一例罕见病例和文献综述:在硬皮病背景下出现的大疱性类天疱疮:皮肤病理学难题和预期结果。

IF 0.6 Q4 DERMATOLOGY Acta Dermatovenerologica Alpina Pannonica et Adriatica Pub Date : 2024-11-04
Tijana Orlić, Igor Kapetanović, Vesna Reljić, Snežana Minić, Dubravka Živanović
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引用次数: 0

摘要

硬皮病(LS)患者同时出现水疱,会让人产生这样的疑问:这些水疱是 LS 的大疱性变异,还是同时伴有自身免疫性疾病。我们报告了一例罕见的大疱性类天疱疮(BP)病例,该病例发生在 LS 之前的皮损上。据我们所知,这也是文献报道的首例 BP180 阴性病例。在此,我们提出了与 BP 自身抗体无关的其他机制,这些机制可能会导致受 LS 影响的皮肤上出现 BP。此外,我们还提供了一篇文献综述,探讨了潜在的病理生理学,并提供了实用的治疗见解,为临床医生处理类似的复杂病例提供了宝贵的指导。
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A rare case and literature review of bullous pemphigoid appearing in the setting of lichen sclerosus: a dermatopathological conundrum and what to expect.

Co-occurrence of blisters in patients with lichen sclerosus (LS) can raise the question of whether they represent a bullous variant of LS or a concomitant autoimmune disorder. We report a rare case of bullous pemphigoid (BP) occurring on previous LS lesions. To the best of our knowledge, this is also the first BP180-negative case reported in literature. Here, we propose alternative mechanisms, independent of BP autoantibodies, that may lead to development of BP on skin affected by LS. In addition, we provide a literature review that explores the underlying pathophysiology and offers practical treatment insights, equipping clinicians with valuable guidance for similar complex cases.

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来源期刊
CiteScore
1.70
自引率
8.30%
发文量
38
期刊最新文献
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