Bullous pemphigoid in 65 years old female: a case report

I. M. Sanjaya, Putu Artana, Embun Dini Hari
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引用次数: 1

Abstract

Introduction: Bullous pemphigoid is an autoimmune disorder. The incidence of bullous pemphigoid has increased over time, current understanding regarding treatment and complication is an important issue considering the disease often occur in elderly resulting in high rates of morbidity to the patients. Aim of current case report is to describe the clinical relevance regarding symptom and treatment of bullous pemphigoid.Case presentation: A 65 years old female patient, came with chief complaints of bullae in abdominal region with itching and burning sensation in the ruptured bullae. Over time bullae spread in lower and upper extremity. Patient was admitted for four days with therapy intravenous steroids, oral antihistamine, and potent topical steroids. Patient was discharged from hospital in well condition.Conclusion: Bullous pemphigoid is an inflammatory autoimmune skin disease and usually result in good prognosis with adequate management.Keywords: autoimmune, bullous, pemphigoid, skin, disease. 
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65岁女性大疱性类天疱疮1例
大疱性类天疱疮是一种自身免疫性疾病。大疱性类天疱疮的发病率随着时间的推移而增加,目前对治疗和并发症的了解是一个重要的问题,因为这种疾病通常发生在老年人中,导致患者的发病率很高。本病例报告的目的是描述大疱性类天疱疮的症状和治疗的临床相关性。病例介绍:一名65岁女性患者,主诉为腹部大疱,大疱破裂后有瘙痒和烧灼感。随着时间的推移,大泡在下肢和上肢扩散。患者入院治疗4天,静脉注射类固醇、口服抗组胺药和有效的局部类固醇。病人出院时情况良好。结论:大疱性类天疱疮是一种炎症性自身免疫性皮肤病,治疗得当,预后良好。关键词:自身免疫,大疱性,类天疱疮,皮肤,疾病。
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