Acquired haemophilia heralded by bleeding into the oral mucosa in a patient with bullous pemphigoid, rheumatoid arthritis, and vitiligo

被引:27
作者
Patel, RS [1 ]
Harman, KE
Nichols, C
Burd, RM
Pavord, S
机构
[1] Leicester Royal Infirm, Dept Haemostasis & Thrombosis, Directorate Haematol, Leicester LE1 5WW, Leics, England
[2] Leicester Royal Infirm, Dept Dermatol, Leicester LE1 5WW, Leics, England
关键词
D O I
10.1136/pgmj.2005.036483
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Acquired haemophilia is rare and potentially fatal, with a mortality of 20% if left untreated. There is a strong association with other autoimmune diseases. This report describes a patient with rheumatoid arthritis, vitiligo, and bullous pemphigoid where the diagnosis of acquired haemophilia was made after an extensive bleed into a bullous lesion in the buccal mucosa. This case highlights some of the potential complications of acquired haemophilia and its treatment.
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页数:2
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