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一名患有严重血友病的新生儿脾破裂——病例报告及文献复习

Splenic rupture in a newborn with severe hemophilia--case report and review.

作者信息

Tengsupakul Supatida, Sedrak Aziza, Freed Jennifer, Martinez-Carde Lynda, Fireman Fernando, Pierre Louisdon, Sadanandan Swayam

机构信息

Department of Pediatrics, The Brooklyn Hospital Center, Brooklyn, NY 11201, USA.

出版信息

J Pediatr Hematol Oncol. 2010 May;32(4):323-6. doi: 10.1097/MPH.0b013e3181d640ae.

Abstract

Life-threatening splenic rupture is rare in neonates with severe hemophilia. There are only 3 cases of splenic rupture in neonates with hemophilia reported in the literature. We present the case of an infant, born to a hemophilia A carrier mother. The infant was asymptomatic until discharge at 48 hours of age, but presented on the third day of life with shock, abdominal distension, and severe anemia. Computed tomography of the abdomen confirmed the diagnosis of splenic rupture with hemoperitoneum. The infant recovered after extensive supportive care surgery and factor replacement.

摘要

危及生命的脾破裂在患有严重血友病的新生儿中很少见。文献中仅报道了3例血友病新生儿脾破裂病例。我们报告一例婴儿,其母亲为甲型血友病携带者。该婴儿在48小时龄出院前无症状,但在出生后第三天出现休克、腹胀和严重贫血。腹部计算机断层扫描证实诊断为脾破裂伴腹腔积血。经过广泛的支持性护理手术和凝血因子替代治疗后,婴儿康复。

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