[Generalized old world leishmaniasis: first Moroccan case in an immunocompetent adult?]

Medecine tropicale et sante internationale Pub Date : 2021-11-05 eCollection Date: 2021-12-31 DOI:10.48327/mtsi.2021.90
Soumiya Chiheb, Zineb Tazi Saoud, Imane El Idrissi Saik, Dounia Darif, Fouzia Hali, Fatima Zahra El Fatoiki, Hayat Skali Dahbi, Ayyoub Kihel, Ikram Hammi, Maha Soussi Abdellaoui, Myriam Riyad
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Abstract

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.

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广泛性旧大陆利什曼病:摩洛哥首例免疫功能正常的成人病例?]
背景:黑热病后皮肤利什曼病(PKDL)是用五价锑有机盐治疗内脏利什曼病(VL)后观察到的一种罕见的皮肤综合征,在摩洛哥以前从未报道过。在此,我们报告一例免疫功能正常的成年人。病例:一名来自摩洛哥南部塔塔的36岁男子,2年前有内脏利什曼病病史,曾接受锑酸甲氨胺和两性霉素B治疗,临床病程良好,因面部丘疹结节性红斑而住院。6个月前出现口腔黏膜受累,3个月后出现面部皮肤病变。皮肤病学检查发现丘疹结节性红斑,延伸至鼻子和双颊,前额、眼睛周围和下巴有硬壳样和脂样病变,脚跟处有溃疡性无痛病变。口腔黏膜检查显示舌头后三分之一处有溃疡,软腭有乳头状瘤。皮肤活检和涂片发现一些利什曼原虫体的无鞭毛体。ITS1 PCR阳性(利什曼属)。HIV血清学结果为阴性。诱发PKDL的诊断。患者接受肌内注射甲氨苄胺,进展良好。结论:据我们所知,这是第一例广泛性利什曼病,表明在摩洛哥免疫功能正常的成年人中报告了PKDL。
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