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[播散性旧世界利什曼病:首例免疫功能正常成人的摩洛哥病例?]

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

作者信息

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

机构信息

Service de dermatologie-vénérologie, Centre hospitalier Ibn Rochd, Casablanca, Maroc.

Laboratoire de pathologie cellulaire et moléculaire, Equipe: immunopathologie des maladies infectieuses et de système, Faculté de médecine et de pharmacie, Université Hassan II de Casablanca, Maroc.

出版信息

Med Trop Sante Int. 2021 Nov 5;1(4). doi: 10.48327/mtsi.2021.90. eCollection 2021 Dec 31.

Abstract

BACKGROUND

Post-kala-azar dermal (PKDL) is a rare skin syndrome observed after treatment of visceral (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 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 bodies. ITS1 PCR was positive (genus 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.

摘要

背景

黑热病后皮肤利什曼病(PKDL)是在用五价有机锑盐治疗内脏利什曼病(VL)后观察到的一种罕见皮肤综合征,此前在摩洛哥从未有过描述。在此,我们报告一例免疫功能正常的成年人病例。

病例

一名来自摩洛哥南部塔塔的36岁男性,有2年前患内脏利什曼病的病史,曾用葡甲胺锑酸盐和两性霉素B治疗,临床过程良好,因面部出现红斑丘疹结节性皮疹而入住皮肤科。6个月前,他出现口腔黏膜受累,3个月后,面部出现皮肤病变。皮肤科检查发现丘疹结节性红斑皮疹延伸至鼻子和双颊,前额、眼周和下巴有结痂和狼疮样病变,足跟有溃疡性无痛病变。口腔黏膜检查发现舌后三分之一处溃疡,软腭呈乳头状。皮肤活检和涂片发现一些无鞭毛体形式的虫体。内转录间隔区1(ITS1)聚合酶链反应(PCR)呈阳性(利什曼原虫属)。艾滋病毒血清学检查为阴性。随后诊断为PKDL。患者接受了葡甲胺锑酸盐肌肉注射,病情进展良好。

结论

据我们所知,这是摩洛哥首例报告的提示PKDL的免疫功能正常成年人的全身性利什曼病病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee8b/9283810/9485cf79279c/mtsi-01-5246-g001.jpg

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