• Keisuke Sasaki, Tomoo Inoue, Yasuo Nishijima, Takashi Inoue, Shinsuke Suzuki, Toshiki Endo, Masayuki Ezura, Hiroshi Uenohara, and Teiji Tominaga.
• Department of Neurosurgery, National Hospital Organization, Sendai Medical Center, Miyagino-ku, Sendai, Miyagi, Japan; Department of Neurosurgery, Tohoku University, Graduate School of Medicine, Aoba-ku, Sendai, Miyagi, Japan.
• World Neurosurg. 2020 Apr 1; 136: 157-160.

BackgroundSpinal dural arteriovenous fistulas (DAVFs) are usually associated with neurologic dysfunction adjacent to the shunt point; however, the symptoms are uncommon far from the site of the fistula. To our knowledge, this is the first report of a patient with rapidly progressive isolated pseudobulbar palsy because of thoracic DAVF.Case DescriptionWe report a patient with thoracic DAVF presenting with remote symptoms of brainstem congestion. The patient was a 36-year-old man who presented with a sudden history of vomiting, dysphagia, and flaccid weakness in the 4 limbs. Intracranial magnetic resonance (MR) imaging at a local hospital demonstrated T2 signal hyperintensity within the medulla, and he was referred to our hospital for a suspected brainstem lesion. However, cervical MR imaging revealed a dilated and tortuous perimedullary venous plexus, and spinal angiography revealed DAVF in T5-6 with a feeding artery from the intercostal artery. After obliteration of the fistula, the progression of the disease was stopped and the symptoms improved.ConclusionsAlthough rare, thoracic DAVFs may present symptoms resembling brainstem infarction. Prompt surgical intervention is necessary for patients with thoracic DAVF presenting with rapidly progressive pseudobulbar palsy.Copyright © 2020 Elsevier Inc. All rights reserved.

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