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获得性反应性穿通性胶原病合并耐甲氧西林金黄色葡萄球菌感染:一例报告。

Acquired reactive perforating collagenosis combined with MRSA: A case report.

作者信息

Huang Fuqian, Ren Weiqi, Wang Miaomiao, Li Xiufang, Pan Min

机构信息

Department of Dermatology, Affiliated Hospital of Qingdao University, Qingdao, Shandong 266003, P.R. China.

出版信息

Med Int (Lond). 2023 Jan 26;3(1):9. doi: 10.3892/mi.2023.69. eCollection 2023 Jan-Feb.

Abstract

Acquired reactive perforating collagenosis (ARPC) is a rare chronic skin disease associated with various internal diseases, particularly diabetes and chronic renal failure. The present study describes the case of a patient with ARPC combined with methicillin-resistant (MRSA), in an aim to broaden the current understanding of ARPC. A 75-year-old female presented with a 5-year history of pruritus and ulcerative eruptions on the trunk of her body, which became more severe within 1 year. A cutaneous examination revealed a diffuse distribution of erythema and papules, and nodules of various sizes, some of which sagged at the center and had a dark brown crust. A histopathological analysis revealed typical perforations of the collagen fibers. The patient was initially treated with topical corticosteroids and oral antihistamines for skin lesions and pruritus. Medications for glucose control were also administered. Upon the second admission, a combination of antibiotics and acitretin was added. The keratin plug shrank, and the pruritus was relieved. To date, to the best of our knowledge, this is the first reported case of concurrent ARPC and MRSA.

摘要

获得性反应性穿通性胶原病(ARPC)是一种罕见的慢性皮肤病,与多种内科疾病相关,尤其是糖尿病和慢性肾衰竭。本研究描述了一例合并耐甲氧西林金黄色葡萄球菌(MRSA)感染的ARPC患者,旨在拓宽当前对ARPC的认识。一名75岁女性,躯干出现瘙痒和溃疡性皮疹5年,近1年内病情加重。皮肤检查发现红斑、丘疹弥漫分布,还有大小不一的结节,部分结节中央凹陷,有深褐色痂皮。组织病理学分析显示胶原纤维有典型的穿通现象。患者最初接受局部糖皮质激素和口服抗组胺药治疗皮肤损害及瘙痒。同时给予控制血糖的药物。第二次入院时,加用了抗生素和阿维A。角质栓缩小,瘙痒缓解。据我们所知,这是首例并发ARPC和MRSA的报道病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f49/9922796/9adb45256f87/mi-03-01-00069-g00.jpg

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