R. Andrew, Schniederjan Matthew, J. ChernJoshua, Appert Andrew, Myers Hannah, Brahma Barunashish, S. BlackwellLaura, R. BoydstonWilliam, Prahalad Sampath
{"title":"Intracranial Mass Lesion Caused by Inflammatory Pseudotumor: A Case Report and Discussion","authors":"R. Andrew, Schniederjan Matthew, J. ChernJoshua, Appert Andrew, Myers Hannah, Brahma Barunashish, S. BlackwellLaura, R. BoydstonWilliam, Prahalad Sampath","doi":"10.36959/595/416","DOIUrl":null,"url":null,"abstract":"Inflammatory pseudo tumors are uncommon lesions that may, on occasion, occupy the intracranial space. Their management is unstandardized. We present a case of skull-based inflammatory pseudotumor in a 14-year-old boy who presented with multiple cranial nerve palsies mimicking Gradenigo syndrome. This illustrative case and a review of the literature is presented to highlight noteworthy features of this rare condition. These include that inflammatory pseudotumor may be multifocal and biopsy of a more accessible, smaller lesion may prove diagnostic.","PeriodicalId":432995,"journal":{"name":"Journal of Pediatric Neurology and Neuroscience","volume":"63 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2021-05-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Pediatric Neurology and Neuroscience","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.36959/595/416","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Inflammatory pseudo tumors are uncommon lesions that may, on occasion, occupy the intracranial space. Their management is unstandardized. We present a case of skull-based inflammatory pseudotumor in a 14-year-old boy who presented with multiple cranial nerve palsies mimicking Gradenigo syndrome. This illustrative case and a review of the literature is presented to highlight noteworthy features of this rare condition. These include that inflammatory pseudotumor may be multifocal and biopsy of a more accessible, smaller lesion may prove diagnostic.