Oliver Gibb, Jacob W Lucas, Sujay Deshpande, Daniel C Edwards
{"title":"伪装成卵巢肿瘤的巨大副神经节瘤:一个独特的遗传来源不明的副神经节瘤病例。","authors":"Oliver Gibb, Jacob W Lucas, Sujay Deshpande, Daniel C Edwards","doi":"10.1080/08998280.2024.2448639","DOIUrl":null,"url":null,"abstract":"<p><p>Paraganglioma and pheochromocytoma are rare tumors originating from chromaffin cells: pheochromocytoma from within the adrenal gland and paraganglioma from the sympathetic chain in the retroperitoneum. Though many are clinically silent, both classically present with hyperadrenergic symptoms. We present a case of a patient with an immense retroperitoneal mass found to be a clinically silent paraganglioma. The unusual size and presentation of the tumor as well as its undetermined genetic origin give a unique perspective into this rare tumor.</p>","PeriodicalId":8828,"journal":{"name":"Baylor University Medical Center Proceedings","volume":"38 4","pages":"555-557"},"PeriodicalIF":0.0000,"publicationDate":"2025-01-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12233688/pdf/","citationCount":"0","resultStr":"{\"title\":\"Massive paraganglioma masquerading as ovarian tumor: a unique case of paraganglioma of undetermined genetic origin.\",\"authors\":\"Oliver Gibb, Jacob W Lucas, Sujay Deshpande, Daniel C Edwards\",\"doi\":\"10.1080/08998280.2024.2448639\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Paraganglioma and pheochromocytoma are rare tumors originating from chromaffin cells: pheochromocytoma from within the adrenal gland and paraganglioma from the sympathetic chain in the retroperitoneum. Though many are clinically silent, both classically present with hyperadrenergic symptoms. We present a case of a patient with an immense retroperitoneal mass found to be a clinically silent paraganglioma. The unusual size and presentation of the tumor as well as its undetermined genetic origin give a unique perspective into this rare tumor.</p>\",\"PeriodicalId\":8828,\"journal\":{\"name\":\"Baylor University Medical Center Proceedings\",\"volume\":\"38 4\",\"pages\":\"555-557\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-01-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12233688/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Baylor University Medical Center Proceedings\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1080/08998280.2024.2448639\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q3\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Baylor University Medical Center Proceedings","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/08998280.2024.2448639","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
Massive paraganglioma masquerading as ovarian tumor: a unique case of paraganglioma of undetermined genetic origin.
Paraganglioma and pheochromocytoma are rare tumors originating from chromaffin cells: pheochromocytoma from within the adrenal gland and paraganglioma from the sympathetic chain in the retroperitoneum. Though many are clinically silent, both classically present with hyperadrenergic symptoms. We present a case of a patient with an immense retroperitoneal mass found to be a clinically silent paraganglioma. The unusual size and presentation of the tumor as well as its undetermined genetic origin give a unique perspective into this rare tumor.