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Case Report and Review of Literature: Patient with Malignant Pheochromocytoma
2019
Journal:  
Ankara Üniversitesi Tıp Fakültesi Mecmuası
Author:  
DOI:  
10.4274/atfm.galenos.2019.85570
Abstract:

Pheochromocytomas are catecholamine-secreting neuroendocrine tumors that arise from chromaffin cells of the adrenal medulla. At least 10 percent of pheochromocytomas are malignant. A diagnosis of malignant pheochromocytoma can only be made by identifying tumor deposits in tissues that do not normally contain chromaffin cells. The clinical course of malignat pheochromocytoma is highly variable, with reported five-year survival rates that range widely from 12 to 84 percent. We report a rare case of a 38-year-old female who have malignant pheochromocytoma. We review the classic and current literature regarding management of this uncommon tumor.

Keywords:

Case Report and Review of Literature: Patient with Malignant Pheochromocytoma
2019
Journal:  
Ankara Üniversitesi Tıp Fakültesi Mecmuası
Author:  
DOI:  
10.4274/atfm.galenos.2019.85570
Abstract:

Pheochromocytomas are catecholamine-secreting neuroendocrine tumors that arise from the chromaffin cells of the adrenal medulla. At least 10 percent of pheochromocytomas are malignant. A diagnosis of malignant pheochromocytoma can only be made by identifying tumor deposits in tissues that do not normally contain chromaffin cells. The clinical course of malignant pheochromocytoma is highly variable, with five-year survival rates that range widely from 12 to 84 percent. We report a rare case of a 38-year-old woman who has malignant pheochromocytoma. We review the classic and current literature regarding management of this uncommon tumor.

Keywords:

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Ankara Üniversitesi Tıp Fakültesi Mecmuası

Field :   Sağlık Bilimleri

Journal Type :   Ulusal

Metrics
Article : 1.037
Cite : 25.078
2023 Impact : 0.191
Details
Ankara Üniversitesi Tıp Fakültesi Mecmuası