作者: Luigi Mearini , Rachele Del Sordo , Elisabetta Costantini , Elisabetta Nunzi , Massimo Porena
DOI: 10.1159/000345141
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摘要: Introduction: Oncocytic neoplasms as tumors arising in the adrenal glands are rare, usually considered nonfunctional and benign. In current literature, there extremely limited reports of oncocytic neoplasms; to date, only 147 cases have been described. The rarity event prompted this study which reviews presents inci- dence, histology, diagnosis therapy oncocyt- ic neoplasms. Materials Methods: A review by system- atic literature search was done using MEDLINE /Cochrane libraries from 1950 date medical subject head- ings 'oncocytoma', 'adrenal gland', oncocytoma', neoplasm' carci- noma'. Results: Adrenal neoplasm is a rare dis- ease, incidentally detected because 17% functional masses. typical oncocyte displays abundant granular eosinophilic cytoplasm, due ac- cumulation mitochondria. Computed tomography magnetic resonance imaging not able identify or dif- ferentiate benign malignant mainstay adrenalectomy, recently performed laparoscopy. prognosis good for tumors, while adrenocortical carcinoma has poor surviv- al rate 5 years. Conclusions: neo-