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汗疱疹样大疱性类天疱疮。

Dyshidrosiform Bullous Pemphigoid.

机构信息

San Diego Family Dermatology, National City, CA 91950, USA.

College of Osteopathic Medicine, Touro University California, Vallejo, CA 94589, USA.

出版信息

Medicina (Kaunas). 2021 Apr 20;57(4):398. doi: 10.3390/medicina57040398.

DOI:10.3390/medicina57040398
PMID:33924249
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8074754/
Abstract

Dyshidrosiform bullous pemphigoid is a variant of bullous pemphigoid. At least 84 patients with dyshidrosiform bullous pemphigoid have been described. Dyshidrosiform bullous pemphigoid usually presents with pruritic blisters in elderly individuals; the hemorrhagic or purpuric lesions on the palms and soles can be the only manifestation of the disease. However, bullae may concurrently or subsequently appear on other areas of the patient's body. Patients typically improve after the diagnosis is established and treatment is initiated. The mainstay of therapy is systemic corticosteroids, with or without topical corticosteroids, and systemic dapsone or immunosuppressants. Drug-related or nickel-induced dyshidrosiform bullous pemphigoid improves after stopping the associated agent; however, systemic therapy has also been required to achieve resolution of the blisters. Similar to classic bullous pemphigoid, neurologic conditions and psychiatric disorders have been observed in dyshidrosiform bullous pemphigoid patients. The new onset of recurrent or persistent blisters on the palms, soles, or both of an elderly individual should prompt the clinician to consider the diagnosis of dyshidrosiform bullous pemphigoid.

摘要

汗疱疹样大疱性类天疱疮是大疱性类天疱疮的一种变体。至少已经描述了 84 例汗疱疹样大疱性类天疱疮患者。汗疱疹样大疱性类天疱疮通常发生于老年人,表现为瘙痒性水疱;手掌和足底的出血性或紫癜性损害可能是该病的唯一表现。然而,水疱可能同时或随后出现在患者身体的其他部位。在确诊并开始治疗后,患者通常会有所改善。治疗的主要方法是全身性皮质类固醇,联合或不联合局部皮质类固醇,以及全身性氨苯砜或免疫抑制剂。与药物或镍相关的汗疱疹样大疱性类天疱疮在停用相关药物后会改善;然而,也需要全身治疗才能使水疱消退。与经典大疱性类天疱疮类似,汗疱疹样大疱性类天疱疮患者也观察到神经状况和精神障碍。老年人手掌、足底或两者同时出现新发复发性或持续性水疱时,临床医生应考虑汗疱疹样大疱性类天疱疮的诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57d6/8074754/093c07890860/medicina-57-00398-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57d6/8074754/5434e30beec5/medicina-57-00398-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57d6/8074754/1c9c542ac487/medicina-57-00398-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57d6/8074754/d9e1e50c7e3f/medicina-57-00398-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57d6/8074754/093c07890860/medicina-57-00398-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57d6/8074754/5434e30beec5/medicina-57-00398-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57d6/8074754/1c9c542ac487/medicina-57-00398-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57d6/8074754/d9e1e50c7e3f/medicina-57-00398-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57d6/8074754/093c07890860/medicina-57-00398-g004.jpg

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本文引用的文献

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J Eur Acad Dermatol Venereol. 2021 Apr;35(4):973-980. doi: 10.1111/jdv.16996. Epub 2020 Nov 17.
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Bullous Pemphigoid: Trigger and Predisposing Factors.大疱性类天疱疮:触发因素和易感因素。
Biomolecules. 2020 Oct 10;10(10):1432. doi: 10.3390/biom10101432.
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A Systematic Review of Drug-Induced Pemphigoid.药物性类天疱疮的系统评价
汗疱疹样大疱性类天疱疮的诊断挑战:一个手掌难题。
Cureus. 2024 Aug 8;16(8):e66470. doi: 10.7759/cureus.66470. eCollection 2024 Aug.
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Involvement of palms and soles in patients with autoimmune bullous diseases: a comparative analysis of a diagnostically relevant localization.手掌和足底在自身免疫性大疱性疾病患者中的累及:一种具有诊断相关性的定位的比较分析。
Front Immunol. 2023 Oct 10;14:1227855. doi: 10.3389/fimmu.2023.1227855. eCollection 2023.
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Intravenous immunoglobulins in infantile dyshidrosiform bullous pemphigoid refractory to steroids and dapsone.静脉注射免疫球蛋白治疗对类固醇和氨苯砜难治的婴儿汗疱状大疱性类天疱疮
Dermatol Ther. 2022 Nov;35(11):e15826. doi: 10.1111/dth.15826. Epub 2022 Sep 27.
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Hemidesmosomal Reactivity and Treatment Recommendations in Immune Checkpoint Inhibitor-Induced Bullous Pemphigoid-A Retrospective, Monocentric Study.免疫检查点抑制剂诱导性大疱性类天疱疮的半桥粒反应和治疗建议:一项回顾性单中心研究。
Front Immunol. 2022 Jul 22;13:953546. doi: 10.3389/fimmu.2022.953546. eCollection 2022.
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