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表现为胆汁淤积和新生儿肝衰竭的IV型法伯病:两例报告

Farber's disease type IV presenting with cholestasis and neonatal liver failure: report of two cases.

作者信息

Willis Asha, Vanhuse Cherie, Newton Kimberly P, Wasserstein Melissa, Morotti Raffaella A

机构信息

Department of Pediatrics and Pediatric Hepatology, Mount Sinai School of Medicine, New York, NY 10029, USA.

出版信息

Pediatr Dev Pathol. 2008 Jul-Aug;11(4):305-8. doi: 10.2350/07-08-0318.1. Epub 2007 Sep 28.

Abstract

We report 2 siblings diagnosed with Farber's disease type IV. Type IV is a subtype of Farber's disease that presents in the neonatal period and usually initially lacks the triad of symptoms, including painful and deformed joints, subcutaneous nodules, and hoarse cry, classically seen in the other subtypes. While it is well known that all neonates with type IV present with hepatomegaly, a previously unrecognized presentation is that of cholestatic jaundice and rapidly evolving liver failure. We describe 2 siblings who presented with jaundice in the neonatal period and discuss the clinical data and variation in pathologic findings that should be considered for the diagnosis.

摘要

我们报告了2例被诊断为IV型法伯病的同胞患儿。IV型是法伯病的一种亚型,在新生儿期发病,通常最初缺乏其他亚型中典型出现的三联征症状,包括关节疼痛和畸形、皮下结节及哭声嘶哑。虽然众所周知所有IV型新生儿均有肝肿大,但一种此前未被认识到的表现是胆汁淤积性黄疸和迅速进展的肝衰竭。我们描述了2例在新生儿期出现黄疸的同胞患儿,并讨论了诊断时应考虑的临床数据及病理结果差异。

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