Mapesi Herry, Ramírez Adrià, Tanner Marcel, Hatz Christoph, Letang Emilio
Chronic Diseases Clinic of Ifakara, Ifakara Health Institute, P. O Box 53, Ifakara, Tanzania.
University of Basel, Basel, Switzerland.
BMC Infect Dis. 2016 Sep 20;16:495. doi: 10.1186/s12879-016-1824-4.
Immune reconstitution inflammatory syndrome associated with dermatophytoses (tinea-IRIS) may cause considerable morbidity. Yet, it has been scarcely reported and is rarely considered in the differential diagnosis of HIV associated cutaneous lesions in Africa. If identified, it responds well to antifungals combined with steroids. We present two cases of suspected tinea-immune reconstitution inflammatory syndrome from a large HIV clinic in rural Tanzania.
A first case was a 33 years-old female newly diagnosed HIV patient with CD4 count of 4 cells/μL (0 %), normal complete blood count, liver and renal function tests was started on co-formulated tenofovir/emtricitabine/efavirenz and prophylactic cotrimoxazole. Two weeks later she presented with exaggerated inflammatory hyperpigmented skin plaques with central desquamation, active borders and scratch lesions on the face, trunk and lower limbs. Tinea-IRIS was suspected and fluconazole (150 mg daily) and prednisolone (1 mg/Kg/day tapered down after 1 week) were given. Her symptoms subsided completely after 8 weeks of treatment, and her next CD4 counts had increased to 134 cells/μL (11 %). The second case was a 35 years-old female newly diagnosed with HIV. She had 1 CD4 cell/μL (0 %), haemoglobin 9.8 g/dl, and normal renal and liver function tests. Esophageal candidiasis and normocytic-normochromic anaemia were diagnosed. She received fluconazole, prophylactic cotrimoxazole and tenofovir/emtricitabine/efavirenz. Seven weeks later she presented with inflammatory skin plaques with elevated margins and central hyperpigmentation on the trunk, face and limbs in the frame of a good general recovery and increased CD4 counts (188 cells/μL, 6 %). Tinea-IRIS was suspected and treated with griseofulvin 500 mg daily and prednisolone 1 mg/Kg tapered down after 1 week, with total resolution of symptoms in 2 weeks.
The two cases had advanced immunosuppression and developed de-novo exaggerated manifestation of inflammatory lesions compatible with tinea corporis and tinea facies in temporal association with antiretroviral treatment initiation and good immunological response. This is compatible with unmasking tinea-IRIS, and reminds African clinicians about the importance of considering this entity in the differential diagnosis of patients with skin lesions developing after antiretroviral treatment initiation.
与皮肤癣菌病相关的免疫重建炎症综合征(癣菌性免疫重建炎症综合征,tinea - IRIS)可能导致相当高的发病率。然而,在非洲,关于它的报道很少,在HIV相关皮肤病变的鉴别诊断中也很少被考虑。如果确诊,其对抗真菌药物联合类固醇治疗反应良好。我们报告了来自坦桑尼亚农村一家大型HIV诊所的两例疑似癣菌性免疫重建炎症综合征病例。
第一例是一名33岁新诊断的HIV女性患者,CD4细胞计数为4个/μL(0%),全血细胞计数、肝肾功能检查正常,开始服用复方替诺福韦/恩曲他滨/依非韦伦及预防性复方新诺明。两周后,她出现了炎症性色素沉着过度的皮肤斑块,中央有脱屑,边界活跃,面部、躯干和下肢有抓痕性皮损。怀疑为癣菌性免疫重建炎症综合征,给予氟康唑(每日150mg)和泼尼松龙(1mg/kg/天,1周后逐渐减量)。治疗8周后症状完全消退,其下次CD4细胞计数升至134个/μL(11%)。第二例是一名新诊断为HIV的35岁女性。她的CD4细胞计数为1个/μL(0%),血红蛋白9.8g/dl,肝肾功能检查正常。诊断为食管念珠菌病和正细胞正色素性贫血。她接受了氟康唑、预防性复方新诺明和替诺福韦/恩曲他滨/依非韦伦治疗。7周后,在全身状况良好且CD4细胞计数增加(188个/μL,6%)的情况下,她在躯干、面部和四肢出现了边缘隆起和中央色素沉着的炎症性皮肤斑块。怀疑为癣菌性免疫重建炎症综合征,给予灰黄霉素每日500mg和泼尼松龙1mg/kg,1周后逐渐减量,2周内症状完全消退。
这两例患者均有严重免疫抑制,在开始抗逆转录病毒治疗并出现良好免疫反应的同时,出现了与体癣和面部癣相符的新发炎症性病变的过度表现。这与揭示癣菌性免疫重建炎症综合征相符,并提醒非洲临床医生在鉴别诊断抗逆转录病毒治疗开始后出现皮肤病变的患者时考虑这一疾病的重要性。