Kitamura Taisuke, Gotoh Seiji, Takaki Hayato, Kiyuna Fumi, Yoshimura Sohei, Fujii Kenichiro
Department of Cerebrovascular Disease, Fukuoka Red Cross Hospital.
Rinsho Shinkeigaku. 2016 Jul 28;56(7):499-503. doi: 10.5692/clinicalneurol.cn-000884. Epub 2016 Jun 30.
An 86-year-old woman with a one-year history of dementia was admitted to our hospital complaining of loss of appetite, hallucinations, and disturbance of consciousness. She gradually presented with chorea-like involuntary movements of the extremities. Diffusion-weighted magnetic resonance imaging (MRI) showed bilateral symmetrical hyperintense signals in the basal ganglia. The serum vitamin B12 level was below the lower detection limit of 50 pg/ml. The homocysteine level was markedly elevated at 115.8 nmol/ml. Anti-intrinsic factor and anti-parietal cell antibody tests were positive. Gastrointestinal endoscopy revealed atrophic gastritis. The patient was diagnosed with encephalopathy due to vitamin B12 deficiency caused by pernicious anemia. Involuntary movements and MRI abnormalities improved with parenteral vitamin B12 supplementation. Bilateral basal ganglia lesions are rare manifestations of adult vitamin B12 deficiency. The present case is considered valuable in identifying the pathophysiology of involuntary movement due to vitamin B12 deficiency.
一名患有痴呆症病史一年的86岁女性因食欲不振、幻觉和意识障碍入住我院。她逐渐出现四肢舞蹈样不自主运动。弥散加权磁共振成像(MRI)显示基底节区双侧对称性高信号。血清维生素B12水平低于50 pg/ml的检测下限。同型半胱氨酸水平显著升高,达115.8 nmol/ml。抗内因子和抗壁细胞抗体检测呈阳性。胃肠内镜检查显示萎缩性胃炎。该患者被诊断为恶性贫血所致维生素B12缺乏性脑病。补充肠外维生素B12后,不自主运动和MRI异常得到改善。双侧基底节病变是成人维生素B12缺乏的罕见表现。本病例对于明确维生素B12缺乏所致不自主运动的病理生理学具有重要价值。