Symptomatic Intracranial Hypertension Secondary to Superior Vena Cava Thrombosis as the First Manifestation of Behçet’s Disease

Introduction: Behçet’s disease (BD) is a rare inflammatory autoimmune disorder characterized by recurrent oral and genital ulcers, uveitis, and other systemic manifestations. Reported neurological manifestations of BD include meningoencephalitis, cerebral venous thrombosis, intracranial hyperten...

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Main Authors: Payam Sadry, Rayan Magsi, Maahum Ahmed, Jennifer Amsdell, Talal Derani, Naeem Mahfooz, Ajaz Sheikh
Format: Article
Language:English
Published: The University of Toledo 2023-07-01
Series:Translation
Subjects:
Online Access:https://openjournals.utoledo.edu/index.php/translation/article/view/550
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author Payam Sadry
Rayan Magsi
Maahum Ahmed
Jennifer Amsdell
Talal Derani
Naeem Mahfooz
Ajaz Sheikh
author_facet Payam Sadry
Rayan Magsi
Maahum Ahmed
Jennifer Amsdell
Talal Derani
Naeem Mahfooz
Ajaz Sheikh
author_sort Payam Sadry
collection DOAJ
description Introduction: Behçet’s disease (BD) is a rare inflammatory autoimmune disorder characterized by recurrent oral and genital ulcers, uveitis, and other systemic manifestations. Reported neurological manifestations of BD include meningoencephalitis, cerebral venous thrombosis, intracranial hypertension (ICH), and cranial nerve palsies. Involvement of the superior vena cava (SVC) is rare but should be considered in patients with BD with suspected ICH. Case Report: A 32-year-old man presented with ICH as the initial manifestation of BD. He presented with a one-week history of facial and neck edema, headache, and blurry vision, followed by fever, sore throat, and oral blisters a few days later. Lumbar puncture (LP) was performed, and opening pressure was found to be elevated at >50 cmH2O and closing pressure of 36 cmH2O. The work-up included a chest CT, which identified thrombosis of the SVC extending into the brachiocephalic veins, and blood work which revealed elevated inflammatory markers. Further probing revealed a history of genital ulcers and a family history of a cousin with BD. The patient underwent mechanical thrombectomy and was treated with oral prednisone with symptom resolution. Conclusion: BD has a wide spectrum of symptomology and may present without common manifestations, making it challenging to diagnose. The aim of our report was to emphasize the importance exploring the rarer vascular, neurological, and cardiac symptoms of BD in order to avoid potentially dangerous sequala. A system approach may be necessary to diagnose and optimally treat these patients.
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spelling doaj.art-eb1f20ce524b48c7b06d4716e32203cd2023-07-07T09:18:32ZengThe University of ToledoTranslation2469-67062023-07-0111210.46570/utjms.vol11-2023-550Symptomatic Intracranial Hypertension Secondary to Superior Vena Cava Thrombosis as the First Manifestation of Behçet’s DiseasePayam Sadry0Rayan Magsi1Maahum Ahmed2Jennifer Amsdell3Talal Derani4Naeem Mahfooz5Ajaz Sheikh6University of Toledo Department of NeurologyUniversity of Toledo Department of NeurologyUniversity of Toledo Department of NeurologyUniversity of Toledo Department of NeurologyOak Clinic for Multiple SclerosisUniversity of Toledo Department of NeurologyUniversity of Toledo Department of Neurology Introduction: Behçet’s disease (BD) is a rare inflammatory autoimmune disorder characterized by recurrent oral and genital ulcers, uveitis, and other systemic manifestations. Reported neurological manifestations of BD include meningoencephalitis, cerebral venous thrombosis, intracranial hypertension (ICH), and cranial nerve palsies. Involvement of the superior vena cava (SVC) is rare but should be considered in patients with BD with suspected ICH. Case Report: A 32-year-old man presented with ICH as the initial manifestation of BD. He presented with a one-week history of facial and neck edema, headache, and blurry vision, followed by fever, sore throat, and oral blisters a few days later. Lumbar puncture (LP) was performed, and opening pressure was found to be elevated at >50 cmH2O and closing pressure of 36 cmH2O. The work-up included a chest CT, which identified thrombosis of the SVC extending into the brachiocephalic veins, and blood work which revealed elevated inflammatory markers. Further probing revealed a history of genital ulcers and a family history of a cousin with BD. The patient underwent mechanical thrombectomy and was treated with oral prednisone with symptom resolution. Conclusion: BD has a wide spectrum of symptomology and may present without common manifestations, making it challenging to diagnose. The aim of our report was to emphasize the importance exploring the rarer vascular, neurological, and cardiac symptoms of BD in order to avoid potentially dangerous sequala. A system approach may be necessary to diagnose and optimally treat these patients. https://openjournals.utoledo.edu/index.php/translation/article/view/550Behcet's DiseaseNeuro-Behcet DiseaseSVC SyndromeICH
spellingShingle Payam Sadry
Rayan Magsi
Maahum Ahmed
Jennifer Amsdell
Talal Derani
Naeem Mahfooz
Ajaz Sheikh
Symptomatic Intracranial Hypertension Secondary to Superior Vena Cava Thrombosis as the First Manifestation of Behçet’s Disease
Translation
Behcet's Disease
Neuro-Behcet Disease
SVC Syndrome
ICH
title Symptomatic Intracranial Hypertension Secondary to Superior Vena Cava Thrombosis as the First Manifestation of Behçet’s Disease
title_full Symptomatic Intracranial Hypertension Secondary to Superior Vena Cava Thrombosis as the First Manifestation of Behçet’s Disease
title_fullStr Symptomatic Intracranial Hypertension Secondary to Superior Vena Cava Thrombosis as the First Manifestation of Behçet’s Disease
title_full_unstemmed Symptomatic Intracranial Hypertension Secondary to Superior Vena Cava Thrombosis as the First Manifestation of Behçet’s Disease
title_short Symptomatic Intracranial Hypertension Secondary to Superior Vena Cava Thrombosis as the First Manifestation of Behçet’s Disease
title_sort symptomatic intracranial hypertension secondary to superior vena cava thrombosis as the first manifestation of behcet s disease
topic Behcet's Disease
Neuro-Behcet Disease
SVC Syndrome
ICH
url https://openjournals.utoledo.edu/index.php/translation/article/view/550
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