have enhanced our understanding of lymphatic
vascular biology. These include the isolation of LECs and the
establishment of LEC lines31,40,42,48 using lymphatic markers such as
VEGFR-3, podoplanin, lymph vessel endothelial hyaluronic acid receptor 1 (LYVE-1). The Xenopus laevis tadpole has also been identified as an animal model that can be genetically manipulated to identify new lymphangiogenesis candidates (similar to zebrafish for angiogenesis research).49,50
LYMPHANGIOGENIC FACTORS PROMOTE TUMOR METASTASIS
Data supporting the premise that expression of lymphangiogenic factors promotes metastasis comes from in vitro and in vivo work.21 First, immunohistochemical studies show that overexpression of VEGF-C in breast, colorectal, gastric, thyroid, and prostate cancers is
associated with poor prognosis.51,52 Similarly, the expression level
of VEGF-D is an independent prognostic factor in ovarian cancer53 and stimulates lymphangiogenesis and lymphatic metastasis in human ductal pancreatic cancer54; expression of VEGFR-3 by lymphatic endothelial cells is associated with lymph node metastasis in prostate cancer.55 Expression levels of VEGF-C (and less often VEGF-D) also strongly correlate with lymph node metastasis in more than 30 studies.56,57 However, these observations in clinical tumor samples are largely correlative.
Experimental studies in animal models demonstrate that the VEGF-C/VEGF- D/VEGFR-3 signaling axis can promote tumor lymphangiogenesis and the metastatic spread of tumor cells.58 Two approaches have been used:
either to overexpress these factors in cell lines and study the
effects in vitro and in vivo, or to block the signaling with
inhibitors of the signaling cascade and observe the effects on
lymphatic and distant organ metastases.58 VEGF-C overexpression in
breast cancer cells in mouse experiments potently increased
intratumoral lymphangiogenesis, resulting in significantly enhanced
metastasis to regional lymph nodes and to lungs.59 Both VEGF-C and
VEGF-D enhance tumor lymphangiogenesis and lymphatic metastasis in
xenotransplant and transgenic models, and this promotes sentinel node metastasis.30,59-61 Moreover, in a chemically induced skin
carcinogenesis model, VEGF-C–overexpressing tumors induced the
expansion of lymphatic vessels within sentinel lymph nodes before the
onset of metastasis and promoted cancer metastasis beyond the sentinel lymph nodes to distal lymph nodes and lungs.62 VEGF-C–overexpressing
human melanomas in nude mice also showed enhanced tumor angiogenesis, indicating a coordinated regulation of lymphangiogenesis and angiogenesis in melanoma progression.63 Furthermore, VEGF-C induced chemotaxis of macrophages in vitro and in vivo, revealing a potential function of VEGF-C as an immunomodulator.63,64 Tumor- associated macrophages express lymphatic endothelial growth factors and VEGFR-3, and are related to peritumoral lymphangiogenesis, which may play a role in tumor cell dissemination.65
Transgenic mice that overexpress VEGF-A strongly promote multistep
carcinogenesis on chemical stimuli and demonstrate active
proliferation of VEGFR-2–expressing tumor–associated lymphatic vessels as well as tumor metastasis to the sentinel and distant lymph nodes.37 VEGF-A–overexpressing primary tumors induced sentinel node lymphangiogenesis even before metastasizing and maintained their lymphangiogenic activity after metastasis to draining lymph nodes.37 Primary tumors may prepare their future metastatic site by producing lymphangiogenic factors that mediate their efficient transport to the sentinel lymph node.37,62 These effects of VEGF-A on lymphatic vessels may be secondary to the induction of lymphatic vascular permeability or to recruitment of the inflammatory cells that produce VEGF-C/VEGF-D. 66
Conversely, blocking VEGFR-3 signaling with gene transfection or
recombinant adenoviruses suppressed tumor lymphangiogenesis and lymph node metastasis67 in xenografts established with a highly metastatic lung cancer cell line. However, lung metastasis was not affected by the blockade. Expression of a soluble VEGFR-3 antibody in a highly metastatic mammary cancer cell line suppressed metastasis formation in regional lymph nodes and lungs of rats.68 Similar successful approaches using recombinant adenoviruses have been used in a melanoma model,69 VEGFR-3–blocking antibodies in gastric cancer,70 and RNA interference in mouse mammary models.71
The cellular mechanisms of lymphangiogenesis in human diseases are
currently unknown, and could involve division of local preexisting
endothelial cells or incorporation of circulating progenitors. In
renal transplants, potential lymphatic progenitor cells derive from
the circulation, transmigrate through the connective tissue stroma,
presumably as macrophages, and incorporate into the growing lymphatic vessel.72
LYMPHATIC VASCULAR MARKERS
The recent identification of novel lymphatic markers that can
accurately discriminate lymphatic vessels from blood vessels in tissue
sections (LYVE-1, podoplanin, β-chemokine receptor D6, macrophage
mannose receptor, desmoplakin, and D2-4073-76) has yielded new insight into mechanisms of metastasis. Of these, LYVE-1, D2-40, and podoplanin have been most commonly used in studies to assess the significance of lymphatic vessel density/lymphatic area as a prognostic variable in survival and as a tool for predicting lymph node status in cancer (Fig 2).
