Linear IgA bullous dermatosis with desquamative gingivitis: A case report and literature review

被引：0

作者：

Kashima, Kana ^{[1
]}

Morita, Yoshihiro ^{[1
]}

Suzuki, Mao ^{[1
]}

Kinosada, Hiroko ^{[1
]}

Matsumiya-Matsumoto, Yuka ^{[1
]}

Kato, Itsuro ^{[1
]}

Matsunaga, Kazuhide ^{[1
]}

Uzawa, Narikazu ^{[1
]}

机构：

[1] Osaka Univ, Dept Oral & Maxillofacial Surg 2, Grad Sch Dent, 1-8 Yamadaoka, Suita, Osaka 5650871, Japan

来源：

JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY MEDICINE AND PATHOLOGY | 2022年 / 34卷 / 06期

关键词：

Linear IgA bullous dermatosis; LAD; Desquamative gingivitis; Bullous lesions of the skin; Intractable pemphigoid; DISEASE;

D O I：

10.1016/j.ajoms.2022.05.001

中图分类号：

R78 [口腔科学];

学科分类号：

1003 ;

摘要：

Linear IgA bullous dermatosis (LAD) is a rare chronic autoimmune disorder. As oral mucosal involvement is particularly rare, it is difficult to make a definitive diagnosis based on the oral lesions. This disorder mainly causes blisters on the skin of the whole body and may cause erosions in the oral cavity. It is characterized by linear IgA deposition on the epithelial basement membrane. This report presents a case of a refractory oral mucosal lesion that led to the diagnosis and cure of linear IgA bullous dermatosis.

引用

页码：845 / 849

页数：5

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