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妊娠类天疱疮:一例病例报告及文献综述

Pemphigoid gestationis: a case report and review of the literature.

作者信息

Campbell Shannon M, Balazs Kathryn, Conroy Michael

机构信息

Ohio University College of Osteopathic Medicine, O'Bleness Memorial Hospital Dermatology Residency Program, Athens, USA.

出版信息

Cutis. 2011 Jul;88(1):21-6.

Abstract

Pemphigoid gestationis (PG) is an uncommon autoimmune bullous disease that almost exclusively presents during pregnancy. Patients typically present with a diffuse blistering and intensely pruritic eruption that begins periumbilically and spreads to involve the rest of the body. Direct immunofluorescence demonstrating C3 in a linear pattern along the dermoepidermal junction confirms the diagnosis of PG. Corticosteroids remain the choice of therapy and early intervention is essential because of possible adverse effects of PG on the fetus. We report a case of PG and review the literature.

摘要

妊娠类天疱疮(PG)是一种罕见的自身免疫性大疱性疾病,几乎仅在孕期出现。患者通常表现为弥漫性水疱及剧烈瘙痒性皮疹,始于脐周并蔓延至身体其他部位。沿真皮表皮交界处呈线性模式显示C3的直接免疫荧光检查可确诊PG。皮质类固醇仍然是治疗的选择,由于PG可能对胎儿产生不良影响,早期干预至关重要。我们报告一例PG病例并复习文献。

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引用本文的文献

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Phemphigoid gestationis.
BMJ Case Rep. 2018 Jun 17;2018:bcr-2018-225242. doi: 10.1136/bcr-2018-225242.

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