LYVE-1 is a lymph-specific receptor for hyaluronan (HA).74 LYVE-1
sequesters HA on lymph vessel endothelium, colocalizes with HA on the luminal surface of lymphatic vessels, and binds both soluble and
immobilized HA exclusively.77 However LYVE-1 is also expressed in
normal liver blood sinusoids in mice and humans,78 and has been
identified on macrophages.79 The mucin-type transmembrane glycoprotein podoplanin is a highly expressed lymphatic-specific gene in cultured human LECs,42,73 and D2-40 is a novel monoclonal antibody that reacts with an oncofetal antigen present in fetal germ cells75,80; both are highly reliable lymphatic endothelial markers. These antibodies seem equally efficient in identifying lymphatic vessels in formalin-fixed tissue sections.81,82
These markers have been used to assess the significance of lymphatic
vessel density, to determine its prognostic significance to predict
nodal metastases and survival, and to investigate lymphangiogenesis in primary human tumors, with conflicting results (Table 1). Certainly in head and neck cancer, convincing evidence exists to support new
lymphatic vessel proliferation,100 and high intratumoral lymphatic
vessels were clearly associated with a higher risk for local relapse
as well as with poor disease-specific prognosis.83 However, in breast
cancer84,101,102 intratumoral lymphatic vessels are absent and the
significance of peritumoral vessels is unclear. Contradictory results
exist in melanoma and cervical cancer, in which two large studies
suggest improved survival with high lymphatic counts and attribute
this effect to immune responses triggered by inflammatory stromal
reaction.81,85 However, two smaller studies in melanoma suggest that
increased lymphatic density was associated with sentinel node
metastasis and poor survival, and that lymphatic vessel density could
discriminate between melanomas that metastasized and those that did
not.86,87 To date, no published studies in human cancer have commented on the presence of intratumoral lymphatics within metastases.
There may be several explanations for these conflicting results.
First, the studies differed with respect to antibodies used and
methods of evaluation of lymphatic vessel density. Lymphatic vessel
density was assessed either in hot spots or in areas of the highest
concentration of lymphatic vessels, or across the whole tissue
section. The proceedings of the First International Consensus
Conference on the Methodology of Lymphangiogenesis Quantification have been published recently, and recommend double immunostaining with the D2-40 monoclonal antibody and proliferation marker anti–Ki-67 antibody to assess lymphangiogenesis and details methods of quantification of lymphatic vessel density.103 This should result in standardization of results in future studies.
In some solid tumors such as ovarian cancer, the tissue sections may
not represent the invasive front of the tumor.88 Lymphangiogenesis may be more relevant in some cancers (eg, head and neck cancers) and more subtle changes in lymphatic surface area may be contributory in other cancers (eg, melanoma).87 Finally, lymphatic metastases may be an early event, which loses its prognostic significance in advanced cancers; more focused studies of early stage cancers or preinvasive lesions to identify a potential lymphangiogenic switch may be relevant. Interestingly, lymphovascular invasion identified in tissue sections of tumors clearly has been documented to be a reliable prognostic variable predicting nodal metastasis and survival in breast and cervix cancer, and influences decision making for therapy in testicular cancer.104-106 Although some of the conflicting data on the prognostic significance of lymphatic vessel density in human cancers can be attributable to varying methods of immunohistochemistry, antibodies, and modes of counting58 used in these studies, lymphatic metastases in human cancers may be complex and may reflect changes in
surface area of lymphatics or tumor cell–LEC interaction rather than a
simple increase in number of draining capillaries.107
Finally, the debate continues about whether tumor lymphangiogenesis
exists in human cancer or whether tumor cells invade preexisting
lymphatics at the periphery of the tumors,108 given that increased
interstitial fluid pressures may result in collapsed intratumoral
lymphatics. Additional studies in other tumor types and investigation
of lymphatic vessel density and proliferation markers may clarify the
role of new lymph vessel formation and the significance of lymphatic
vessel density in cancer progression.
MECHANISMS OF TUMOR CELL ENTRY INTO LYMPHATICS IN CANCER
He et al109 investigated how tumor cells gain access into lymphatic
vessels and at what stage tumor cells initiate metastasis. VEGF-C
produced by tumor cells induced extensive lymphatic sprouting toward
the tumor cells, dilation of the draining lymphatic vessels, and a
significant increase in lymphatic vessel growth between 2 and 3 weeks
after tumor xenotransplantation, with concurrent lymph node
metastasis. These processes were blocked dose dependently by
inhibition of VEGFR-3 signaling. However, lymph node metastasis was
not suppressed if soluble antibody to VEGFR-3 was started at a later
stage after the tumor cells had already spread out, suggesting that
tumor cell entry into lymphatic vessels is a key step during tumor
dissemination via the lymphatics. Whereas lymphangiogenesis and lymph node metastasis were inhibited significantly by antibody to VEGFR-3, some tumor cells were still detected in the lymph nodes in some of the treated mice. This indicates that complete blockade of lymphatic metastasis may require the targeting of both tumor lymphangiogenesis and tumor cell invasion.
However, Wong et al110 demonstrated that xenografts established in the prostate cancer model using stable short interfering RNA inhibiting
VEGF-C resulted in reduction of tumor lymphangiogenesis by 99%, but
this did not affect lymph node metastasis, indicating that tumor-
secreted VEGF-C is necessary for lymphangiogenesis, but
lymphangiogenesis was unnecessary for lymph node metastasis.
Tumor cells may also use physiologic chemokine receptor ligand
interactions for metastasis. Human breast cancer express chemokine
receptors CXCR4 and CCR7, and their respective ligands, CXCL12
(stromal-cell derived factor 1) and CCL21 (secondary lymphoid
chemokine) are highly expressed in the target organs of breast cancer
metastasis.111 Isolated LECs also express stromal-cell derived factor
1 and secondary lymphoid chemokine, suggesting they can attract tumor cells through secretion of chemokines.40 Similarly, lymphatic
endothelium secretes chemokine CCL21 (secondary lymphoid chemokine), which binds to CC chemokine receptor 7 leading to chemoattraction and migration of mature dendritic cells from skin to lymph nodes; CC chemokine receptor 7 is also expressed in some malignant melanoma cell lines.112
In summary, VEGF-C/VEGF-D, acting through their receptor VEGFR-3,
promote lymphatic metastasis. This could involve intratumoral or
peritumoral lymphangiogenesis, or more subtle alterations in tumor
cell–LEC interactions, and inhibition of this signaling causes
inhibition of lymph node metastasis (Fig 3).
