Recurrent aphthous ulcers in Fanconi's anaemia: a case report
作者： Feyza Otan , Gokhan Acikgoz , Umur Sakallioglu , Burcu Ozkan
DOI: 10.1111/J.1365-263X.2004.00549.X
关键词: Oral ulcerations 、 Blood transfusion 、 Severe anaemia 、 Surgery 、 Increased haemoglobin 、 Medicine 、 Aphthous ulcerations 、 Neutropenia 、 Dermatology 、 Stomatitis 、 Fanconi's anaemia
摘要: Fanconi's anaemia (FA) is an autosomal recessive disorder that clinically characterized by aplastic anaemia, congenital malformations of the renal, cardiac, skeletal and skin structures, increased predisposition to malignancies. Patients with FA often present bleeding infection, which are symptoms related thrombocytopenia neutropenia. There few reports oral manifestations FA. We describe aphthous ulcerations in two siblings was a rapid improvement healing ulcers after blood transfusions haemoglobin levels. This may support role severe ulcerations.
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