Zala Naman, Wirth Lena, Jordan Berit, Meredig Hagen, Rizos Timolaos
Department of Neurology, Heidelberg University Hospital, Im Neuenheimer Feld 400, Heidelberg 69120, Germany.
Department of Neuroradiology, Heidelberg University Hospital, Im Neuenheimer Feld 400, Heidelberg 69120, Germany.
Case Rep Neurol Med. 2021 May 12;2021:5517934. doi: 10.1155/2021/5517934. eCollection 2021.
Thunderclap headache is frequently associated with serious intracranial vascular disorders and a usual reason for emergency department admissions. Association of thunderclap headaches with autoimmune disorders, such as steroid-responsive encephalopathy with autoimmune thyroiditis (SREAT), is highly unusual. Here, we report a patient who presented with high-intensity headache of abrupt onset. Cerebrospinal fluid (CSF) analysis revealed moderate lymphocytic pleocytosis without evidence of infectious, neoplastic, or metabolic causes. Brain magnetic resonance imaging showed no specific pathologies, and examinations for neuronal antibodies in serum and CSF were negative. The medical history revealed that seven years before, an episode of an aseptic meningoencephalitis with remarkable response to steroids was present. Finally, increased levels of serum anti-TPO antibodies were identified, and against the background of a previous steroid-responsive aseptic meningoencephalitis, diagnosis of SREAT was highly probable. Methylprednisolone therapy was initiated, and the patient recovered completely. In particular, because most SREAT patients respond very well to steroids, this case underlines the importance of taking SREAT into consideration during the assessment of a high-intensity headache of abrupt onset.
霹雳样头痛常与严重的颅内血管疾病相关,是急诊科收治患者的常见原因。霹雳样头痛与自身免疫性疾病相关,如伴有自身免疫性甲状腺炎的类固醇反应性脑病(SREAT),这种情况非常罕见。在此,我们报告一名患者,其出现突发的高强度头痛。脑脊液(CSF)分析显示中度淋巴细胞增多,无感染、肿瘤或代谢原因的证据。脑磁共振成像未显示特定病变,血清和脑脊液中神经元抗体检测均为阴性。病史显示,七年前曾有一次无菌性脑膜脑炎发作,对类固醇有显著反应。最终,血清抗甲状腺过氧化物酶(anti-TPO)抗体水平升高,结合既往类固醇反应性无菌性脑膜脑炎病史,高度怀疑为SREAT。开始使用甲泼尼龙治疗,患者完全康复。特别是,由于大多数SREAT患者对类固醇反应良好,该病例强调了在评估突发高强度头痛时考虑SREAT的重要性。