TARGETING LYMPHANGIOGENESIS
Lymphedema
Lymphedema can be primary (caused by genetic conditions) or secondary to infection, malignancy, surgery, and/or radiotherapy. Filariasis in tropical countries and breast cancer treatment in the industrialized world are leading causes.113 Promising lymphedema treatment has been achieved in preclinical models using viral gene transfer vectors that induce lymphangiogenic factors.114 VEGFC gene transduction induces growth of functional lymphatic vessels,115 whereas the mature form of VEGF-D is a very powerful inducer of angiogenesis.35 VEGF-C gene therapy was effective in mouse models that demonstrate hereditary lymphedema.15 VEGF-C apparently can reverse the abnormalities in tissue architecture that accompany chronic lymphatic insufficiency.116 Ang1 gene transfer to mouse skin promotes lymphangiogenesis while inhibiting vascular permeability.46,117 Potential adverse effects from
prolymphangiogenic approaches include stimulation of lymphatic vessel
growth in cancer patients that may enhance metastatic spread118 and modulation of the immune system.
Targeting Tumor Lymphatics to Inhibit Metastases
Inhibition of VEGF-C/VEGF-D/VEGFR-3 axis in animal models can inhibit
tumor lymphangiogenesis and lymph node metastases.59 In addition,
blocking mouse VEGFR-3 with specific inhibitors has been shown to
block new lymphatic vessel growth exclusively, with no effect on
either blood angiogenesis or function of existing lymphatic vessels.
119 Akin to antiangiogenesis strategies, potential antilymphangiogenic
strategies could involve blocking antibodies or molecules that compete
for VEGF-C/VEGF-D/VEGFR-3 signaling, gene therapy to inhibit
lymphangiogenesis, small molecule tyrosine kinase inhibitors, and
inhibitors of other novel lymphangiogenic factors.58 Monoclonal
antibodies that inhibit lymphangiogenesis and angiogenesis exist,
120,121 although to our knowledge no studies exist yet in the clinical
setting. Blocking of lymphangiogenesis will need to be evaluated in
the adjuvant or neoadjuvant setting in combination with cytotoxics and surgery for primary therapy; cancers of interest on the basis of
proven lymphangiogenesis in animal models would appear to be breast
cancer, melanoma, colorectal cancer, and gastric cancer.58 The recent identification of novel lymphangiogenic factors, including hepatocyte growth factor122 and angiopoietin,17 indicate that efficient antilymphangiogenic strategies may need to target additional
lymphangiogenic molecules.123
Lymphatics in normal tissue play an important role in maintaining
tissue homeostasis and maintenance of interstitial fluid pressure.
Xenograft models of cancer demonstrate high intratumoral interstitial
fluid pressure, resulting in collapsed and nonfunctional intratumoral
lymphatics,108 whereas peritumoral lymphatics induced under the
influence of VEGF-C or VEGF-A seem to function poorly with incompetent valves.36,124 Increased interstitial fluid pressure forms a barrier to transcapillary transport and is an obstacle in tumor treatment; it results in inefficient uptake of therapeutic agents. Lowering the tumor interstitial fluid pressure might be a useful approach to improving anticancer drug efficacy.125 Indeed, normalization of tumor vasculature resulting in improved blood supply and drug transport to solid tumors has been proposed as the rationale behind combination treatment with antiangiogenesis agents and conventional cytotoxic therapy.126 It would be interesting to determine if a similar role can be envisaged for blocking lymphangiogenesis.
Several inhibitors of angiogenesis are being evaluated in trials127:
bevazucimab (recombinant human monoclonal antibody to VEGF) has been shown to improve survival in colorectal cancer. VEGF-A potentiates lymphangiogenesis and evaluation of inhibition of lymphangiogenesis in translational studies incorporated into trials with angiogenesis inhibitors may yield useful information. Combination treatment with the anti–VEGFR-2 and anti–VEGFR-3 antibodies seems to have cumulative effects on metastases compared with treatment with each antibody alone, suggesting that a combination therapy with antiangiogenic agents may be a promising approach for controlling metastases.128
ADDITIONAL DIRECTIONS OF RESEARCH AND UNANSWERED QUESTIONS
The growth of primary and metastatic tumors is unequivocally dependent on angiogenesis; similar proof does not currently exist for
lymphangiogenesis. Several unanswered questions exist in this field.
What are the mechanisms that control tumor cell interactions with
lymphatic endothelium? Is there a lymphangiogenic predisposition that
causes metastasis? Is there a correlation between histologic
differentiation/aggressive phenotypes on pathology and
lymphangiogenesis? Why do tumor cells promote lymphangiogenesis?129 Laboratory-based research with LECs, animal models, and translational studies should shed light on these questions.
In conclusion, the field of lymphangiogenesis has witnessed rapid
development after a long hiatus; the identification of lymphangiogenic
factors and their receptors, identification of lymphatic vascular
markers, and the implications of their activity in normal physiology
and pathology have improved our understanding of lymphatic vascular
biology. In the context of cancer, it is clear that tumor
lymphangiogenesis occurs in some tumors; blocking this process might
inhibit metastasis to lymph nodes, and lymphatic vascular markers may
be useful as a prognostic indicator of metastatic risk in cancer.
Additional research will clarify whether novel molecules targeting the
lymphangiogenic process are useful adjuvants to conventional
chemotherapy, and the extent to which existing antiangiogenic agents
may influence inhibition of lymphangiogenesis. Finally, a greater
understanding of these processes, particularly in the field of tumor
cell interactions with lymphatic endothelial cells, will pave the way
for harnessing this knowledge in cancer therapeutics.
ACKNOWLEDGMENTS
We thank Cancer Research UK and Oxfordshire Health Services Research;
Sanjeev Manek, John Radcliffe Hospital, United Kingdom, and Kathleen
Romain, MD, Cheltenham General Hospital, United Kingdom, for
assistance with immunohistochemistry and pathology images; and S.
Madhusudan, PhD, Churchill Hospital, United Kingdom for helpful
comments.
Primary cutaneous Richter syndrome: prognostic implications and review of the literature.
J Am Acad Dermatol. 2009 Jan
The term Richter syndrome (RS) describes the transformation of chronic lymphocytic leukemia into a high-grade lymphoma. RS occurs in 3% to 10% of chronic lymphocytic leukemia cases, and its onset is often characterized by the abrupt development of systemic symptoms (eg, fever in the absence of infection, night sweats, and weight loss), progressive lymphadenopathy, and hepatosplenomegaly. RS frequently arises in the lymph nodes or bone marrow, and rarely presents with extranodal involvement, which includes the gastrointestinal tract, eye, testis, central nervous system, lung, kidney, and skin. We review the literature regarding the clinical course and treatment of RS, present a patient with primary cutaneous RS, and discuss the prognostic implications.
