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©The Author(s) 2025. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Clin Cases. Feb 6, 2025; 13(4): 94294
Published online Feb 6, 2025. doi: 10.12998/wjcc.v13.i4.94294
Published online Feb 6, 2025. doi: 10.12998/wjcc.v13.i4.94294
Bullous pemphigoid associated with acquired hemophilia A: A case report
Su-Ye Hu, Zi-Jia Hao, Xu-Ya Chai, Pei-Sai Li, Yang Liu, Pan-Pan Yang, Ling-E Li, Department of Dermatology, Shijiazhuang Traditional Chinese Medicine Hospital, Shijiazhuang 050051, Hebei Province, China
Meng-Can Li, Graduate School, Hebei University of Traditional Chinese Medicine, Shijiazhuang 050051, Hebei Province, China
Li-Xia Liu, Ying Xu, Department of Pathology, Shijiazhuang Traditional Chinese Medicine Hospital, Shijiazhuang 050051, Hebei Province, China
Co-first authors: Su-Ye Hu and Meng-Can Li.
Co-corresponding authors: Pan-Pan Yang and Ling-E Li.
Author contributions: Chai XY and Hao ZJ performed laboratory testing and clinical data collection; Li PS and Liu Y performed pathological studies; Liu LX and Xu Y approved the pathological studies; Hu SY and Li MC drafted the manuscript; Yang PP and Li LE critically revised the manuscript for important intellectual content. All authors have read and approved the final version.
Supported by Traditional Chinese Medicine Research Program of Hebei Provincial Administration of Traditional Chinese Medicine, No. 2025313 and No. 2025448.
Informed consent statement: Informed written consent was obtained from the patient for the publication of this case report.
Conflict-of-interest statement: The authors declare that they have no conflicts of interest to disclose.
CARE Checklist (2016) statement: The authors have read the CARE Checklist (2016), and the manuscript was prepared and revised according to the CARE Checklist (2016).
Open-Access: This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/
Corresponding author: Ling-E Li, BSc, Chief Physician, Department of Dermatology, Shijiazhuang TCM Hospital, No. 233 Zhongshan West Road, Qiaoxi District, Shijiazhuang 050051, Hebei Province, China. zyypfk2008@126.com
Received: March 21, 2024
Revised: September 29, 2024
Accepted: November 4, 2024
Published online: February 6, 2025
Processing time: 238 Days and 16.7 Hours
Revised: September 29, 2024
Accepted: November 4, 2024
Published online: February 6, 2025
Processing time: 238 Days and 16.7 Hours
Core Tip
Core Tip: Bullous pemphigoid associated with acquired hemophilia A is a rare disorder with unknown etiology and a high mortality rate. Because it develops in patients without a known bleeding disorder, clinicians should be aware of it and ensure its timely diagnosis and appropriate and effective treatment.