De La Hoz Alejandro, Gadi Nirupa, Lopez Christina G, Barrera-Godinez Alejandro, Miller Nancy S, Bourque Daniel L, Brem Candice, Ozluk Ekin, Seth Geetika, Kimball Sarah, Taylor Jessica L
Department of Medicine, Boston Medical Center, Boston University Chobanian and Avedisian School of Medicine, Boston, Massachusetts, USA.
Department of Dermatology, Boston Medical Center, Boston University Chobanian and Avedisian School of Medicine, Boston, Massachusetts, USA.
Open Forum Infect Dis. 2024 Oct 14;11(10):ofae587. doi: 10.1093/ofid/ofae587. eCollection 2024 Oct.
Migration routes determine exposure to endemic infections. We present a case of complex cutaneous leishmaniasis in a man with HIV infection who migrated to the United States from Haiti, where is uncommon, acquiring leishmaniasis while on his journey via South America and Central America. His presentation included hyperpigmented, nonulcerated plaques and nodules on his extremities, chest, back, face, palms, and soles; initially he had no mucosal lesions. Infection with was confirmed via polymerase chain reaction. He was prescribed bictegravir/tenofovir alafenamide/emtricitabine with rapid suppression of HIV and liposomal amphotericin B for diffuse cutaneous leishmaniasis with a limited initial response. He subsequently developed mucosal lesions in the setting of immune reconstitution and was retreated with amphotericin dosed for mucocutaneous disease. A thorough migration history was critical to diagnosis. This case highlights the different presentations of leishmaniasis in people with HIV and the elevated risk for treatment failure.
迁移路线决定了地方性感染的暴露情况。我们报告一例复杂皮肤利什曼病病例,患者为一名感染艾滋病毒的男性,他从海地移民到美国,海地利什曼病并不常见,他在经由南美洲和中美洲的旅程中感染了利什曼病。他的症状包括四肢、胸部、背部、面部、手掌和脚底出现色素沉着、无溃疡的斑块和结节;最初他没有黏膜病变。通过聚合酶链反应确诊感染利什曼原虫。他被开了比克替拉韦/替诺福韦艾拉酚胺/恩曲他滨,艾滋病毒得到快速抑制,同时还使用了脂质体两性霉素B治疗弥漫性皮肤利什曼病,但初始反应有限。随后,他在免疫重建过程中出现了黏膜病变,并再次接受针对黏膜皮肤疾病剂量的两性霉素治疗。详尽的迁移史对诊断至关重要。该病例突出了艾滋病毒感染者中利什曼病的不同表现以及治疗失败风险的升高。