American Academy of Dermatology
Richter syndrome: a review of clinical, ocular, neurological and other manifestations.
Br J Haematol. 2008 Sep
Omoti CE, Omoti AE.
Department of Haematology, University of Benin Teaching Hospital, Benin City, Nigeria. ediomoti@yahoo.com
Richter syndrome describes the development of high-grade non-Hodgkin lymphoma (NHL) or Hodgkin lymphoma in patients with chronic lymphocytic leukemia (CLL)/small lymphocytic lymphoma (SLL). Richter transformation occurs in 3.3 to 10.6% of patients with CLL. The large cell lymphoma clone occurs by transformation of the original CLL clone in the majority of patients, and as a separate and independent neoplasm in fewer cases. Richter transformation may be triggered by viral infections, such as Epstein-Barr virus infection, which are common in immunosuppressed patients. Trisomy 12 and chromosome 11 abnormalities, as well as multiple genetic defects, have been described in patients with Richter syndrome.
These abnormalities may cause CLL cells to proliferate and, by facilitating the acquisition of new genetic abnormalities, to transform into Richter syndrome cells. Presenting features typically include a rapid clinical deterioration with fever in the absence of infection, progressive lymph node enlargement, and an elevation in serum lactate dehydrogenase. Extranodal Richter syndrome has also been reported to occur in the central nervous system, eye, gastrointestinal system, nose, skin, face, bone and bronchus.
The therapeutic options include cytoreductive therapy consisting of chemotherapy and immunotherapy, followed by allogeneic stem cell transplantation as postremission therapy.
Richter syndrome: biology, incidence, and therapeutic strategies.
Tsimberidou AM, Keating MJ.
Department of Leukemia, The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030, USA. atsimber@mdanderson.org
Richter’s transformation denotes the development of high-grade non-Hodgkin lymphoma, prolymphocytic leukemia, Hodgkin disease, or acute leukemia in patients with chronic lymphocytic leukemia (CLL)/small lymphocytic lymphoma. A search of published articles in Medline (PubMed) and abstracts from professional meetings was performed. An electronic database search of patients with CLL at The University of Texas M. D. Anderson Cancer Center (Houston, TX) determined the incidence of Richter syndrome (RS) in patients with CLL between 1992 and 2002. RS occurs in approximately 5% of patients with CLL. The large cells of RS may arise through transformation of the original CLL clone or represent a new neoplasm. RS may be triggered by viral infections, such as Epstein-Barr virus.
Trisomy 12 and chromosome 11 abnormalities are more frequent in patients with RS than in the overall population of patients with CLL. Multiple genetic defects, such as mutations of the p53 tumor suppressor gene, p16INK4A, and p21, loss of p27 expression, deletion of retinoblastoma, increased copy number of C-MYC, and decreased expression of the A-MYB gene, have been described. These abnormalities may cause CLL cells to proliferate and-by facilitating the acquisition of new genetic abnormalities-to transform into RS cells.
Therapeutic strategies include intensive chemotherapy, monoclonal antibodies, and stem cell transplantation. The response rates range from 5% to 43% (complete response, 5-38%), and the median survival duration ranges from 5 months to 8 months. In conclusion, RS may be triggered by viral infections or by genetic defects. Current treatments are aggressive, but prognosis is poor. Novel curative treatment strategies are needed. (c) 2004 American Cancer Society
The lymphatic system in health and disease.
Cueni LN, Detmar M.
Institute of Pharmaceutical Sciences, Swiss Federal Institute of Technology, ETH Zurich, Zurich, Switzerland.
Abstract
The lymphatic vascular system has an important role in the regulation of tissue pressure, immune surveillance and the absorption of dietary fat in the intestine. There is growing evidence that the lymphatic system also contributes to a number of diseases, such as lymphedema, cancer metastasis and different inflammatory disorders. The discovery of various molecular markers allowing the distinction of blood and lymphatic vessels, together with the availability of a increasing number of in vitro and in vivo models to study various aspects of lymphatic biology, has enabled tremendous progress in research into the development and function of the lymphatic system.
This review discusses recent advances in our understanding of the embryonic development of the lymphatic vasculature, the molecular mechanisms mediating lymphangiogenesis in the adult, the role of lymphangiogenesis in chronic inflammation and lymphatic cancer metastasis, and the emerging importance of the lymphatic vasculature as a therapeutic target.
Lyme Disease
Borrelia burgdorferi
What is Lyme disease? (1)
Lyme disease is a bacterial disease caused by Borrelia burgdorferi (boar-ELL-ee-uh burg-dorf-ERR-eye). Within 1 to 2 weeks of being infected, people may have a “bull’s-eye” rash with fever, headache, and muscle or joint pain. Some people have Lyme disease and do not have any early symptoms. Other people have a fever and other “flu-like” symptoms without a rash.
After several days or weeks, the bacteria may spread throughout the body of an infected person. These people can get symptoms such as rashes in other parts of the body, pain that seems to move from joint to joint, and signs of inflammation of the heart or nerves. If the disease is not treated, a few patients can get additional symptoms, such as swelling and pain in major joints or mental changes, months after getting infected.
Can animals transmit Lyme disease to me?
Yes, but not directly. People get Lyme disease when they are bitten by ticks carrying B. burgdorferi. Ticks that carry Lyme disease are very small and can be hard to see. These tiny ticks bite mice infected with Lyme disease and then bite people or other animals, such as dogs and horses, passing the disease to them.
How can I protect myself from Lyme disease?
Whenever possible, you should avoid entering areas that are likely to be infested with ticks, particularly in spring and summer when nymphal ticks feed.
If you are in an area with ticks, you should wear light-colored clothing so that ticks can be spotted more easily and removed before becoming attached.
