Department of Neurosurgery, National Health Organization, Sendai Medical Center, Sendai, Miyagi, Japan; Department of Neurosurgery, Graduate School of Medicine, Tohoku University, Sendai, Miyagi, Japan.
Department of Neurosurgery, National Health Organization, Sendai Medical Center, Sendai, Miyagi, Japan; Department of Neurosurgery, Graduate School of Medicine, Tohoku University, Sendai, Miyagi, Japan.
World Neurosurg. 2020 Sep;141:64-68. doi: 10.1016/j.wneu.2020.06.013. Epub 2020 Jun 8.
Hiccups are a well-known short-term phenomenon in daily life. If they persist or become intractable, they may be a primary symptom of a disease. Recent studies identified the medulla oblongata as the neuroanatomic center of the hiccup reflex arc. In previous cases, an isolated lesion at the dorsal side of the medulla oblongata induced intractable hiccups.
We herein describe a patient with a perimedullary arteriovenous fistula (PMAVF) at the craniocervical junction who had intractable hiccups. A 70-year-old male presented with a 3-year history of intractable hiccups that continued for a few days every week. An initial examination failed to identify the underlying cause, and neither medicine nor self-treatment attenuated his symptoms. Intracranial T2-weighted magnetic resonance imaging showed a hyperintensity area within the dorsolateral medulla and flow voids along the dorsal side of the cervical spine. Angiography revealed PMAVF fed by the left C1 radiculomedullary artery. Obliteration of the fistula was performed, after which intractable hiccups had completely disappeared within 1 week.
This is the first case report of PMAVF at the craniocervical junction presenting with intractable hiccups that suggested a lesion in the dorsal side of the medulla. The mechanisms underlying hiccups are also discussed.
打嗝是日常生活中一种众所周知的短期现象。如果持续或变得难以控制,它们可能是疾病的主要症状。最近的研究确定延髓是打嗝反射弧的神经解剖中心。在以前的病例中,孤立的延髓背侧损伤可引起难治性打嗝。
我们在此描述了一例颅颈交界区的硬脊膜动静脉瘘(PMAVF)患者,其患有难治性打嗝。一名 70 岁男性,有 3 年难治性打嗝病史,每周持续数天。初步检查未能确定潜在病因,药物和自我治疗均未能缓解其症状。颅内 T2 加权磁共振成像显示延髓背外侧有一个高信号区,以及沿着颈椎背侧的血流空影。血管造影显示由左侧 C1 脊神经根动脉供血的 PMAVF。瘘管闭塞后,难治性打嗝在 1 周内完全消失。
这是首例颅颈交界区 PMAVF 引起难治性打嗝的病例报告,提示延髓背侧有病变。还讨论了打嗝的发生机制。