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获得性肝脑变性

Acquired hepatocerebral degeneration.

作者信息

Yalcin Destina, Oguz-Akarsu Emel, Sokmen Mehmet

机构信息

Neurology Clinic, Umraniye Research and Training Hospital, Istanbul, Turkey. E-mail:

出版信息

Neurosciences (Riyadh). 2016 Apr;21(2):164-7. doi: 10.17712/nsj.2016.2.20150164.

Abstract

Acquired hepatocerebral degeneration is a rare, mostly irreversible neurological syndrome that occurs in patients with chronic liver disease, particularly in those with surgically or spontaneously induced portosystemic shunts. Typical magnetic resonance findings are T1 hyperintensity in the pallidum, substantia nigra, periaquaductal gray matter. In this paper, we report a case of a 51-year-old woman presented with hepatic encephalopathy episodes and typical magnetic resonance findings, who does not develop any neurological signs or symptoms, nor cognitive decline in the follow up period, lasting for 3 years.

摘要

获得性肝脑变性是一种罕见的、大多不可逆的神经综合征,发生于慢性肝病患者,尤其是那些有手术或自发形成的门体分流的患者。典型的磁共振表现为苍白球、黑质、导水管周围灰质T1高信号。在本文中,我们报告了一例51岁女性,出现肝性脑病发作及典型磁共振表现,在为期3年的随访期内未出现任何神经体征或症状,也无认知功能下降。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bff1/5107273/1f657d71d18a/Neurosciences-21-164-g001.jpg

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