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[一名患有重度甲型血友病的18日龄男婴自发性硬膜下血肿]

[Spontaneous subdural hematoma in a 18-day-old male newborn infant with severe hemophilia A].

作者信息

Ries M, Klinge J, Rauch R, Chen C, Deeg K H

机构信息

Klinik mit Poliklinik für Kinder und Jugendliche, Universität Erlangen-Nürnberg.

出版信息

Klin Padiatr. 1998 May-Jun;210(3):120-4. doi: 10.1055/s-2008-1043862.

Abstract

Most intracranial bleedings in hemophiliacs occur in patients more than 6 months of age. In the neonatal period, this complication is rare and almost always observed in the first week of life. Based on a review of the literature, intracranial hemorrhage is an exceedingly rare occurrence in infants with hemophilia aged 2 weeks-6 months. We report on a male infant with hemophilia A who was referred to our hospital on day 18 because of pallor and jaundice. The neurological examination was normal. A cerebral ultrasound showed a left sided subdural hematoma with a shift of the midline structures to the right. Packed red blood cells (10 ml/kg) and factor VIII replacement (250 IU) were rapidly instituted and a craniotomy with evacuation of the hematoma was performed. The postoperative course was uneventful. On discharge, the neurological examination was considered normal.

摘要

血友病患者的大多数颅内出血发生在6个月以上的患者中。在新生儿期,这种并发症很少见,几乎总是在出生后第一周出现。根据文献回顾,颅内出血在2周龄至6个月龄的血友病婴儿中极为罕见。我们报告了一名患有甲型血友病的男婴,他在出生第18天因面色苍白和黄疸被转诊至我院。神经系统检查正常。脑部超声显示左侧硬膜下血肿,中线结构向右移位。迅速输注浓缩红细胞(10 ml/kg)和补充凝血因子VIII(250 IU),并进行了开颅血肿清除术。术后过程顺利。出院时,神经系统检查被认为正常。

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