Cohen Dylan T, Craven Catherine, Bragin Ilya
Neurology, St. Luke's University Health Network, Bethlehem, USA.
Neurology, Lewis Katz School of Medicine at Temple University, Philadelphia, USA.
Cureus. 2020 Jun 15;12(6):e8630. doi: 10.7759/cureus.8630.
The area postrema (AP) is a small, circumventricular organ located in the dorsal medulla and is characterized by an anastomosed capillary network with no blood-brain barrier. It contains the chemoreceptor trigger zone for vomiting, which is activated by noxious stimuli in the blood. Lesions to the AP produce a clinical syndrome referred to as area postrema syndrome (APS), which is characterized by intractable nausea, vomiting, and hiccups. APS manifests frequently as neuromyelitis optica spectrum disorders (NMOSD), where antibodies attack aquaporin-4 receptors, which are found in abundance in the AP. Its vascular supply is delivered by the anterior spinal artery or, at times, by small vessel branches of the vertebral artery itself. Ischemic stroke is the fifth leading cause of death in the United States; however, APS due to ischemic stroke has rarely been described. We present a case of a 62-year-old male with ischemic stroke in the cerebellum and brainstem, which produced intractable APS due to extension within his AP. He was treated with metoclopramide 10 mg four times daily and ondansetron 8 mg every eight hours, which relieved his symptoms. Recognizing that the patient's intractable nausea and vomiting was attributable to AP involvement was valuable in limiting further extraneous workup and focusing on our medical management. Ischemic stroke should be considered in the differential for APS. Given the size of the AP, thin-cut high-resolution diffusion-weighted MRI is warranted in patients with clinical APS. Recognizing that intractable nausea and vomiting may be attributable to stroke is valuable in mitigating extraneous and ineffective medical management. The patient case we describe in our report further outlines these findings.
最后区(AP)是位于延髓背侧的一个小型室周器官,其特征是具有吻合的毛细血管网络且无血脑屏障。它包含呕吐化学感受器触发区,可被血液中的有害刺激激活。最后区受损会产生一种临床综合征,称为最后区综合征(APS),其特征为顽固性恶心、呕吐和打嗝。APS常表现为视神经脊髓炎谱系障碍(NMOSD),其中抗体攻击水通道蛋白4受体,这些受体在最后区大量存在。其血液供应由脊髓前动脉提供,有时也由椎动脉本身的小分支提供。缺血性中风是美国第五大死因;然而,由缺血性中风导致的APS很少被描述。我们报告一例62岁男性,其小脑和脑干发生缺血性中风,由于病变扩展至最后区而导致顽固性APS。他接受了每日4次、每次10毫克甲氧氯普胺和每8小时8毫克昂丹司琼的治疗,症状得到缓解。认识到患者的顽固性恶心和呕吐归因于最后区受累,对于限制进一步的无关检查并专注于我们的药物治疗很有价值。在鉴别APS时应考虑缺血性中风。鉴于最后区的大小,对于有临床APS的患者,有必要进行薄层高分辨率扩散加权磁共振成像。认识到顽固性恶心和呕吐可能归因于中风,对于减少无关和无效的医疗管理很有价值。我们报告中描述的患者病例进一步概述了这些发现。