先天性白血病AML-M1伴心包积液的自发性缓解

A. Bülbül, M. Dursun, Yıldız Yıldırmak, B. Akyol, Umut ZübarioÄlu, E. Ünal, Lida Bülbül, Selcen YaroÄlu KazancÄ, S. Uslu
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引用次数: 5

摘要

先天性白血病是一种非常罕见的儿童恶性肿瘤,预后较差。其发病率接近每500万活产1例。多数病例为急性髓母细胞白血病伴三体。临床表现通常为白细胞增多、瘀斑、瘀斑、皮肤结节、肝脾肿大及中枢神经系统症状。23天的女孩以黄斑丘疹性皮炎和肝脾肿大为主诉,诊断为AML M1。随访期间发现大量心包积液。本病例的提出是为了强调文献中偶尔出现的心包积液与先天性白血病无三体和白血病自发性缓解的罕见关联。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Spontaneous Remission in Congenital Leukemia AML-M1 with Pericardial Effusion
Congenital leukemia is a very rare malignancy of childhood with a poor prognosis. The incidence is nearly 1 in 5 million live births. The majority of cases are acute myeloblastic leukemia with trisomy. Clinical manifestations are usually leukocytosis, petechia, ecchymosis, cutaneous nodules, hepatosplenomegaly and central nervous system symptoms. 23-days old girl was presented with complaints of maculopapular dermatitis and hepatosplenomegaly diagnosed as AML M1. During the follow-up period massive pericardial effusion was detected. This case is presented due to emphasize the rare association of pericardial effusion with congenital leukemia without trisomy and spontaneous remission of leukemia that was occasionally appear in the literature.
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