If you are in an area with ticks, wear long-sleeved shirts, and tuck your pants into socks. You may also want to wear high rubber boots (since ticks are usually located close to the ground).
Application of insect repellents containing DEET (n,n-diethyl-m-toluamide) to clothes and exposed skin, and permethrin (which kills ticks on contact) to clothes, should also help reduce the risk of tick attachment. DEET can be used safely on children and adults but should be applied according to Environmental Protection Agency guidelines to reduce the possibility of toxicity.
Since transmission of B. burgdorferi from an infected tick is unlikely to occur before 36 hours of tick attachment, check for ticks daily and remove them promptly. Embedded ticks should be removed by using fine-tipped tweezers. Cleanse the area with an antiseptic.
You can reduce the number of ticks around your home by removing leaf litter, and brush- and wood-piles around your house and at the edge of your yard. By clearing trees and brush in your yard, you can reduce the likelihood that deer, rodents, and ticks will live there.
How can I find more information about Lyme disease?
Learn more about Lyme disease, including answers to frequently asked questions, the natural history of Lyme disease and a narrated documentary, at CDC’s Lyme disease web site.
The Lyme disease bacterium, Borrelia burgdorferi, normally lives in mice, squirrels and other small animals. It is transmitted among these animals – and to humans – through the bites of certain species of ticks. In the northeastern and north-central United States, the black-legged tick (or deer tick, Ixodes scapularis) transmits Lyme disease. In the Pacific coastal United States, the disease is spread by the western black-legged tick (Ixodes pacificus). Other major tick species found in the United States have not been shown to transmit Borrelia burgdorferi.
Symptoms of Lyme Disease:
Lyme disease is a bacterial infection that features a skin rash, swollen joints and flu-like symptoms. You get the disease from the bite of an infected tick. Sometimes it is hard to know if you have Lyme disease because you may not have noticed a tick bite. Also, many of its symptoms are like those of other diseases. Symptoms may include:
In the early stages, doctors look at your symptoms and medical history to figure out whether you have Lyme disease. In the later stages of the disease, lab tests can confirm whether you have it. (2)
Additional Information on Symptoms (3)
Typically, the first symptom of Lyme disease is a red rash known as erythema migrans (EM). The telltale rash starts as a small red spot at the site of the tick bite and expands over time, forming a circular or oval-shaped rash. As infection spreads, rashes can appear at different sites on the body. Erythema migrans is often accompanied by symptoms such as fever, headache, stiff neck, body aches, and fatigue.
After several months of B. Burgdorferi infection, slightly more than half of people not treated with antibiotics develop recurrent attacks of painful and swollen joints, most commonly in the knees. About 10 to 20 percent of untreated people develop chronic arthritis.
Lyme disease can also affect the nervous system, causing such symptoms as stiff neck, Bell’s palsy, and numbness in the limbs. Less commonly, untreated people can develop heart problems, hepatitis, and severe fatigue.
Lyme Disease Diagnosis
Lyme disease is diagnosed based on symptoms, objective physical findings (such as erythema migrans, facial palsy, or arthritis), and a history of possible exposure to infected ticks. Validated laboratory tests can be very helpful but are not generally recommended when a patient has erythema migrans.
When making a diagnosis of Lyme disease, health care providers should consider other diseases that may cause similar illness. Not all patients with Lyme disease will develop the characteristic bulls-eye rash, and many may not recall a tick bite. Laboratory testing is not recommended for persons who do not have symptoms of Lyme disease.
Laboratory Testing
Several forms of laboratory testing for Lyme disease are available, some of which have not been adequately validated. Most recommended tests are blood tests that measure antibodies made in response to the infection. These tests may be falsely negative in patients with early disease, but they are quite reliable for diagnosing later stages of disease.
CDC recommends a two-step process when testing blood for evidence of Lyme disease. Both steps can be done using the same blood sample.
1) The first step uses an ELISA or IFA test. These tests are designed to be very “sensitive,” meaning that almost everyone with Lyme disease, and some people who don’t have Lyme disease, will test positive. If the ELISA or IFA is negative, it is highly unlikely that the person has Lyme disease, and no further testing is recommended. If the ELISA or IFA is positive or indeterminate (sometimes called “equivocal”), a second step should be performed to confirm the results.
The second step uses a Western blot test. Used appropriately, this test is designed to be “specific,” meaning that it will usually be positive only if a person has been truly infected. If the Western blot is negative, it suggests that the first test was a false positive, which can occur for several reasons. Sometimes two types of Western blot are performed, “IgM” and “IgG.” Patients who are positive by IgM but not IgG should have the test repeated a few weeks later if they remain ill. If they are still positive only by IgM and have been ill longer than one month, this is likely a false positive.
CDC does not recommend testing blood by Western blot without first testing it by ELISA or IFA. Doing so increases the potential for false positive results. Such results may lead to patients being treated for Lyme disease when they don’t have it and not getting appropriate treatment for the true cause of their illness. For detailed recommendations for test performance and interpretation of serologic tests for Lyme disease,
Other Types of Laboratory Testing
Some laboratories offer Lyme disease testing using assays whose accuracy and clinical usefulness have not been adequately established. These tests include urine antigen tests, immunofluorescent staining for cell wall-deficient forms of Borrelia burgdorferi, and lymphocyte transformation tests. In general, CDC does not recommend these tests. Click here for more information. Patients are encouraged to ask their physicians whether their testing for Lyme disease was performed using validated methods and whether results were interpreted using appropriate guidelines.
Testing Ticks
Patients who have removed a tick often wonder if they should have it tested. In general, the identification and testing of individual ticks is not useful for deciding if a person should get antibiotics following a tick bite. Nevertheless, some state or local health departments offer tick identification and testing as a community service or for research purposes. Check with your health department; the phone number is usually found in the government pages of the telephone book.Healthcare providers may have difficulty diagnosing Lyme disease because many of its more common symptoms are similar to those of other disorders and viral infections. In addition, the only distinctive sign unique to Lyme disease—the EM rash is absent in at least one-fourth of the people who become infected.
