Recent developments in molecular genetics have expanded the spectrum of disorders
associated with pheochromocytomas (PCCs) and extra-adrenal paragangliomas (PGLs) …

Adrenal tumors mostly present with specific and unique clinical features, regarding their
endocrine metabolism. A 53-year-old man came to our Department for a left adrenal mass …

Adrenal neoplasms composed of more than one cell type and demonstrating a mixed
histologic appearance are exceedingly rare. We report the clinical and pathologic features of …

Mixed corticomedullary tumor (MCMT) of the adrenal gland is an extremely rare tumor
characterized by an admixture of steroidogenic cells and chromaffin cells in a single tumor …

Adrenal corticomedullary mixed tumors (CMMTs) are extremely rare; with only 20 cases
being reported to date, the pathogenesis has remained elusive. A 31-year-old woman …

Truly mixed corticomedullary tumors (MCMTs) are extremely rare and present as a single
tumor mass composed of an intimately admixed population of both adrenal cortical cells and …

Objective To report the case of a 78-year-old woman with mixed corticomedullary carcinoma
of the adrenal gland, and to review other reported lesions that exhibit clinical and/or …

Adrenal mixed corticomedullary tumors (MCMTs) are composed of an admixture of cortical
and medullary cells. Owing to the presence of two distinct components of different embryonic …

Mixed corticomedullary tumors (MCMTs) are rare and comprise medullary and cortical cells
in a single adrenal tumor. The mechanisms underlying their development have not been …

Background: Malignant mixed corticomedullary adrenal tumors (MCMTs) are extremely rare,
with limited cases reported in the literature. The pathophysiology of malignant MCMTs is not …