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Table. 
Characteristics of Patients Diagnosed as Having Visceral Leishmaniasis
Characteristics of Patients Diagnosed as Having Visceral Leishmaniasis
1.
Wallace  MRHale  BRUtz  GC  et al.  Endemic infectious diseases of Afghanistan. Clin Infect Dis 2002;34 ((suppl 5)) S171- S207
PubMedArticle
2.
Magill  AJ Epidemiology of the leishmaniases. Dermatol Clin 1995;13 (3) 505- 523
PubMed
3.
Wortmann  GSweeney  CHoung  HS  et al.  Rapid diagnosis of leishmaniasis by fluorogenic polymerase chain reaction. Am J Trop Med Hyg 2001;65 (5) 583- 587
PubMed
4.
Chappuis  FMueller  YNguimfack  A  et al.  Diagnostic accuracy of two rK39 antigen-based dipsticks and the formol gel test for rapid diagnosis of visceral leishmaniasis in northeastern Uganda. J Clin Microbiol 2005;43 (12) 5973- 5977
PubMedArticle
5.
Sundar  SMaurya  RSingh  RK  et al.  Rapid, noninvasive diagnosis of visceral leishmaniasis in India: comparison of two immunochromatographic strip tests for detection of anti-K39 antibody. J Clin Microbiol 2006;44 (1) 251- 253
PubMedArticle
6.
Badaro  RJones  TCCarvalho  EM  et al.  New perspectives on a subclinical form of visceral leishmaniasis. J Infect Dis 1986;154 (6) 1003- 1011
PubMedArticle
7.
Pampiglione  SLa Placa  MSchlick  G Studies on Mediterranean Leishmaniasis, I: an outbreak of visceral leishmaniasis in Northern Italy. Trans R Soc Trop Med Hyg 1974;68 (5) 349- 359
PubMedArticle
8.
Pampiglione  SManson-Bahr  PEGiungi  FGiunti  GParenti  ACanestri Trotti  G Studies on Mediterranean leishmaniasis, 2: asymptomatic cases of visceral leishmaniasis. Trans R Soc Trop Med Hyg 1974;68 (6) 447- 453
PubMedArticle
9.
Badaró  RJones  TCLorenco  R  et al.  A prospective study of visceral leishmaniasis in an endemic area of Brazil. J Infect Dis 1986;154 (4) 639- 649
PubMedArticle
10.
Sundar  SRai  M Laboratory diagnosis of visceral leishmaniasis. Clin Diagn Lab Immunol 2002;9 (5) 951- 958
PubMed
11.
Chappuis  FRijal  SSoto  AMenten  JBoelaert  M A meta-analysis of the diagnostic performance of the direct agglutination test and rK39 dipstick for visceral leishmaniasis. BMJ 2006;333 (7571) 723
PubMedArticle
12.
Meyerhoff  A Food and Drug Administration approval of AmBisome (liposomal amphotericin B) for treatment of visceral leishmaniasis. Clin Infect Dis 1999;28 (1) 42- 51
PubMedArticle
13.
Murray  HW Treatment of visceral leishmaniasis in 2004. Am J Trop Med Hyg 2004;71 (6) 787- 794
PubMed
Research Letters
September 24, 2007

Visceral Leishmaniasis: Clinical Observations in 4 US Army Soldiers Deployed to Afghanistan or Iraq, 2002-2004

Arch Intern Med. 2007;167(17):1899-1901. doi:10.1001/archinte.167.17.1899

People who traveled to Central or Southwest Asia in support of Operation Enduring Freedom and Operation Iraqi Freedom may have been exposed to various diseases endemic to this region.1 Some of these conditions have long incubation periods and may not present for weeks or months after travelers have returned to the United States. Among such diseases is visceral leishmaniasis (VL). Visceral leishmaniasis is a chronic systemic disease caused by parasites of the Leishmania donovani–Leishmania infantum complex. It is classically described as a syndrome of fever, progressive spleen and/or liver enlargement, weight loss, pancytopenia, and, if untreated, possible death. Most cases are acquired via the bite of infected female sand flies, but on rare occasions, disease has been acquired by other means, most notably by blood transfusions.2

This case series describes 4 cases of VL and is intended to alert clinicians to the possibility of VL in patients who develop a febrile illness after returning from deployment to Central or Southwest Asia.

Methods

A retrospective review was performed using medical records of patients diagnosed as having VL at the Walter Reed Army Medical Center (WRAMC), a centralized military leishmaniasis treatment center in Washington, DC. Military disease surveillance systems were queried, and it was confirmed that no other cases had been reported in this time interval.

Routine clinical laboratory studies were performed at WRAMC and local military medical facilities. Histopathological samples were reviewed at the Armed Forces Institute of Pathology (AFIP), Washington, DC. Polymerase chain reaction (PCR) assays designed to amplify a portion of the ribosomal RNA gene to detect Leishmania,3 rK39 dipstick assays (Kalazar Detect; InBios, Seattle, Washington),4,5 and Leishmania cultures were performed at the Walter Reed Army Institute of Research (WRAIR), Silver Spring, Maryland. Anti-Leishmania serum indirect fluorescent antibody tests were performed at the Centers for Disease Control and Prevention (CDC), Atlanta, Georgia, with IgG titers of 1:16 or greater considered positive.