Complications of Lyme Disease
Left untreated, Lyme disease can cause: (5)
Treatments and drugs (5)
Oral antibiotics
Oral antibiotics are the standard treatment for early-stage Lyme disease. These usually include doxycycline for adults and children older than 8, or amoxicillin or cefuroxime axetil for adults, younger children and pregnant or breast-feeding women. These drugs often clear the infection and prevent complications. A 14- to 21-day course of antibiotics is usually recommended, but some studies suggest that courses lasting 10 to 14 days are equally effective. In some cases, longer treatment has been linked to serious complications.
Intravenous antibiotics
If the disease has progressed, your doctor may recommend treatment with an intravenous antibiotic for 14 to 28 days. This is effective in eliminating infection, although it may take some time to recover symptomatically. Intravenous antibiotics can cause various side effects, including a lower white blood cell count, gallstones and mild to severe diarrhea.
Avoid bismacine
The Food and Drug Administration (FDA) warns consumers and health care providers to avoid bismacine, an injectable compound prescribed by some alternative medicine practitioners to treat Lyme disease. Bismacine, also known as chromacine, contains high levels of the metal bismuth. Although bismuth is safely used in some oral medications for stomach ulcers, it’s not approved for use in injectable form or as a treatment for Lyme disease. Bismacine can cause bismuth poisoning, which may lead to heart and kidney failure.
Chronic Lyme Disease
What is “chronic Lyme disease”?
Lyme disease is an infection caused by the bacterium Borrelia burgdorferi. In the majority of cases, it is successfully treated with oral antibiotics.
Chronic Lyme disease (CLD) is a controversial term applied to a broad spectrum of patients, including individuals with Lyme disease, those with post Lyme disease syndrome (PLDS), as well as patients with no evidence of current or past B. burgdorferi infection. (Infect Dis Clin N Am 2008; 22:341-60). It is often used to describe a poorly defined group of illnesses characterized by a broad range of symptoms that often include, but are not limited to, chronic fatigue, pain, and neurocognitive disorders.
Contrary to the name, however, and despite extensive study, no clear evidence has emerged to support the contention that CLD results from a past or persistent Lyme disease infection. For that reason, experts in this field do not support a diagnosis of CLD, and a recent medical appraisal of CLD concluded that the term is a misnomer (New Eng. J. Med. 2008; 357:1422-30). (4)
American dog tick (Dermacentor variabilis) as well as the Rocky Mountain wood tick (Dermacentor andersoni) can transmit many diseases including Rocky Mountain spotted fever and tularemia.
Blacklegged (or deer) ticks (Ixodes scapularis and Ixodes pacificus) can transmit several tick-borne diseases including anaplasmosis, babesiosis and Lyme disease. An adult tick is pictured at left, though it is the smaller nymphal stage ticks which most commonly bite humans.
Lone star ticks (Amblyomma americanum) have been linked to transmission of ehrlichiosis, tularemia, and southern tick-associated rash illness (STARI). The saliva of these ticks is irritating, and can cause an allergic reaction at the site of the bite
This image shows the stages and relative sizes of these tick species. Only the blacklegged ticks are known to transmit Lyme disease.
References:
(1) National Center for Infectious Diseases
(2) Medline Plus
(3) National Institutes of health
(5) Mayo Clinic
Tularemia
Francisella tularensis bacterium
What is Tularemia?
Tularemia is a potentially serious illness that occurs naturally in the United States. It is caused by the bacterium Francisella tularensis found in animals (especially rodents, rabbits, and hares).
Categories of tularemia(2)
Some authorities classify tularemia into 2 groups, which include the far more common ulceroglandular form (in which local or regional symptoms and signs predominate) and the more lethal typhoidal form (in which systemic symptoms dominate the clinical picture). More commonly, however, tularemia is divided into 6 forms:
Ulceroglandular
Glandular
Oculoglandular
Oropharyngeal
Pneumonic
Typhoidal
What are the Symptoms of Tularemia?
Symptoms of tularemia could include:
sudden fever
chills
headaches
diarrhea
muscle aches
joint pain
dry cough
progressive weakness
enlarged lymph nodes (lymphandeonopathy)
People can also catch pneumonia and develop chest pain, bloody sputum and can have trouble breathing and even sometimes stop breathing.
Other symptoms of tularemia depend on how a person was exposed to the tularemia bacteria. These symptoms can include ulcers on the skin or mouth, swollen and painful lymph glands, swollen and painful eyes, and a sore throat.
How is Tularemia Diagnosed?
Tests and Exams include:
Serology for tularemia
PCR (polymerase chain reaction) test of a sample from an ulcer
Blood culture for tularemia
Chest x-ray
This disease may also alter the results of febrile/cold agglutinins.
How Does Tularemia Spread?
People can get tularemia many different ways:
being bitten by an infected tick, deerfly or other insect
handling infected animal carcasses
eating or drinking contaminated food or water
breathing in the bacteria, F. tularensis
Tularemia is not known to be spread from person to person. People who have tularemia do not need to be isolated. People who have been exposed to the tularemia bacteria should be treated as soon as possible. The disease can be fatal if it is not treated with the right antibiotics.
How Soon Do Infected People Get Sick?
Symptoms usually appear 3 to 5 days after exposure to the bacteria, but can take as long as 14 days.
Possible Complications of Tularemia (1)
Meningitis. This is a serious and sometimes life-threatening infection of the fluid and membranes (meninges) surrounding the brain and spinal cord. Signs and symptoms of bacterial meningitis include a high fever, severe headache, stiff neck and sensitivity to light. If not treated promptly, bacterial meningitis can cause brain damage and even death.
Pericarditis. This is swelling and irritation of the pericardium, the thin membrane that surrounds the heart. Mild pericarditis often improves without treatment, but more serious cases may require antibiotic therapy.
Bone infection (osteomyelitis). Tularemia bacteria sometimes spread to the bones, leading to pain, decreased range of motion in nearby joints, and sometimes to skin redness, tenderness or open sores in the affected areas.
