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一名16岁女孩患出血性、大疱性过敏性紫癜,此前未诊断出显性营养不良性大疱性表皮松解症。

Hemorrhagic, bullous Henoch Schonlein purpura in a 16-year-old girl with previously undiagnosed dominant dystrophic epidermolysis bullosa.

作者信息

Abdulla Farah, Sheth Anita P, Lucky Anne W

机构信息

Department of Dermatology, University of Cincinnati, Cincinnati, Ohio 45229-3039, USA.

出版信息

Pediatr Dermatol. 2010 Mar-Apr;27(2):203-4. doi: 10.1111/j.1525-1470.2010.01105.x.

Abstract

A 16-year-old girl presenting with systemic and cutaneous symptoms of hemorrhagic Henoch-Schonlein purpura continued to develop bullae on top of old scars. Past history was significant for bullae on the feet and legs after trauma. Based on history, physical examination, disease course, and biopsy, the patient, her mother, and other family members were diagnosed with dominant dystrophic epidermolysis bullosa, explaining the severe course and complications of her Henoch-Schonlein purpura.

摘要

一名16岁女孩表现出出血性过敏性紫癜的全身和皮肤症状,旧疤痕上不断出现大疱。既往史显示,外伤后足部和腿部曾出现大疱。根据病史、体格检查、病程及活检结果,患者、其母亲及其他家庭成员被诊断为显性营养不良性大疱性表皮松解症,这解释了她过敏性紫癜的严重病程及并发症。

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