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获得性免疫缺陷综合征中的播散性环状肉芽肿:病例报告及文献复习

Disseminated granuloma annulare in acquired immunodeficiency syndrome: case report and review of the literature.

作者信息

Calista D, Landi G

机构信息

Department of Dermatology, Ospedale M. Bufalini, Cesena, Italy.

出版信息

Cutis. 1995 Mar;55(3):158-60.

PMID:7634846
Abstract

The authors report the case of a 27-year-old woman who presented with disseminated granuloma annulare in association with acquired immunodeficiency syndrome. The lesions were asymptomatic, tiny, erythematous or flesh-colored umbilicated papules on the neck, trunk, and flexor surface of the arms and knees that regressed without any treatment in two months. The case reported is the nineteenth description of the association of granuloma annulare and acquired immunodeficiency syndrome but the first in a female patient. The causes and pathogenesis of granuloma annulare are unknown, but after reviewing the previous case reports we hypothesize that circulating human immunodeficiency virus particles may be a precipitating factor in granuloma annulare and that the CD4+ and CD8+ cell dysfunction may be responsible for the atypically short course of the disease.

摘要

作者报告了一例27岁女性患者,该患者患有播散性环状肉芽肿并伴有获得性免疫缺陷综合征。皮损无症状,为颈部、躯干以及手臂和膝盖屈侧的微小、红斑或肤色脐凹状丘疹,在未进行任何治疗的情况下,两个月内自行消退。该病例报告是环状肉芽肿与获得性免疫缺陷综合征关联的第19例描述,但却是首例女性患者。环状肉芽肿的病因和发病机制尚不清楚,但在回顾之前的病例报告后,我们推测循环中的人类免疫缺陷病毒颗粒可能是环状肉芽肿的促发因素,而CD4+和CD8+细胞功能障碍可能是导致该疾病非典型短病程的原因。

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