دورية أكاديمية

An Ecchordosis Physaliphora, a Rare Entity, Involving the Central Nervous System: A Systematic Review of the Literature

التفاصيل البيبلوغرافية
العنوان: An Ecchordosis Physaliphora, a Rare Entity, Involving the Central Nervous System: A Systematic Review of the Literature
المؤلفون: Rajesh K. Gupta, Thejasvi A. Reddy, Ashutosh Gupta, Rohan Samant, Carlos A. Perez, Anam Haque
المصدر: Neurology International, Vol 15, Iss 4, Pp 1200-1211 (2023)
بيانات النشر: MDPI AG, 2023.
سنة النشر: 2023
المجموعة: LCC:Medicine
LCC:Internal medicine
LCC:Neurosciences. Biological psychiatry. Neuropsychiatry
مصطلحات موضوعية: ecchordosis physaliphora, notochord, chordoma, CNS, Medicine, Internal medicine, RC31-1245, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571
الوصف: Ecchordosis physaliphora (EP) is a benign notochordal remnant, which is often an incidental finding; however, it can rarely present with neurological symptoms. We performed a systematic review of the literature for cases of symptomatic EP published in PubMed, Web of Science and Embase from January 1982 to May 2023. This is the largest review to date and revealed 60 cases including ours. Headache (55%) and CSF rhinorrhea (32%) were the most frequent clinical manifestations. The majority of symptomatic EP lesions were located in the prepontine region (77%) and required surgical resection (75%). EP should be considered in patients with neurologic symptoms in the setting of prepontine or posterior sphenoid sinus lesions. While symptomatic patients often require surgical intervention, rare cases may respond to oral corticosteroids.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2035-8377
Relation: https://www.mdpi.com/2035-8377/15/4/75; https://doaj.org/toc/2035-8377
DOI: 10.3390/neurolint15040075
URL الوصول: https://doaj.org/article/ef1f9cdcbe934487beea395755758f87
رقم الأكسشن: edsdoj.f1f9cdcbe934487beea395755758f87
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:20358377
DOI:10.3390/neurolint15040075