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类脂蛋白沉积症:特征性的临床和放射学表现。

Lipoid proteinosis: pathognomonic clinical and radiological features.

作者信息

Hegde Rahul Ganapati, Yadav Vikas K, Gajbhiye Meenakshi I

机构信息

Department of Radiology, Lokmanya Tilak Municipal Medical College and General Hospital, Mumbai, Maharashtra, India.

出版信息

BMJ Case Rep. 2014 Apr 10;2014:bcr2014203950. doi: 10.1136/bcr-2014-203950.

Abstract

A 22-year-old woman presented with a facial rash and hoarseness of voice. On examination, coarse waxy thickening and scarring was noted on the forehead and both the cheeks. The eyelid margins revealed a row of beaded papules termed 'moniliform blepharosis'. CT scan of the brain revealed bilateral, symmetric calcification of the amygdala of the hippocampal nuclei. This led to the diagnosis of lipoid proteinosis which is a rare genetic disorder.

摘要

一名22岁女性出现面部皮疹和声音嘶哑。检查时,在前额和双颊发现粗糙的蜡样增厚和瘢痕形成。眼睑边缘可见一排串珠状丘疹,称为“念珠状睑裂狭小”。脑部CT扫描显示海马核杏仁体双侧对称钙化。这导致诊断为类脂蛋白沉积症,这是一种罕见的遗传性疾病。

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本文引用的文献

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Amygdalae and striatum calcification in lipoid proteinosis.脑回沟回样钙质沉着症患者的杏仁核和纹状体钙化。
AJNR Am J Neuroradiol. 2010 Jan;31(1):88-90. doi: 10.3174/ajnr.A1699. Epub 2009 Aug 20.

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