دورية أكاديمية

NeuroBehcet’s-related intracranial hypertension without cerebral venous thrombosis: case report and review of literature

التفاصيل البيبلوغرافية
العنوان: NeuroBehcet’s-related intracranial hypertension without cerebral venous thrombosis: case report and review of literature
المؤلفون: Jinesh Mukesh Shah, Warren Fong, Deidre Anne De Silva
المصدر: BMC Neurology, Vol 24, Iss 1, Pp 1-8 (2024)
بيانات النشر: BMC, 2024.
سنة النشر: 2024
المجموعة: LCC:Neurology. Diseases of the nervous system
مصطلحات موضوعية: Behcet’s disease, NeuroBehcet’s, Intracranial pressure, Cerebral venous thrombosis, Idiopathic intracranial hypertension, Tocilizumab, Neurology. Diseases of the nervous system, RC346-429
الوصف: Abstract Background We present a rare case of NeuroBehcet’s-related intracranial hypertension without cerebral venous thrombosis (NBrIHwCVT), occurring as the first presentation of NeuroBehcet’s. In addition, we describe the novel use of subcutaneous tocilizumab for this indication. This is followed by a review of the literature on this topic. Case The patient was a 28-year-old lady of Southern Chinese origin with a known history of Behcet’s disease with oral ulcers and ocular findings for which she was on mycophenolate mofetil and adalimumab. She presented with a headache and bilateral disc swelling associated with an intracranial pressure (ICP) of > 40cmH20. There were no structural lesions or cerebral venous thrombosis (CVT) on imaging. Initial lumbar puncture had raised leucocytes and protein. We discuss diagnostic challenges given persistently elevated ICP despite subsequent non-inflammatory cerebrospinal fluid (CSF) profiles and non-response to acetazolamide. She eventually showed a response to immunosuppressant therapy in the form of pulsed methylprednisolone, cyclophosphamide and subsequently subcutaneous tocilizumab, supporting the diagnosis of NBrIHwCVT. Complete normalization of ICP remains challenging. Her disease course was severe, unusual for her ethnicity. Literature review We identified 34 patients (including ours) from 14 publications. We found that the majority of NBrIHwCVT patients were young (average age of 34 years), with a slight female preponderance. Of the 17 cases in the literature with available data on CSF profile, none had raised leucocytes whilst one patient had elevated protein. Patients were generally treated with steroids and occasionally azathioprine, in line with the suspected autoimmune pathophysiology. Of 22 patients with data on outcome, six (27%) were noted to have recurrence of symptoms generally occurring a few months later. Conclusion As demonstrated by this case, NBrIHwCVT can present with BD with raised ICP even if there is no prior history of NB, central Asian ethnicity, cerebral venous thrombosis or features of inflammation on the CSF. We demonstrated how novel use of Tocilizumab may have a role in the management of NBrIHwCVT. Based on our literature review, patients were more likely to be young, female, display a non-inflammatory CSF picture, be treated with steroids and harbour a possibility of recurrence.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1471-2377
العلاقة: https://doaj.org/toc/1471-2377Test
DOI: 10.1186/s12883-024-03708-x
الوصول الحر: https://doaj.org/article/20ea5493f9404a449222963a0f8b15e7Test
رقم الانضمام: edsdoj.20ea5493f9404a449222963a0f8b15e7
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:14712377
DOI:10.1186/s12883-024-03708-x