{"title":"EVERY WHITE ON CT IS NOT BLEED: CASE REPORT OF A RARE, ATYPICAL WHITE EPIDERMOID TUMOR.","authors":"Harish Kumar, Divanshu Sharma, Aarti Narula, Navjot Singh, Preetnoor Kaur Nagra, Jasleen Kaur, Sandeep Singh","doi":"10.36106/ijar/9803843","DOIUrl":null,"url":null,"abstract":"Epidermoid tumors are benign congenital tumors within the neurosurgical domain, with white epidermoids constituting a\nrarer subset characterized by distinct radiological features. Here, we report the case of a 50-year-old female presenting\nwith recurrent headaches, initially misdiagnosed as an intracranial aneurysm but later revealed to be a sellar-originating white epidermoid tumor.\nDespite its size, conservative management was chosen due to the lesion's benign nature and lack of symptomatic contribution. White epidermoid\ntumors pose diagnostic challenges as they share radiological features with other intracranial lesions, including dermoid tumors, neuroenteric\ncysts, craniopharyngiomas, and clival tumors. Surgical resection carries a risk of chemical meningitis from tumor content leakage. Therefore,\naccurate preoperative diagnosis is imperative for appropriate management. In conclusion, white epidermoid tumors represent a rare variant\nrequiring meticulous radiological evaluation to ensure accurate diagnosis and optimal patient care.","PeriodicalId":13502,"journal":{"name":"Indian journal of applied research","volume":"62 14","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Indian journal of applied research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.36106/ijar/9803843","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
Epidermoid tumors are benign congenital tumors within the neurosurgical domain, with white epidermoids constituting a
rarer subset characterized by distinct radiological features. Here, we report the case of a 50-year-old female presenting
with recurrent headaches, initially misdiagnosed as an intracranial aneurysm but later revealed to be a sellar-originating white epidermoid tumor.
Despite its size, conservative management was chosen due to the lesion's benign nature and lack of symptomatic contribution. White epidermoid
tumors pose diagnostic challenges as they share radiological features with other intracranial lesions, including dermoid tumors, neuroenteric
cysts, craniopharyngiomas, and clival tumors. Surgical resection carries a risk of chemical meningitis from tumor content leakage. Therefore,
accurate preoperative diagnosis is imperative for appropriate management. In conclusion, white epidermoid tumors represent a rare variant
requiring meticulous radiological evaluation to ensure accurate diagnosis and optimal patient care.