Leg ulcer in hereditary spherocytosis
Leg ulcer in hereditary spherocytosis
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DOI：
10.1046/j.1525-1470.2003.20512.x
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发表时间：
2003-09-01
影响因子：
1.5
通讯作者：
Neto, JF
中科院分区：
文献类型：
--
作者：
Giraldi, S;Abbage, KT;Neto, JF
惰性腿部溃疡是遗传性球形红细胞增多症患者罕见的并发症。我们报告了一名患有遗传性球形红细胞增多症的 13 岁女孩，她的内踝出现了慢性疼痛性溃疡。所有其他病因均被排除。脾切除九个月后，溃疡完全愈合，症状消失。我们讨论并回顾儿童中的这种不寻常的实体。
Indolent leg ulcers are a rare complication found in patients with hereditary spherocytosis. We report a 13-year-old girl with hereditary spherocytosis who developed a chronic painful ulcer on the medial malleolus. All other etiologies were ruled out. Nine months after splenectomy the ulcer healed completely and the symptoms disappeared. We discuss and review this unusual entity in children.