Department of Neuropsychiatry, Wakayama Medical University, Wakayama, Japan.
Department of Neuropsychiatry, Wakayama Medical University, Wakayama, Japan.
Asian J Psychiatr. 2019 Jan;39:8-9. doi: 10.1016/j.ajp.2018.11.003. Epub 2018 Nov 13.
Autoimmune autonomic ganglionopathy (AAG) is a rare acquired immune-mediated disorder that leads to autonomic failure. It is sometimes complicated by mental and behavioral symptoms. We report a case of 72-year-old male with AAG who was admitted to the psychiatric department for prolonged severe delirium. Repeated loss of consciousness attributed to severe orthostatic hypotension disturbed recovery from delirium. In addition, intracerebral hemorrhage occurred during hospitalization, and this cerebrovascular event may have been substantially affected by unstable blood pressure due to AAG. This case suggests importance of differential diagnosis of AAG in patients with mental and behavioral symptoms accompanying severe autonomic failure.
自身免疫性自主神经节病变(AAG)是一种罕见的获得性免疫介导的疾病,可导致自主神经衰竭。它有时会伴有精神和行为症状。我们报告了一例 72 岁男性 AAG 病例,他因持续性严重谵妄而被收入精神科病房。反复因严重直立性低血压导致的意识丧失,影响了谵妄的恢复。此外,在住院期间发生了脑出血,而这种脑血管事件可能因 AAG 导致的血压不稳定而受到实质性影响。该病例提示,对于伴有严重自主神经衰竭的精神和行为症状的患者,需要进行 AAG 的鉴别诊断。