Mixed Cutaneous Infection Caused by Leishmania and Dermatophytes: A Rare Coincidence or Immunological Fact

Leishmaniasis was first described in 1824, in the Jessore district of Bengal (now Bangladesh) and more prevalent in Bihar, Uttar Pradesh, Jharkhand, and West Bengal. The disease is associated with depressed cellular immunity. Tinea is a fungal infection of the skin, which can become more extensively...

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Main Authors: Amresh Kumar Singh, Ankur Kumar, Jayesh Pandey, Vivek Gaur, Pratima Tripathi, Indra Prasad Adhikari
Format: Article
Language:English
Published: Wiley 2021-01-01
Series:Case Reports in Dermatological Medicine
Online Access:http://dx.doi.org/10.1155/2021/5526435
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author Amresh Kumar Singh
Ankur Kumar
Jayesh Pandey
Vivek Gaur
Pratima Tripathi
Indra Prasad Adhikari
author_facet Amresh Kumar Singh
Ankur Kumar
Jayesh Pandey
Vivek Gaur
Pratima Tripathi
Indra Prasad Adhikari
author_sort Amresh Kumar Singh
collection DOAJ
description Leishmaniasis was first described in 1824, in the Jessore district of Bengal (now Bangladesh) and more prevalent in Bihar, Uttar Pradesh, Jharkhand, and West Bengal. The disease is associated with depressed cellular immunity. Tinea is a fungal infection of the skin, which can become more extensively pathogenic particularly in patients with depressed cell-mediated immunity. Regulatory T cells and Th17 cells have been shown to be responsible for post-kala-azar dermal leishmaniasis (PKDL). We present a rare case of a 52-year-old house wife with a history of recurrent itching, depigmentation of the skin of extremities, and loss of appetite for 2-3 months followed by progressive spread of such lesion all over the body in an apparently healthy female. On examination, there were many hypopigmented scaly lesions mainly over the extensor aspect of the body. Skin lesions were characteristics of tinea infection with or without PKDL. A diagnosis of PKDL with tinea was made based on the history of kala-azar and on the skin slit smear for amastigote forms, rK39 test, and KOH mount. Routine blood investigations showed negative serology for HIV and lower normal CD4+T counts. The patient was advised for treatment on systemic antifungal therapy with antihistaminics and later with miltefosine. We have highlighted that PKDL, although uncommon, is a distinct manifestation of VL. In our case study, we also tried to find the reason of coinfection; this was probably due to the depressed cellular immunity, skin abruptions, and acquired dermatophytic infection which is prevalent and associated with lower CD4+ T cell count.
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spelling doaj-art-c8743582d9db4cd382579db783d7e6d32025-02-03T01:21:34ZengWileyCase Reports in Dermatological Medicine2090-64632090-64712021-01-01202110.1155/2021/55264355526435Mixed Cutaneous Infection Caused by Leishmania and Dermatophytes: A Rare Coincidence or Immunological FactAmresh Kumar Singh0Ankur Kumar1Jayesh Pandey2Vivek Gaur3Pratima Tripathi4Indra Prasad Adhikari5Department of Microbiology, Baba Raghav Das Medical College, Gorakhpur, Uttar Pradesh 273013, IndiaDepartment of Microbiology, Baba Raghav Das Medical College, Gorakhpur, Uttar Pradesh 273013, IndiaDepartment of Microbiology, Baba Raghav Das Medical College, Gorakhpur, Uttar Pradesh 273013, IndiaDepartment of Microbiology, Baba Raghav Das Medical College, Gorakhpur, Uttar Pradesh 273013, IndiaDepartment of Microbiology, Baba Raghav Das Medical College, Gorakhpur, Uttar Pradesh 273013, IndiaDepartment of Biochemistry, Baba Raghav Das Medical College, Gorakhpur, Uttar Pradesh 273013, IndiaLeishmaniasis was first described in 1824, in the Jessore district of Bengal (now Bangladesh) and more prevalent in Bihar, Uttar Pradesh, Jharkhand, and West Bengal. The disease is associated with depressed cellular immunity. Tinea is a fungal infection of the skin, which can become more extensively pathogenic particularly in patients with depressed cell-mediated immunity. Regulatory T cells and Th17 cells have been shown to be responsible for post-kala-azar dermal leishmaniasis (PKDL). We present a rare case of a 52-year-old house wife with a history of recurrent itching, depigmentation of the skin of extremities, and loss of appetite for 2-3 months followed by progressive spread of such lesion all over the body in an apparently healthy female. On examination, there were many hypopigmented scaly lesions mainly over the extensor aspect of the body. Skin lesions were characteristics of tinea infection with or without PKDL. A diagnosis of PKDL with tinea was made based on the history of kala-azar and on the skin slit smear for amastigote forms, rK39 test, and KOH mount. Routine blood investigations showed negative serology for HIV and lower normal CD4+T counts. The patient was advised for treatment on systemic antifungal therapy with antihistaminics and later with miltefosine. We have highlighted that PKDL, although uncommon, is a distinct manifestation of VL. In our case study, we also tried to find the reason of coinfection; this was probably due to the depressed cellular immunity, skin abruptions, and acquired dermatophytic infection which is prevalent and associated with lower CD4+ T cell count.http://dx.doi.org/10.1155/2021/5526435
spellingShingle Amresh Kumar Singh
Ankur Kumar
Jayesh Pandey
Vivek Gaur
Pratima Tripathi
Indra Prasad Adhikari
Mixed Cutaneous Infection Caused by Leishmania and Dermatophytes: A Rare Coincidence or Immunological Fact
Case Reports in Dermatological Medicine
title Mixed Cutaneous Infection Caused by Leishmania and Dermatophytes: A Rare Coincidence or Immunological Fact
title_full Mixed Cutaneous Infection Caused by Leishmania and Dermatophytes: A Rare Coincidence or Immunological Fact
title_fullStr Mixed Cutaneous Infection Caused by Leishmania and Dermatophytes: A Rare Coincidence or Immunological Fact
title_full_unstemmed Mixed Cutaneous Infection Caused by Leishmania and Dermatophytes: A Rare Coincidence or Immunological Fact
title_short Mixed Cutaneous Infection Caused by Leishmania and Dermatophytes: A Rare Coincidence or Immunological Fact
title_sort mixed cutaneous infection caused by leishmania and dermatophytes a rare coincidence or immunological fact
url http://dx.doi.org/10.1155/2021/5526435
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