Indian J Sex Transm Dis Indian J Sex Transm Dis
Official Publication of the Indian Association for the Study of Sexually Transmitted Disesses
Indian J Sex Transm Dis
The Journal | Search | Ahead Of Print | Current Issue | Archives | Instructions | Subscribe | Login    Users online: 11   Home Email this page Print this page Bookmark this page Decrease font size Default font size Increase font size


 
  Table of Contents  
LETTER TO EDITOR
Year : 2012  |  Volume : 33  |  Issue : 1  |  Page : 62-64
 

Diffuse cutaneous leishmaniasis - A rare cutaneous presentation in an HIV-positive patient


Centre of Excellence, Antiretroviral Therapy Centre, Room No. 201-202, O.P.D. Building, B.J. Medical College and Civil Hospital, Ahmedabad, Gujarat, India

Date of Web Publication14-Mar-2012

Correspondence Address:
Hemang M Purohit
Centre of Excellence, Antiretroviral Therapy Centre, Room No. 201-202, O.P.D. Building, B.J. Medical College and Civil Hospital, Ahmedabad, Gujarat - 380 016
India
Login to access the Email id


DOI: 10.4103/0253-7184.93834

PMID: 22529461

Get Permissions

 



How to cite this article:
Purohit HM, Shah AN, Amin BK, Shevkani MR. Diffuse cutaneous leishmaniasis - A rare cutaneous presentation in an HIV-positive patient. Indian J Sex Transm Dis 2012;33:62-4

How to cite this URL:
Purohit HM, Shah AN, Amin BK, Shevkani MR. Diffuse cutaneous leishmaniasis - A rare cutaneous presentation in an HIV-positive patient. Indian J Sex Transm Dis [serial online] 2012 [cited 2014 Nov 21];33:62-4. Available from: http://www.ijstd.org/text.asp?2012/33/1/62/93834


Sir,

Leishmaniasis is a vector-borne disease that is transmitted by sandflies and caused by obligate intracellular protozoa of the genus Leishmania. Leishmaniasis occurs in four different forms of diseases known as visceral leishmaniasis, or kala-azar, cutaneous leishmaniasis, mucocutaneous leishmaniasis, and diffuse cutaneous leishmaniasis. [1] We present this case because of widespread mucocutaneous lesions noticed in an HIV-infected patient, which was initially misunderstood as histoplasmosis but was later correctly diagnosed as diffuse cutaneous leishmaniasis and treated accordingly. Very few such cases were reported in Indian context.

A 33-year-old HIV positive male from Jodhpur, Rajasthan, rickshaw/truck driver by profession presented at Department of Dermatology, Civil Hospital, Ahmedabad, with extensive skin lesions. He had complaint of fatigue, recurrent diarrhea, and weight loss. On careful history taking he reported to have multiple unprotected sexual exposures. There was no past history of any prolonged fever with hepatosplemomegaly suggestive of kala-azar.

Our case had multiple widespread infiltrated papulonodular lesions (>200) over the skin, nasal, and oral mucosa. In the present case, post-kala-azar dermal leishmaniasis was ruled out as our patient hailed from an area nonendemic for kala-azar.

For HIV infection patient was on stavudine+lamivudine+nevirapine (baseline cd4-201) since 2004 along with septran prophylaxis under the National AIDS Control Program since 18 months from ART Centre, Jodhpur, Rajasthan. He was referred to our ART Centre for further management of HIV infection [Figure 1].
Figure 1: Cutaneous lesions. Patient showing cutaneous lesions on face and body, specially note the lesions on nasal and beard area

Click here to view


At our ART Centre, CD4 was 95. Other investigations: Complete blood counts, liver function tests, and renal function tests reported within normal limits. Serological tests for hepatitis B and hepatitis C virus was nonreactive. Serum lactate dehydrogenase (LDH) was raised (308 U/L) and serum ferritin was normal (151 ng/ml).

Microscopic examinations of skin smear using giemsa staining revealed exta- and intracellular leishman bodies. Skin biopsy revealed a massive dermal histolytic infiltration with round cytoplasmic microgranules 1-2 μ in diameter. Elisa test for Leishmania donovani antigen and antibody detection was negative.