Pneumonia Pneumonia is an infection of the lungs. Many different organisms can cause it, including bacteria, viruses, and fungi.Pneumonia can range from mild to severe, and can even be deadly. The severity depends on the type of organism causing pneumonia, as well as your age and underlying health.
What Should I Do if I Think I Have Tularemia?
Consult your doctor at the first sign of illness. Be sure to let the doctor know if you are pregnant or have a weakened immune system.
How Is Tularemia Treated?
Your doctor will most likely prescribe antibiotics, which must be taken according to the directions supplied with your prescription to ensure the best possible result. Let your doctor know if you have any allergy to antibiotics. Antibiotics used include streptomycin or gentamicin, which are given by injection directly into a muscle or vein and Streptomycin and tetracycline which are also commonly used.
A vaccine for tularemia is under review by the Food and Drug Administration and is not currently available in the United States.
What Can I Do To Prevent Becoming Infected with Tularemia?
Tularemia occurs naturally in many parts of the United States. Use insect repellent containing DEET on your skin, or treat clothing with repellent containing permethrin, to prevent insect bites. Wash your hands often, using soap and warm water, especially after handling animal carcasses. Be sure to cook your food Note any change in the behavior of your pets (especially rodents, rabbits, and hares) or livestock, and consult a veterinarian if they develop unusual symptoms.
Also (Illinois Dept of Public Health)
What can be done to prevent the spread of tularemia?
Several precautions can protect individuals from tularemia.
How should an attached tick be removed?
Remove any tick promptly. Do not try to burn the tick with a match or cover it with petroleum jelly or nail polish. Do not use bare hands. The best way to remove a tick is to grasp it with fine-point tweezers as close to the skin as possible and gently, but firmly, pull it straight out. Do not twist or jerk the tick. If tweezers are not available, grasp the tick with a piece of cloth or whatever can be used as a barrier between your fingers and the tick. You may want to put the tick in a jar of rubbing alcohol labeled with the date and location of the bite in case you seek medical attention and your physician wishes to have the tick identified.
The mouthparts of a tick are shaped like tiny barbs and may remain embedded and lead to infection at the bite site if not removed properly. Be sure to wash the bite area and your hands thoroughly with soap and water, and apply an antiseptic to the bite site.
*
Can Tularemia Be Used As a Weapon?
Francisella tularensis is very infectious. A small number (10-50 or so organisms) can cause disease. If F. tularensis were used as a weapon, the bacteria would likely be made airborne for exposure by inhalation. People who inhale an infectious aerosol would generally experience severe respiratory illness, including life-threatening pneumonia and systemic infection, if they are not treated. The bacteria that cause tularemia occur widely in nature and could be isolated and grown in quantity in a laboratory, although manufacturing an effective aerosol weapn would require considerable sophistication.
What is CDC Doing About Tularemia?
The CDC operates a national program for bioterrorism preparedness and response that incorporates a broad range of public health partnerships. Other things CDC is doing include:
Stockpiling antibiotics to treat infected people
Coordinating a nation-wide program where states share information about tularemia
Creating new education tools and programs for health professionals, the public, and the media.
For more information, visit www.bt.cdc.gov/agent/tularemia, or call the CDC public response hotline at (800) CDC-INFO (English), (888) 246-2857 (Español), or (888) 232-6348 (TTY).
References:
2.) EMedicine
Lymphogranuloma Venereum (LGV)
A previously little known sexually transmitted disease (STD) lymphogranuloma venereum is on the rapid rise according to the CDC. The CDC also classifies it as a new “emerging” disease.This infection which can seriously effect the lymph nodes is endemic in Africa, the Caribbean, South America and South-east Asia. In the West, its rise has been sudden and until very recently not well tracked.
What is lymphogranuloma venereum (LGV)?
LGV is a sexually transmitted disease (STD) or infection involving the lymph glands in the genital area. It is caused by a specific strain of Chlamydia.
Who gets LGV?
The incidence is highest among sexually active people living in tropical or subtropical climates. It has also occurred in some areas of the southern United States.
How is LGV spread?
The infection is spread by sexual contact.
What are the symptoms of LGV?
The first symptom may be a small, painless pimple or lesion occurring on the penis or vagina. It is often unnoticed. The infection then spreads to the lymph nodes in the groin area and from there to the surrounding tissue. Complications may include inflamed and swollen lymph glands which may drain and bleed.
How soon do symptoms appear?
The onset of symptoms varies widely. The initial lesion may appear from three to 30 days after exposure.
When and for how long is a person able to spread LGV?
An individual remains infectious as long as there are active lesions.
What is the treatment for LGV?
Treatment involves the use of certain antibiotics, specifically tetracycline or sulfamethoxazole.
What can be done to prevent the spread of LGV?
There are a number of ways to prevent the spread of LGV:
Limit your number of sex partners.
Use a male or female condom.
Carefully wash genitals after sexual relations.
If you think you are infected, avoid any sexual contact and visit your local STD clinic, a hospital or your doctor.
Notify all sexual contacts immediately so they can obtain examination and treatment.
Lymphogranuloma Venereum
Synonyms: LGV, Durand-Nicholas-Favre’s disease, lymphopatia venereum, lymphogranuloma inguinale, tropical bubo, poradenitis inguinales
Description
This disease is due to infection with the L1, L2 or L3 serovars of Chlamydia trachomatis.
Unlike genitourinary chlamydial infection which infects squamocolumnar epithelial cells, these serovars cause infection of mononuclear phagocytes in the lymphatic system.
The disease was largely confined to tropical regions of the world, but there are now outbreaks arising locally in Europe (particularly The Netherlands) and America, predominantly affecting men who have sex with men. This was largely rectal infection presenting with proctitis.1
Cases in the developed world are largely due to the L2 serovar.
Epidemiology
The disease is endemic in East and West Africa, India, The Caribbean, South America and South-East Asia.2
There are no reliable figures for population prevalence.
In India and Africa it accounts for 2–10% of genital ulcer disease.
The Health Protection Agency recently launched a case ascertainment and awareness initiative and >100 cases occurred in the UK during the first half of 2005. Subsequent studies have revealed that the number of cases have now reduced to 12 per month (32 per month back in 2005).3,4
These were largely confined to the metropolitan London area and Brighton, but smaller clusters have occurred in other areas.
