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一例因癫痫发作而确诊的罕见法尔病病例。

A rare case of Fahr disease revealed by an epileptic seizure.

作者信息

Choayb Safaa, El Harras Yahya, Lahfidi Amal, Touarsa Firdaous, Fikri Meriem, Ech-Cherif El Kettani Najoua, Jiddane Mohamed

机构信息

Neuroradiology Department, Ibn Sina University Hospital Center, Rabat, Morocco.

出版信息

Radiol Case Rep. 2023 Mar 17;18(5):1954-1956. doi: 10.1016/j.radcr.2023.02.043. eCollection 2023 May.

Abstract

Fahr's disease is a rare neurodegenerative disorder, identified by bilateral and symmetrical intracerebral calcifications of mainly the basal ganglia. Patients often present extrapyramidal or neuropsychological symptoms. Seizure is one of the rarest manifestations that can reveal Fahr disease. We present the case of a 47-year-old male patient who had Fahr disease revealed by an inaugural tonic-clonic seizure.

摘要

法尔病是一种罕见的神经退行性疾病,主要表现为双侧对称性脑内钙化,以基底神经节为主。患者常出现锥体外系或神经心理症状。癫痫发作是法尔病最罕见的表现之一。我们报告一例47岁男性患者,首发强直阵挛性发作后被诊断为法尔病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6aa1/10030808/55f269e5cfa9/gr1.jpg

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