Bone marrow biopsy examination report commented as "bone marrow studded with plenty of intracellular as well as extracellular amastigote forms of leishmania organisms having two dots - kinetoplast and nuclei" and also confirmed no evidence of any primary hematological malignancy or marrow infiltration by lymphoma [Figure 2]. Polymerase chain reaction method has the potential to become technique of choice for diagnosis of cutaneous leishmaniasis, but in our case we could not perform it. [2] However, it was not much clear whether this infection is a case of opportunistic infection or immune reconstitution inflammatory syndrome. In India, CL is commonly seen in states of Rajasthan, Bihar, West Bengal, and Orissa; therefore, endemicity of the disease must be taken into consideration for diagnosis. [3]
Figure 2: LD bodies. Bone marrow smear stained with Giemsa stain showing intracellular Leishmania donovani amastigote forms stained red-violet kinetoplast with pale cytoplasm

Click here to view


Patient was treated with ketoconazole 200 mg twice daily and rifamycin 450 mg daily. He was referred to Medicine Department, where he was admitted. Multifosine is drug of choice, but due to unavailability he was put on pentavalent antimony compounds - sodium stibogluconate. [4] The drug appears to inhibit amastigote glycolytic activity and fatty acid oxidation. Literature also suggests use of alternative drugs such as amphotericin B, metronidazole, levamisole, and dapsone. [5]

Response to antimony compounds was seen in terms of decrease in size and number of lesions. But he developed jaundice as a complication of the treatment. Later on patient took discharge on request. He was advised recommended course of treatment and given follow-up in OPD but he never returned. On tracking through ART centre, we found he expired. Cutaneous leishmaniasis and HIV infection as management of such condition are crucial compared to immunocompetent patient.


   Acknowledgment Top


The authors would like to thank Dr. B. D. Mankad (Ex. Nodal Officer), Dr. Umesh Nihalani (Senior Medical Officer) and Dr. Burzin Kavina (Research Officer) at ART Centre of the Institute for their help in collecting the detail history of the patient and manuscript preparation. We are also thankful to Skin Department of our Institute.

 
   References Top

1.Shah S, Shah A, Prajapati S, Bilimoria F. Post-kala-azar dermal leishmaniasis in HIV-positive patients: A study of two cases. Indian J Sex Transm Dis 2010;31:42-4.  Back to cited text no. 1
[PUBMED]  Medknow Journal  
2.Al-Mutairi N, Alshiltawy M, El Khalawany M, Joshi A, Eassa BI, Manchanda Y, et al. Treatment of old world cutaneous leishmaniasis with dapsone, itraconazole, cryotherapy, and imiquimod, alone and in combination. Int J Dermatol 2009;48:862-9.  Back to cited text no. 2
[PUBMED]  [FULLTEXT]  
3.Singh S, Sivakumar R. Recent advances in the diagnosis of leishmaniasis. J Postgrad Med 2003;49:56-60.  Back to cited text no. 3
    
4.Choi CM, Lerner EA. Leishmaniasis as an emerging infection. J Investig Dermatol Symp Proc 2001;6:175-182.  Back to cited text no. 4
[PUBMED]    
5.Herwaldt BL. Leishmaniasis. In Harrison's Principles of Internal Medicine - Vol. 1, 17 th ed. New York: Mc Graw Hill Companies Inc.; 2008. p. 1296-300.  Back to cited text no. 5
    


    Figures

  [Figure 1], [Figure 2]


This article has been cited by
1 Changing trends in the epidemiology, clinical presentation, and diagnosis of Leishmania–HIV co-infection in India
Sarman Singh
International Journal of Infectious Diseases. 2014;
[Pubmed]



 

Top
Print this article  Email this article
 

    

 
  Search
 
  
 
    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
    Article in PDF (708 KB)
    Citation Manager
    Access Statistics
    Reader Comments
    Email Alert *
    Add to My List *
* Registration required (free)  


   Acknowledgment
    References
    Article Figures

 Article Access Statistics
    Viewed2074    
    Printed48    
    Emailed0    
    PDF Downloaded66    
    Comments [Add]    
    Cited by others 1    

Recommend this journal