M. Karmakar, Debashis Dakshit, S. Saha, Arnab Bose
{"title":"异常大的颅咽管瘤1例","authors":"M. Karmakar, Debashis Dakshit, S. Saha, Arnab Bose","doi":"10.25259/crcr_52_2023","DOIUrl":null,"url":null,"abstract":"\n\nCraniopharyngiomas are benign slow-growing tumors of the central nervous system originating from squamous remnants of incompletely involuted craniopharyngeal duct. Craniopharyngiomas are said to be “giant” when they attain sizes of 5–6 cm or more.\n\n\n\nHere, we present a case of unusually large craniopharyngioma in a child, which, to the best of our knowledge, is the largest craniopharyngioma reported in the literature. The provisional diagnosis of craniopharyngioma was established using computed tomography and magnetic resonance imaging.\n\n\n\nCraniopharyngiomas are to be considered in the differentials for sellar and suprasellar region lesions causing mass effect. The provisional diagnosis is established by imaging but definitive diagnosis always requires histopathology.\n","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"38 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-06-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Unusually large craniopharyngioma: A case report\",\"authors\":\"M. Karmakar, Debashis Dakshit, S. Saha, Arnab Bose\",\"doi\":\"10.25259/crcr_52_2023\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\\n\\nCraniopharyngiomas are benign slow-growing tumors of the central nervous system originating from squamous remnants of incompletely involuted craniopharyngeal duct. Craniopharyngiomas are said to be “giant” when they attain sizes of 5–6 cm or more.\\n\\n\\n\\nHere, we present a case of unusually large craniopharyngioma in a child, which, to the best of our knowledge, is the largest craniopharyngioma reported in the literature. The provisional diagnosis of craniopharyngioma was established using computed tomography and magnetic resonance imaging.\\n\\n\\n\\nCraniopharyngiomas are to be considered in the differentials for sellar and suprasellar region lesions causing mass effect. The provisional diagnosis is established by imaging but definitive diagnosis always requires histopathology.\\n\",\"PeriodicalId\":419021,\"journal\":{\"name\":\"Case Reports in Clinical Radiology\",\"volume\":\"38 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-06-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Case Reports in Clinical Radiology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.25259/crcr_52_2023\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Case Reports in Clinical Radiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.25259/crcr_52_2023","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Craniopharyngiomas are benign slow-growing tumors of the central nervous system originating from squamous remnants of incompletely involuted craniopharyngeal duct. Craniopharyngiomas are said to be “giant” when they attain sizes of 5–6 cm or more.
Here, we present a case of unusually large craniopharyngioma in a child, which, to the best of our knowledge, is the largest craniopharyngioma reported in the literature. The provisional diagnosis of craniopharyngioma was established using computed tomography and magnetic resonance imaging.
Craniopharyngiomas are to be considered in the differentials for sellar and suprasellar region lesions causing mass effect. The provisional diagnosis is established by imaging but definitive diagnosis always requires histopathology.