Idiopathic basal ganglia calcification presenting with obsessive‐compulsive symptoms: A case report

Daisuke Yoshioka, Takehiko Yamanashi, Kenta Taneda, Takashi Matsukawa, Kenta Orimo, Masaaki Iwata
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Abstract

Idiopathic basal ganglia calcification (IBGC), also known as Farh's disease, is a rare neurodegenerative disorder characterized by calcification of the basal ganglia and other brain regions. This disease usually occurs in middle‐aged patients and presents with various neurological and psychiatric symptoms. The exact prevalence is unknown; however, population genomic data analysis suggests a prevalence of at least 4.5/10,000 to 3.3/1000, indicating that the disease is more common than previously thought and remains underdiagnosed.We report the case of a middle‐aged Japanese man who attempted suicide twice because of obsessive‐compulsive ideation caused by trivial triggers. The patient's psychiatric symptoms resolved relatively quickly after hospitalization, and imaging and genetic testing led to a diagnosis of IBGC.This case report illustrates the importance of including IBGC in the differential diagnosis of psychiatric symptoms that initially develop in middle‐aged patients.
特发性基底节钙化伴有强迫症状:病例报告
特发性基底节钙化(IBGC)又称法氏病,是一种罕见的神经退行性疾病,以基底节和其他脑区钙化为特征。这种疾病通常发生在中年患者身上,表现为各种神经和精神症状。我们报告了一例日本中年男子的病例,他曾因琐事引发的强迫意念而两次试图自杀。本病例报告说明了将 IBGC 纳入中年患者最初出现的精神症状的鉴别诊断中的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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