{"title":"Case 349: Venous Infarction Secondary to Hypoglossal Canal Dural Arteriovenous Fistula.","authors":"Matheus Hideki Taborda, Matheus Kahakura Franco Pedro, Bernardo Corrêa de Almeida Teixeira","doi":"10.1148/radiol.252118","DOIUrl":null,"url":null,"abstract":"<p><p>History A 76-year-old man presented to the emergency department with a 1-month history of worsening binocular diplopia on left horizontal gaze, along with 1 week of progressive dysarthria and dizziness. Additionally, he had a chronic history of right-sided cervicobrachialgia related to degenerative disk disease, which had been improving with oral analgesia. The patient's past medical history included hypertension, dyslipidemia, insomnia, and hypothyroidism. He also had postpolio syndrome affecting the right lower limb. He reported no fever, chills, cough, shortness of breath, abdominal pain, or chest pain. There was no history of rash, intravenous drug use, immunosuppressive medication use, or documented congenital abnormalities. He reported no recent or recurrent bacterial or viral infections. At clinical examination, the patient appeared tired and had a decreased level of alertness. He was hypertensive (165/91 mm Hg) but had a normal body temperature. Other vital signs were unremarkable. Neurologic assessment revealed left abducens nerve palsy, right lower facial palsy, horizontal nystagmus during right eye adduction, and right lower limb paresis with ipsilateral patellar hyperreflexia. Brain MRI performed the day after admission showed imaging abnormalities. Laboratory testing showed an elevated C-reactive protein level (135 mg/L; upper limit of normal, 1 mg/L); other blood tests were within normal limits. Extensive additional diagnostic workup-including serologic testing for anti-aquaporin-4 antibody, anti-DNA antibody, lupus anticoagulant, antinuclear antibody, anti-cardiolipin antibody, and rheumatoid factor-yielded negative results. Lumbar puncture revealed a normal cerebrospinal fluid opening pressure (18 cm H<sub>2</sub>O; upper limit of normal, 25 cm H<sub>2</sub>O). The cerebrospinal fluid was clear, with a normal total nucleated cell count (3.75/mm<sup>3</sup>; reference range, 0-5/mm<sup>3</sup>), normal glucose level (53 mg/dL [2.9 mmol/L]; reference range, 50-77 mg/dL [2.8-4.3 mmol/L]), and elevated total protein level (750 mg/L; reference range, 100-450 mg/L). Cerebrospinal fluid oligoclonal bands were positive.</p>","PeriodicalId":20896,"journal":{"name":"Radiology","volume":"320 2","pages":"e252118"},"PeriodicalIF":17.6000,"publicationDate":"2026-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Radiology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1148/radiol.252118","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING","Score":null,"Total":0}
引用次数: 0
Abstract
History A 76-year-old man presented to the emergency department with a 1-month history of worsening binocular diplopia on left horizontal gaze, along with 1 week of progressive dysarthria and dizziness. Additionally, he had a chronic history of right-sided cervicobrachialgia related to degenerative disk disease, which had been improving with oral analgesia. The patient's past medical history included hypertension, dyslipidemia, insomnia, and hypothyroidism. He also had postpolio syndrome affecting the right lower limb. He reported no fever, chills, cough, shortness of breath, abdominal pain, or chest pain. There was no history of rash, intravenous drug use, immunosuppressive medication use, or documented congenital abnormalities. He reported no recent or recurrent bacterial or viral infections. At clinical examination, the patient appeared tired and had a decreased level of alertness. He was hypertensive (165/91 mm Hg) but had a normal body temperature. Other vital signs were unremarkable. Neurologic assessment revealed left abducens nerve palsy, right lower facial palsy, horizontal nystagmus during right eye adduction, and right lower limb paresis with ipsilateral patellar hyperreflexia. Brain MRI performed the day after admission showed imaging abnormalities. Laboratory testing showed an elevated C-reactive protein level (135 mg/L; upper limit of normal, 1 mg/L); other blood tests were within normal limits. Extensive additional diagnostic workup-including serologic testing for anti-aquaporin-4 antibody, anti-DNA antibody, lupus anticoagulant, antinuclear antibody, anti-cardiolipin antibody, and rheumatoid factor-yielded negative results. Lumbar puncture revealed a normal cerebrospinal fluid opening pressure (18 cm H2O; upper limit of normal, 25 cm H2O). The cerebrospinal fluid was clear, with a normal total nucleated cell count (3.75/mm3; reference range, 0-5/mm3), normal glucose level (53 mg/dL [2.9 mmol/L]; reference range, 50-77 mg/dL [2.8-4.3 mmol/L]), and elevated total protein level (750 mg/L; reference range, 100-450 mg/L). Cerebrospinal fluid oligoclonal bands were positive.
期刊介绍:
Published regularly since 1923 by the Radiological Society of North America (RSNA), Radiology has long been recognized as the authoritative reference for the most current, clinically relevant and highest quality research in the field of radiology. Each month the journal publishes approximately 240 pages of peer-reviewed original research, authoritative reviews, well-balanced commentary on significant articles, and expert opinion on new techniques and technologies.
Radiology publishes cutting edge and impactful imaging research articles in radiology and medical imaging in order to help improve human health.