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| PubMed | |
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Article by Li,S.Z |
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Article by Zuo,Y.G |
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��ժҪ�� ����Դ����Ա�Ƥ�ɽ�֢��һ�����������Դ�����Ƥ�������䷢������Ƥ?��Ƥ���ӵ�ê˿��Ҫ�ɷ֢��ͽ�ԭ�����������йء�����Դ����Ա�Ƥ�ɽ�֢������ۼ�Ƥ�����Ĥ����Ҫ���ֶ����ı�Ƥ��ˮ�壬����������������ή�����ۡ���������Խ��Խ����о�֤ʵ���ò��ɺϲ�����Ƥ�����Լ�����ϵͳ�Լ�������������ϵͳ���������������Լ������ڷ���ϵͳ��������Ⱦ�Լ�����ѪҺϵͳ�����Լ������Լ��������ֺϲ�������Ϊ��������������һЩ������ػ��Ƶ��о���
Complications of epidermolysis bullosa acquisita
Li Sizhe, Zuo Yagang Department of Dermatology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China Corresponding author: Zuo Yagang, Email: zuoyagang@263.net ��Abstract�� Epidermolysis bullosa acquisita ��EBA�� is a rare kind of autoimmune blistering disease associated with autoimmunity to type �� collagen, which is the major component of anchoring fibrils at the dermal?epidermal junction. EBA may involve the mucous membrane and skin, and mainly manifests as diverse subepidermal blisters leaving milia and atrophic scars after healing. Recently, it has been described in association with a number of other skin and systemic diseases, including gastrointestinal diseases, autoimmune diseases, endocrine diseases, infectious diseases, hematological diseases and neoplastic diseases. Some of the complications were described in case reports, and some were investigated about the relevant pathogenesis.
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