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Leishmaniose généralisée de l'Ancien monde : Premier cas marocain chez un adulte immunocompétent ?
BACKGROUND: Post-kala-azar dermal Leishmaniasis (PKDL) is a rare skin syndrome observed after treatment of visceral Leishmaniasis (VL) with pentavalent antimonial organic salts, never described in Morocco before. Here we report a case in an immunocompetent adult. CASE: A 36-year-old-man from Tata in...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MTSI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9283810/ https://www.ncbi.nlm.nih.gov/pubmed/35891918 http://dx.doi.org/10.48327/mtsi.2021.90 |
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author | CHIHEB, Soumiya TAZI SAOUD, Zineb EL IDRISSI SAIK, Imane DARIF, Dounia HALI, Fouzia FATOIKI, Fatima Zahra El DAHBI, Hayat Skali KIHEL, Ayyoub HAMMI, Ikram SOUSSI ABDELLAOUI, Maha RIYAD, Myriam |
author_facet | CHIHEB, Soumiya TAZI SAOUD, Zineb EL IDRISSI SAIK, Imane DARIF, Dounia HALI, Fouzia FATOIKI, Fatima Zahra El DAHBI, Hayat Skali KIHEL, Ayyoub HAMMI, Ikram SOUSSI ABDELLAOUI, Maha RIYAD, Myriam |
author_sort | CHIHEB, Soumiya |
collection | PubMed |
description | BACKGROUND: Post-kala-azar dermal Leishmaniasis (PKDL) is a rare skin syndrome observed after treatment of visceral Leishmaniasis (VL) with pentavalent antimonial organic salts, never described in Morocco before. Here we report a case in an immunocompetent adult. CASE: A 36-year-old-man from Tata in southern Morocco, with a history of visceral Leishmaniasis 2 years before and treated with meglumine antimoniate and amphotericin B with good clinical course, was hospitalized in dermatology for an erythematous papulo-nodular closet of the face. Six months ago, he presented oral mucosa involvement, then 3 months later, cutaneous lesions appeared on the face. The dermatological examination revealed a papulo-nodular erythematous closet extending to the nose and both cheeks, crusty and lupoid lesions on the forehead, around the eyes and chin, associated with an ulcerative and painless lesion on the heeL. The examination of the oral mucosa revealed an ulceration of the posterior third of the tongue and a papillomatous aspect of the soft palate. The skin biopsy and smear found some amastigote forms of Leishmania bodies. ITS1 PCR was positive (genus Leishmania). The HIV serology was negative. The diagnosis of PKDL was then evoked. The patient received intra-muscular injections of meglumine antimoniate with good progress. CONCLUSION: To our knowledge, this is the first case of generalised leishmaniasis suggesting PKDL reported in a Moroccan immunocompetent adult. |
format | Online Article Text |
id | pubmed-9283810 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MTSI |
record_format | MEDLINE/PubMed |
spelling | pubmed-92838102022-07-25 Leishmaniose généralisée de l'Ancien monde : Premier cas marocain chez un adulte immunocompétent ? CHIHEB, Soumiya TAZI SAOUD, Zineb EL IDRISSI SAIK, Imane DARIF, Dounia HALI, Fouzia FATOIKI, Fatima Zahra El DAHBI, Hayat Skali KIHEL, Ayyoub HAMMI, Ikram SOUSSI ABDELLAOUI, Maha RIYAD, Myriam Med Trop Sante Int Microbiologie BACKGROUND: Post-kala-azar dermal Leishmaniasis (PKDL) is a rare skin syndrome observed after treatment of visceral Leishmaniasis (VL) with pentavalent antimonial organic salts, never described in Morocco before. Here we report a case in an immunocompetent adult. CASE: A 36-year-old-man from Tata in southern Morocco, with a history of visceral Leishmaniasis 2 years before and treated with meglumine antimoniate and amphotericin B with good clinical course, was hospitalized in dermatology for an erythematous papulo-nodular closet of the face. Six months ago, he presented oral mucosa involvement, then 3 months later, cutaneous lesions appeared on the face. The dermatological examination revealed a papulo-nodular erythematous closet extending to the nose and both cheeks, crusty and lupoid lesions on the forehead, around the eyes and chin, associated with an ulcerative and painless lesion on the heeL. The examination of the oral mucosa revealed an ulceration of the posterior third of the tongue and a papillomatous aspect of the soft palate. The skin biopsy and smear found some amastigote forms of Leishmania bodies. ITS1 PCR was positive (genus Leishmania). The HIV serology was negative. The diagnosis of PKDL was then evoked. The patient received intra-muscular injections of meglumine antimoniate with good progress. CONCLUSION: To our knowledge, this is the first case of generalised leishmaniasis suggesting PKDL reported in a Moroccan immunocompetent adult. MTSI 2021-11-05 /pmc/articles/PMC9283810/ /pubmed/35891918 http://dx.doi.org/10.48327/mtsi.2021.90 Text en Copyright © 2021 SFMTSI https://creativecommons.org/licenses/by/4.0/Cet article en libre accès est distribué selon les termes de la licence Creative Commons CC BY 4.0 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Microbiologie CHIHEB, Soumiya TAZI SAOUD, Zineb EL IDRISSI SAIK, Imane DARIF, Dounia HALI, Fouzia FATOIKI, Fatima Zahra El DAHBI, Hayat Skali KIHEL, Ayyoub HAMMI, Ikram SOUSSI ABDELLAOUI, Maha RIYAD, Myriam Leishmaniose généralisée de l'Ancien monde : Premier cas marocain chez un adulte immunocompétent ? |
title | Leishmaniose généralisée de l'Ancien monde : Premier cas marocain chez un adulte immunocompétent ? |
title_full | Leishmaniose généralisée de l'Ancien monde : Premier cas marocain chez un adulte immunocompétent ? |
title_fullStr | Leishmaniose généralisée de l'Ancien monde : Premier cas marocain chez un adulte immunocompétent ? |
title_full_unstemmed | Leishmaniose généralisée de l'Ancien monde : Premier cas marocain chez un adulte immunocompétent ? |
title_short | Leishmaniose généralisée de l'Ancien monde : Premier cas marocain chez un adulte immunocompétent ? |
title_sort | leishmaniose généralisée de l'ancien monde : premier cas marocain chez un adulte immunocompétent ? |
topic | Microbiologie |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9283810/ https://www.ncbi.nlm.nih.gov/pubmed/35891918 http://dx.doi.org/10.48327/mtsi.2021.90 |
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