[Senear-Usher syndrome (seborrheic pemphigus): An exceptional case].

Q3 Medicine
Juan David Galán-Lozano, Julio César Velasco-Castro, Lorena García-Agudelo, Ledmar Jovanny Vargas-Rodríguez
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引用次数: 0

Abstract

Background: Among the autoimmune diseases causing erosive lesions and blisters on skin and mucous membranes is pemphigus. Within this is a rare subtype known as seborrheic pemphigus or Senear-usher syndrome which is characterized by broken blisters and crusts involving the seborrheic areas.

Case report: A 40-year-old female patient, initially treated in a first level unit for a condition of 45 days of evolution, characterized by thick scabby lesions with an erythematous base, pruritic and painful, located in the center of the face, with posterior extension towards the abdomen, thorax, and extremities. Treatment consisted of prednisolone, with favorable evolution. The biopsy of the lesions with the diagnosis of seborrheic pemphigus.

Conclusions: Senear-usher syndrome is a rare disease of multifactorial origin. Early diagnosis and adequate treatment are decisive factors to avoid the evolution and advanced forms of the disease.

[Senear-Usher综合征(脂溢性天疱疮):一个特例]。
背景:天疱疮是引起皮肤和粘膜糜烂性病变和水泡的自身免疫性疾病之一。这是一种罕见的亚型,称为脂溢性天疱疮或Senear-usher综合征,其特征是涉及脂溢性区域的破碎水泡和结痂。病例报告:一名40岁女性患者,最初在一级病房治疗,病情发展45天,特征是厚痂状病变,基部红斑,瘙痒和疼痛,位于面部中心,后向腹部、胸部和四肢延伸。治疗以强的松龙为主,进展良好。诊断为脂溢性天疱疮的病变活检。结论:Senear-usher综合征是一种罕见的多因素发病。早期诊断和适当治疗是避免疾病发展和发展的决定性因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Revista alergia Mexico
Revista alergia Mexico Medicine-Immunology and Allergy
CiteScore
0.70
自引率
0.00%
发文量
9
审稿时长
16 weeks
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