دورية أكاديمية
An Ecchordosis Physaliphora, a Rare Entity, Involving the Central Nervous System: A Systematic Review of the Literature
العنوان: | An Ecchordosis Physaliphora, a Rare Entity, Involving the Central Nervous System: A Systematic Review of the Literature |
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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 |
تدمد: | 20358377 |
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DOI: | 10.3390/neurolint15040075 |