Risk factors
Unprotected sexual intercourse2
Receptive anal intercourse
Sexual contacts in endemic areas
Prostitution
Multiple sexual partners5
Male gender
Anal enema use6
Presentation
The clinical presentation is divided into primary, secondary and tertiary patterns.
Primary LGV
Primary LGV presentation is seen in about one third of infected men, but rarely in women.
Occurs 3 days to 3 weeks after exposure.2
Usually present with painless papule or shallow ulcer/erosion.
May be groups of lesions resembling herpes infection.
Symptoms of urethritis may occur.
In men it is usually the coronal sulcus, frenulum, penile shaft, foreskin, glans, scrotum, urethra or anus that are affected.
Men may develop a penile lymphangitis of the dorsal penile shaft, with cord-like thickening.
A tender nodule may form in the regional lymph glands which can undergo rupture or sinus formation.
When women do display symptoms of primary LGV, it affects the posterior vaginal wall, posterior lip of cervix, vulva and fourchette.
Oral cases may occur in men and women following oral sexual intercourse.
Secondary LGV
Usually occurs 10–30 days after exposure but may take several months to develop.
Buboes (grossly enlarged tender nodes) form in the regional lymph drainage.
There may be symptoms of systemic illness such as fever, headache, nausea, vomiting, lethargy and arthralgia.
Buboes affect either the inguinal, pelvic or perirectal lymph nodes, depending on the original site of genital infection and may be unilateral or bilateral.
If oral infection occurs then the submaxillary and cervical lymph glands are affected.
The groove sign may occur, particularly in men, due to separation of the enlarged inguinal and femoral lymph nodes by the inguinal ligament. This sign is present in about a fifth of male cases. However, it has also been associated with non-Hodgkin’s lymphoma.7
There is usually erythema and induration of skin overlying the enlarged nodes and there may be rupture of the buboes with sinus or fistula formation
.
The skin may be affected by erythema multiforme, urticaria, erythema nodosum or scarlatiniform rash.
Rarely there may be signs of conjunctivitis, hepatomegaly, meningoencephalitis, pericarditis, pneumonia and arthritis.
Tertiary LGV
This late presentation can occur up to 20 years after infection.
There is usually proctocolitis, which can be confused with other causes of distal colonic inflammation.
Patients may complain of anal itching, bloody mucopurulent anal discharge, rectal pain and tenesmus, passage of very thin stools with constipation or weight loss.
Swollen haemorrhoid-like structures, due to lymphatic obstruction, may be seen at the rectal margin.
Digital rectal examination or proctoscopy may reveal a granular mucosa and enlarged nodes beneath it.
There may be rectal fibrosis and stricture in advanced cases (reversible with treatment)8 and elephantiasis of the genitals in men.
Esthiomene – an ‘eating away’ of the genitalia may affect women. There is chronic hypertrophy and granulomatous enlargement of the vulva with ulceration and erosion.
Differential diagnosis
Depends on the stage of disease.
Primary and secondary disease resembles
Syphilis
Genital herpes
Cat scratch disease (Bartonella henselae infection)
Chancroid (Haemophilus ducreyi – another tropical STI)
Donovanosis, aka granuloma inguinale (Calymmatobacterium granulomatis – another tropical STI)
Bubonic plague
Mycobacterial infections
Tularaemia
Malignant causes of lymphadenopathy, e.g. Hodgkin’s disease
Anogenital syndrome
Anal/rectal carcinoma
Actinomycosis
Schistosomiasis
Lymphatic filariasis
Mycosis
Investigations
Other causes of inguinal lymphadenopathy and genital ulceration must be considered and ruled out.
Full screening for sexually transmitted infections should be carried out if possible, preferably via genitourinary medicine clinic.2
Samples for culture or analysis may be collected from percutaneous drainage of buboes, or from exudate of ulcer base or rectal tissue.
Complement fixation (CF) test has sensitivity of 80%, with cross-reactivity with other chlamydial species and serovars.
A microimmunofluorescence test for the L serovars of C. trachomatis has higher sensitivity and specificity than CF test.
Polymerase chain reaction assays have highest specificity and sensitivity and are increasingly being used to reach a definitive diagnosis.9
CT imaging may be used to assess extent of lymphadenopathy and look for alternative causes.
Sigmoidoscopy/colonoscopy with tissue biopsy may be needed to diagnose the cause of anorectal symptoms. Tissue histology can be non-specific.
Management
Medical therapy
First-line treatment is usually with doxycycline 100 mg twice daily for 21 days, or erythromycin 500 mg 4 times daily for the same period.10 Protocols using doxycycline are successful both in those who are and are not co-infected with HIV.11
Tetracycline or minocycline may also be used. Azithromycin may be given 1g weekly for 3 weeks and appears to be effective.
This regimen has recently been reviewed and there is no current evidence for it to be altered.11
Surgical therapy
Buboes may be drained percutaneously to relieve symptoms.
Surgical excision is best avoided due to risk of sinus or fistula formation.
Other therapy
Patient should refrain from unprotected sexual intercourse until they and any contacts have completed treatment and follow-up.
Monitoring
Follow-up after 3 weeks with testing to look for evidence of cure may be needed.
Patients with rectal stricture or other advanced complications may require surgical intervention.
Prognosis
If diagnosed in primary/secondary stage, full cure is expected with appropriate antibiotic therapy.2
Tertiary cases may have long-term complications despite bacteriological cure.
Infection provides no significant immunity to future re-infection, and relapse of infection after treatment may occur in some cases.
Complications
Bubo rupture with sinus or fistula formation
Fibrosis/deformation of penis
Cervicitis or salpingitis in women
Colonic obstruction due to rectal stricture
Conjunctivitis
Arthritis
Pericarditis
Pneumonia
Meningoencephalitis
Hepatomegaly
Prevention
Awareness of disease in developed world
Surveillance and testing in GUM clinics/opportunistically in primary care
Practice of safe sex
Contact tracing of confirmed cases, where possible
