{"title":"鞍区神经内分泌肿瘤(类癌型)与Rathke裂隙囊肿共存的研究一例病例报告及文献回顾","authors":"H. Mori","doi":"10.52768/2833-5465/1085","DOIUrl":null,"url":null,"abstract":"Intracranial Neuroendocrine Neoplasm (NET) is extremely rare. Herein, we report a very rare case of collision of primary NET (carcinoid type) and Rathkes cleft cysts (RCCs) in the sellar region. A 57-year-old man received a medical checkup and notified a possibility of pituitary neoplasm. However, he did not have any symptoms suggesting intracranial neoplasm, and kept follow up observation.","PeriodicalId":265928,"journal":{"name":"Journal of Clinical and Medical Surgery","volume":"31 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-04-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Coexistence of Neuroendocrine Neoplasm (Carcinoid Type) and Rathke’s Cleft Cysts in the Sella; A Case Report and Review of Literature\",\"authors\":\"H. Mori\",\"doi\":\"10.52768/2833-5465/1085\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Intracranial Neuroendocrine Neoplasm (NET) is extremely rare. Herein, we report a very rare case of collision of primary NET (carcinoid type) and Rathkes cleft cysts (RCCs) in the sellar region. A 57-year-old man received a medical checkup and notified a possibility of pituitary neoplasm. However, he did not have any symptoms suggesting intracranial neoplasm, and kept follow up observation.\",\"PeriodicalId\":265928,\"journal\":{\"name\":\"Journal of Clinical and Medical Surgery\",\"volume\":\"31 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-04-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Clinical and Medical Surgery\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.52768/2833-5465/1085\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Clinical and Medical Surgery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.52768/2833-5465/1085","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Coexistence of Neuroendocrine Neoplasm (Carcinoid Type) and Rathke’s Cleft Cysts in the Sella; A Case Report and Review of Literature
Intracranial Neuroendocrine Neoplasm (NET) is extremely rare. Herein, we report a very rare case of collision of primary NET (carcinoid type) and Rathkes cleft cysts (RCCs) in the sellar region. A 57-year-old man received a medical checkup and notified a possibility of pituitary neoplasm. However, he did not have any symptoms suggesting intracranial neoplasm, and kept follow up observation.