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先天性球形红细胞增多症患者复发性溶血性贫血伴发小腿类丹毒
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作者 leverkus m. Schwaaf A. +1 位作者 Br?§unger T.m. 马慧群(译) 《世界核心医学期刊文摘(皮肤病学分册)》 2005年第6期12-12,共1页
A 29- year- old patient presented with recurrent erythematous eruptions on both lower legs of 15 years’duration. Family history, along with clinical and laboratory examinations, revealed congenital hereditary spheroc... A 29- year- old patient presented with recurrent erythematous eruptions on both lower legs of 15 years’duration. Family history, along with clinical and laboratory examinations, revealed congenital hereditary spherocytosis and excluded other reasons for the erythematous eruptions of the lower legs. During two subsequent episodes, we detected increased hemolysis that disappeared concomittantly on spontanous resolution of the lesions. To our knowledge, this case is the first report showing a recurrent erythematous eruption on the lower legs in a patient with congenital hereditary spherocytosis. These eruptions might be caused by intermittent hemolysis- induced inflammation as a result of the increased osmotic fragility of the erythrocytes and may evolve to chronic leg ulcers later in life. 展开更多
关键词 类丹毒 溶血性贫血 首例报道 红细胞脆性 慢性溃疡
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