新发大疱性类天疱疮1例。

Q3 Medicine Case Reports in Dermatological Medicine Pub Date : 2021-06-07 eCollection Date: 2021-01-01 DOI:10.1155/2021/5575111
Natalie Olson, David Eckhardt, Angela Delano
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引用次数: 20

摘要

本文首次报道了与COVID-19相关的大疱性类天疱疮皮疹。本文的目的是在covid -19阳性感染的背景下提出一个独特的皮肤病学病例,以进一步认识病毒症状。一名37岁女性,既往有III类肥胖、II型糖尿病和高血压病史,于2020年9月到急诊科就诊,住院和门诊随访至2020年11月。患者否认有任何个人或家族皮肤病史。患者入院前COVID-19检测呈阳性,入院时出现严重、持续、瘙痒性皮疹,符合大疱性类天疱疮的皮肤病理学、血清学和临床诊断标准。左屈腕的组织病理学H&E穿刺活检显示表皮角质细胞坏死,表皮下嗜酸性粒细胞囊泡,乳头状真皮如游丝状搁浅,以及表皮下水肿。左屈腕关节的直接免疫荧光穿刺活检显示在真皮表皮连接处有很强的线性IgG染色,有较弱的局灶性线性C3染色。抗原特异性血清学与大疱性类天疱疮一致。之前没有报道过COVID-19感染与大疱性类天疱疮的皮肤关联,这使得该病例成为有助于在病毒感染的情况下识别大疱性类天疱疮的重要证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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New-Onset Bullous Pemphigoid in a COVID-19 Patient.

This manuscript presents a report of bullous pemphigoid rash associated with COVID-19 for the first time. The objective of this manuscript is to present a unique dermatological case in the setting of a COVID-19-positive infection to further recognize the virus symptomatology. A 37-year-old female with a past medical history of class III obesity, type II diabetes mellitus, and hypertension presented to the emergency department in September 2020 with inpatient and outpatient follow-up through to November 2020. The patient denied any personal or family history of skin disorders. The patient tested positive for COVID-19 prior to hospitalization and presented to the hospital with severe, persistent, pruritic rash meeting dermatopathological, serologic, and clinical criteria for bullous pemphigoid diagnosis. Histopathology H&E punch biopsy from her left flexor wrist demonstrated epidermal keratinocyte necrosis, subepidermal vesiculation with eosinophils, gossamer stranding of the papillary dermis, and subepidermal edema. Direct immunofluorescence punch biopsy from her left flexor wrist demonstrated strong linear IgG staining at the dermoepidermal junction, with weaker and focal linear C3 staining. Antigen-specific serology was consistent with bullous pemphigoid. There was no previously reported cutaneous association of COVID-19 infection with bullous pemphigoid making this case an important addition to the body of evidence helping to identify bullous pemphigoid in the setting of viral infection.

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CiteScore
1.50
自引率
0.00%
发文量
24
审稿时长
15 weeks
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