Results

The patients were male, aged from 23 to 39 years (Table). One patient was white, and 3 patients were African American. The median time to onset of symptoms after returning to the United States was 6 months (range, 3-9 months) in 3 patients; 1 patient (patient 3) became ill while still in Iraq at 11 months. Two patients acquired their infections in Afghanistan, and 2 were infected in Iraq. Of note, patient 3 denied traveling anywhere outside of “The Green Zone” in Baghdad, Iraq. Despite receiving prevention briefings prior to deployment that reviewed personal protective measures such as the proper wear of clothing and use of insect repellents, permethrin and diethyltoluamide, all patients reported limitations using these measures during their travel.

In all patients, the initial presentation included symptoms of fever, chills, and night sweats; other symptoms included cough, weight loss, anorexia, nausea, abdominal pain, and diarrhea. The median time from onset of symptoms to definitive diagnosis was 6 weeks (range, 4-8 weeks).

Physical examination findings included hepatomegaly or splenomegaly. Laboratory test results demonstrated pancytopenia and elevated liver-associated enzymes. All patients had positive serologic results when tested with the rK39 antibody dipstick assay. Leishmania amastigotes were visualized on histopathological examination of bone marrow samples in 2 patients and in liver biopsy samples from 2 patients whose preceding bone marrow aspirates were negative. In addition, findings from PCR analysis of tissue biopsy samples were positive in 2 patients. This testing was performed on bone marrow biopsy samples first; in 1 patient whose bone marrow sample was negative for Leishmania, the result of subsequent PCR testing of a liver biopsy specimen was positive.

Three patients were treated with liposomal amphotericin B (AmBisome; Gilead Sciences Inc, Deerfield, Illinois), with total dosages ranging from 21 to 30 mg/kg, resulting in a curative response in each. Patient 2 was treated with amphotericin B lipid complex (Abelcet; Enzon Pharma Inc, Indianapolis, Indiana), 5 mg/kg/d for 5 days, with an additional dose on day 10. This patient experienced an initial clinical improvement, but relapsed 4 days later with the return of symptoms including fevers, abdominal fullness, and right upper quadrant tenderness. He was then treated with a 28-day course of sodium stibogluconate (Pentostam; GlaxoSmithKline, Brentford, England) under an Investigational New Drug (IND) protocol.

Comment

Large numbers of Americans have traveled to Central or Southwest Asia during military deployments. Some of these individuals may have been bitten by a female sand fly harboring Leishmania parasites capable of causing VL. The clinical course following infection may be asymptomatic infection, an acute self-limited febrile illness, or a prolonged nonspecific systemic illness that may or may not progress to overt VL.69 All 4 patients in this case series presented with nonspecific symptoms of fever, chills, and night sweats, which led physicians to develop a very broad differential diagnosis that included many diseases other than VL, including malignant tumors. Patients in this series underwent numerous costly, time-consuming, invasive, and noninvasive diagnostic tests, resulting in delays of diagnosis and treatment for several weeks.

The diagnosis of VL should be suspected based on epidemiologic and clinical features including chronic fever, continued weight loss, weakness, hepatosplenomegaly, anemia, leukopenia and hypergammagloblinemia.9 Definitive diagnosis requires tissue biopsy (bone marrow, liver, or spleen) with histological evidence of the nonflagellated amastigote, growth of the promastigote form in culture, or the identification of Leishmania DNA with molecular assays. The sensitivity of these diagnostic methods varies,10 so consultation with expert laboratories may be of assistance.

A relatively new, commercially available, serodiagnostic assay is the rK39 antibody dipstick test. This assay uses the recombinant Leishmania chagasi antigen rk39 to identify the presence of host antibodies to the parasite's dominant, kinesin-like amastigote antigen. A positive result from this immunoassay is highly sensitive and specific for active VL in immunocompetent individuals.4,5,11

The only drug currently approved by the US Food and Drug Administration (FDA) for the treatment of VL is liposomal amphotericin B (AmBisome).12 For immunocompetent patients, the FDA-approved dosage regimen is 3.0 mg/kg/d, to be given on days 1 to 5, 14, and 21. Of note, amphotericin B lipid complex (Abelcet) is not FDA-approved for this indication. When used in 1 patient in this series, as noted previously, it failed as initial therapy. An acceptable alternative treatment option is the pentavalent antimonial drug, sodium stibogluconate (Pentostam),13 which is available under an IND protocol at WRAMC for military patients and from the CDC for civilian patients.

In conclusion, although not a common disease in returning travelers, VL has been diagnosed in 4 American servicemen returning from Central or Southwest Asia. The rK39 serologic test has proven extremely helpful in the evaluation of suspected VL, but confirmation of the diagnosis with parasitological methods (ie, tissue biopsy with histopathologic analysis, culture, or PCR) is considered the standard of care. Clinicians evaluating travelers returning from endemic regions who present with symptoms suggestive of VL are encouraged to contact the CDC (telephone: 770-488-7760) or (for Department of Defense beneficiaries) the Infectious Disease Service at WRAMC (telephone: 202-782-1663) for assistance with the diagnosis and treatment of patients with this disease.

