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浅表性铁沉积症:一例罕见的共济失调和耳神经学表现病例。

Superficial siderosis: A rare case of ataxia and otoneurological manifestations.

作者信息

Assarzadegan Farhad, Ehsanpour Elaheh, Hosseini Behnam, Beladi-Moghadam Nahid, Mansouri Behnam, Hesami Omid

机构信息

Imam Hossein Hospital, Department of Neurology, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

出版信息

Iran J Neurol. 2013;12(2):69-71.

Abstract

Superficial siderosis (SS) is a rare disease which affects people in all ages and both sexes, but three times more in men. Pathological etiology is deposition of hemosiderin (a product of the breakdown of blood) in leptomeninges, subpial layer, ependymal surface and other parts of central nervous system (CNS) and typically leads to neurological dysfunction and progressive irreversible signs and symptoms. We present a 33-year-old man with complete deafness in left ear, partial hearing loss in right ear, gait imbalance, bilateral frontotemporal throbbing headache and anosmia resulted from superficial siderosis.

摘要

浅表性铁沉积症(SS)是一种罕见疾病,可累及各年龄段和两性人群,但男性患者是女性患者的三倍。其病理病因是含铁血黄素(血液分解产物)沉积于软脑膜、软膜下层、室管膜表面及中枢神经系统(CNS)的其他部位,通常会导致神经功能障碍以及进行性不可逆的体征和症状。我们报告一名33岁男性,因浅表性铁沉积症导致左耳完全失聪、右耳部分听力丧失、步态失衡、双侧额颞部搏动性头痛和嗅觉丧失。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a285/3829287/d65c7e3951cf/IJNL-12-069-g001.jpg

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