患有严重联合免疫缺陷及短肢骨骼发育异常的婴儿发生恶性B细胞淋巴瘤。
Malignant B-cell lymphoma in an infant with severe combined immunodeficiency with short-limbed skeletal dysplasia.
作者信息
van den Berg H, Wage K, Burggraaf J D, Peters M
机构信息
Department of Pediatric Oncology, Emma kinderziekenhuis AMC, University of Amsterdam, The Netherlands.
出版信息
Acta Paediatr. 1997 Jul;86(7):778-80. doi: 10.1111/j.1651-2227.1997.tb08588.x.
Abstract
In an infant with skeletal anomalies and haemolytic disease, intestinal perforation was caused by necrosis of an as yet undetected B-cell lymphoma. Severe combined immunodeficiency with short-limbed skeletal dysplasia was diagnosed. This is the first published report of a patient with this syndrome in combination with haemolytic disease and B-cell-lymphoma.
摘要
在一名患有骨骼异常和溶血性疾病的婴儿中，肠道穿孔是由一种尚未被发现的B细胞淋巴瘤坏死所致。诊断为重度联合免疫缺陷伴短肢骨骼发育不良。这是首例关于该综合征合并溶血性疾病和B细胞淋巴瘤患者的发表报告。
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