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Article Information

Correspondence: Dr Myles, Division of Retrovirology, Walter Reed Army Institute of Research, 1 Taft Ct, Ste 250, Rockville, MD 20850 (omyles@hivresearch.org).

Author Contributions:Study concept and design: Myles, Wortmann, Cummings, and Gasser. Acquisition of data: Myles, Wortmann, Cummings, Barthel, Patel, Crum-Cianflone, Negin, Weina, Ockenhouse, Joyce, Magill, Aronson, and Gasser. Analysis and interpretation of data: Myles, Wortmann, Cummings, Barthel, Crum-Cianflone, Weina, Magill, Aronson, and Gasser. Drafting of the manuscript: Myles, Wortmann, Patel, Magill, and Gasser. Critical revision of the manuscript for important intellectual content: Myles, Wortmann, Cummings, Barthel, Crum-Cianflone, Negin, Weina, Ockenhouse, Joyce, Magill, Aronson, and Gasser. Administrative, technical, and material support: Myles, Cummings, Patel, Negin, Weina, Ockenhouse, and Aronson. Study supervision: Myles, Wortmann, Crum-Cianflone, Magill, and Gasser.

Financial Disclosure: None reported.

Disclaimer: The opinion or assertions contained herein are the private views of the authors and are not to be construed as official or as reflecting the views of the Departments of the Army, of the Navy or of Defense.

Additional Contributions: We thank all of the individuals involved at the various institutions providing clinical care and diagnostic services for these patients, especially the nursing staff in the infectious disease clinic and medicine ward at Walter Reed Army Medical Center; the diagnostic laboratory staff at the Walter Reed Army Institute of Research and the Armed Forces Institute of Pathology (Ron Neafie, MS, and Peter McEvoy, MD); Barbara Herwaldt, MD, MPH, at the CDC; and the physicians at Landstuhl Army Medical Center, Germany (Fareed Sheikh, MD, Donald Edelheit, MD, James Hu, MD, and Donald Taillon, MD).

References
1.
Wallace  MRHale  BRUtz  GC  et al.  Endemic infectious diseases of Afghanistan. Clin Infect Dis 2002;34 ((suppl 5)) S171- S207
PubMedArticle
2.
Magill  AJ Epidemiology of the leishmaniases. Dermatol Clin 1995;13 (3) 505- 523
PubMed
3.
Wortmann  GSweeney  CHoung  HS  et al.  Rapid diagnosis of leishmaniasis by fluorogenic polymerase chain reaction. Am J Trop Med Hyg 2001;65 (5) 583- 587
PubMed
4.
Chappuis  FMueller  YNguimfack  A  et al.  Diagnostic accuracy of two rK39 antigen-based dipsticks and the formol gel test for rapid diagnosis of visceral leishmaniasis in northeastern Uganda. J Clin Microbiol 2005;43 (12) 5973- 5977
PubMedArticle
5.
Sundar  SMaurya  RSingh  RK  et al.  Rapid, noninvasive diagnosis of visceral leishmaniasis in India: comparison of two immunochromatographic strip tests for detection of anti-K39 antibody. J Clin Microbiol 2006;44 (1) 251- 253
PubMedArticle
6.
Badaro  RJones  TCCarvalho  EM  et al.  New perspectives on a subclinical form of visceral leishmaniasis. J Infect Dis 1986;154 (6) 1003- 1011
PubMedArticle
7.
Pampiglione  SLa Placa  MSchlick  G Studies on Mediterranean Leishmaniasis, I: an outbreak of visceral leishmaniasis in Northern Italy. Trans R Soc Trop Med Hyg 1974;68 (5) 349- 359
PubMedArticle
8.
Pampiglione  SManson-Bahr  PEGiungi  FGiunti  GParenti  ACanestri Trotti  G Studies on Mediterranean leishmaniasis, 2: asymptomatic cases of visceral leishmaniasis. Trans R Soc Trop Med Hyg 1974;68 (6) 447- 453
PubMedArticle
9.
Badaró  RJones  TCLorenco  R  et al.  A prospective study of visceral leishmaniasis in an endemic area of Brazil. J Infect Dis 1986;154 (4) 639- 649
PubMedArticle
10.
Sundar  SRai  M Laboratory diagnosis of visceral leishmaniasis. Clin Diagn Lab Immunol 2002;9 (5) 951- 958
PubMed
11.
Chappuis  FRijal  SSoto  AMenten  JBoelaert  M A meta-analysis of the diagnostic performance of the direct agglutination test and rK39 dipstick for visceral leishmaniasis. BMJ 2006;333 (7571) 723
PubMedArticle
12.
Meyerhoff  A Food and Drug Administration approval of AmBisome (liposomal amphotericin B) for treatment of visceral leishmaniasis. Clin Infect Dis 1999;28 (1) 42- 51
PubMedArticle
13.
Murray  HW Treatment of visceral leishmaniasis in 2004. Am J Trop Med Hyg 2004;71 (6) 787- 794
PubMed
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