Wexham Park Hospital, Frimley Health NHS Foundation Trust, Berkshire, United Kingdom.
Wexham Park Hospital, Frimley Health NHS Foundation Trust, Berkshire, United Kingdom; University of Cyprus Medical School, Nicosia, Cyprus.
Am J Med Sci. 2020 Oct;360(4):406-409. doi: 10.1016/j.amjms.2020.05.023. Epub 2020 May 21.
Fahr's disease is a sporadic or familial neurodegenerative disorder characterized by symmetrical calcification of cerebral structures, particularly the basal ganglia, cerebellar dentate nuclei and surrounding white matter, in the absence of metabolic causes of calcification. We report the case of a previously fit, high functioning 58-year-old man who developed catastrophic irreversible neuropsychiatric collapse after sepsis despite appropriate antimicrobial treatment. Cranial computed tomography revealed extensive diffuse calcifications located in unusual areas. Laboratory studies excluded the presence of other pathologic processes leading to secondary intracranial calcification and a multigene panel failed to confirm mutations in the genes currently known to be associated with the disorder, supporting a diagnosis of sporadic Fahr's disease or idiopathic brain calcification. Important diagnostic considerations in the septic patient who develops neurological complications, namely sepsis-associated encephalopathy and antibiotic-associated encephalopathy, are discussed. The patient remains severely handicapped 6 months after the acute event. Patients with clinically silent neurodegenerative/neuropsychiatric conditions, such as Fahr's disease, may present with florid and unpredicted neurological features in the context of systemic illness.
Fahr 病是一种散发性或家族性神经退行性疾病,其特征为脑结构(特别是基底节、小脑齿状核和周围白质)对称性钙化,而无代谢性钙化原因。我们报告了一例先前身体状况良好、高功能的 58 岁男性,在败血症后发生灾难性、不可逆转的神经精神崩溃,尽管进行了适当的抗菌治疗。头颅计算机断层扫描显示广泛弥漫性钙化位于不常见的区域。实验室研究排除了其他导致继发性颅内钙化的病理过程的存在,并且多基因小组未能证实与该疾病相关的已知基因的突变,支持散发性 Fahr 病或特发性脑钙化的诊断。讨论了在发生神经系统并发症的败血症患者中的重要诊断考虑因素,即败血症相关脑病和抗生素相关脑病。急性事件发生 6 个月后,患者仍严重残疾。 Fahr 病等临床上无症状的神经退行性/神经精神疾病患者可能在系统性疾病的情况下出现明显且不可预测的神经特征。