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An Unusual TEN-Like Presentation of Juvenile Bullous Pemphigoid: A Diagnostic Challenge.

作者信息

Nikyar Zahra, Hatami Parvaneh, Aryanian Zeinab, Sotoudeh Soheila, Ziaee Vahid, Goodarzi Azadeh

机构信息

Autoimmune Bullous Diseases Research Center, Tehran University of Medical Sciences, Tehran, Iran.

Department of Dermatology, Skin Diseases and Leishmaniasis Research Center, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.

出版信息

Case Rep Dermatol Med. 2022 Apr 11;2022:8507156. doi: 10.1155/2022/8507156. eCollection 2022.

DOI:10.1155/2022/8507156
PMID:35449587
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9017583/
Abstract

Bullous pemphigoid (BP) is an acquired autoimmune bullous disorder rarely seen in the pediatric population. It usually presents as large and tense bullae, predominantly distributed in the acral areas. Herein, we describe a case of childhood BP with an atypical presentation mimicking toxic epidermal necrolysis (TEN). This case shows us that juvenile BP should be considered in the differential diagnosis of TEN in children, particularly if there are unusual features and an intractable course.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac4c/9017583/5ae9a802aea0/CRIDM2022-8507156.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac4c/9017583/e32d1b5e9dc9/CRIDM2022-8507156.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac4c/9017583/d4b5b76d1f6c/CRIDM2022-8507156.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac4c/9017583/5ae9a802aea0/CRIDM2022-8507156.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac4c/9017583/e32d1b5e9dc9/CRIDM2022-8507156.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac4c/9017583/d4b5b76d1f6c/CRIDM2022-8507156.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac4c/9017583/5ae9a802aea0/CRIDM2022-8507156.003.jpg

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Front Immunol. 2022 Jan 24;13:824110. doi: 10.3389/fimmu.2022.824110. eCollection 2022.
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Risk Factors for Mucosal Involvement in Bullous Pemphigoid and the Possible Mechanism: A Review.大疱性类天疱疮黏膜受累的危险因素及可能机制：综述
Front Med (Lausanne). 2021 May 20;8:680871. doi: 10.3389/fmed.2021.680871. eCollection 2021.
3
Bullous pemphigoid secondary to pembrolizumab mimicking toxic epidermal necrolysis.
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JAAD Case Rep. 2020 Apr 29;6(5):400-402. doi: 10.1016/j.jdcr.2020.03.003. eCollection 2020 May.
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Severe Infantile Bullous Pemphigoid Treated with Dapsone after Bridging with Systemic Glucocorticoid.在使用全身性糖皮质激素进行过渡后，用氨苯砜治疗重症婴儿大疱性类天疱疮。
Case Rep Dermatol. 2019 Jun 26;11(2):187-193. doi: 10.1159/000501359. eCollection 2019 May-Aug.
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