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临床未怀疑的特发性CD4淋巴细胞减少症中的孤立性皮肤隐球菌病。

Isolated cutaneous cryptococcosis in clinically unsuspected idiopathic CD4 lymphocytopenia.

作者信息

Sharma Divya, Singh Neha, Kaushal Seema, Jain Shyama

机构信息

Department of Pathology, Maulana Azad Medical College and Associated LNJP Hospital, New Delhi, India.

出版信息

J Cytol. 2014 Oct-Dec;31(4):230-2. doi: 10.4103/0970-9371.151143.

Abstract

Idiopathic CD4 lymphocytopenia first defined in 1992 by the U.S. Centers for Disease Control and Prevention, as the repeated presence of a CD4(+) T-lymphocyte count of fewer than 300 cells/cumm or of <20% of total T-cells with no evidence of human immunodeficiency virus (HIV) infection and therapy that might cause depressed CD4 T-cells. Most of the cases present with systemic opportunistic infections. We report a case without risk factors or laboratory evidence of HIV infection, presenting with cutaneous cryptococcal infection, diagnosed on cytology.

摘要

特发性CD4淋巴细胞减少症于1992年由美国疾病控制与预防中心首次定义,即CD4(+) T淋巴细胞计数反复低于300个细胞/立方毫米或占总T细胞的比例不足20%,且无人类免疫缺陷病毒(HIV)感染及可能导致CD4 T细胞减少的治疗证据。大多数病例会出现全身性机会性感染。我们报告一例无HIV感染风险因素或实验室证据的病例,该病例表现为皮肤隐球菌感染,经细胞学检查确诊。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fff2/4349021/9c5da6c09b69/JCytol-31-230-g001.jpg

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