This report describes a case of pituitary adenoma with interspersed adrenal cortical cells. The pituitary cells were confirmed to be corticotrophs with Tpit and adrenocorticotropic hormone immunohistochemistry, whereas the adrenal cortical cells were verified to be such with steroidogenic factor-1 (SF-1), inhibin, calretinin, and Melan A staining. The presence of normal adrenal cortical cells in the heterotopic location of the sella fulfills the definition of choristoma. The origin of adrenal cortical cells within a pituitary adenoma remains unexplained. The important role of SF-1 in both pituitary and adrenal cortex may explain a relationship that supports the possibility of an abnormal proliferation and differentiation of uncommitted mese...
A right adrenal tumor was found incidentally during abdominal computed tomography exam in a 51-year-...
Silent adrenocorticotrophic pituitary adenomas are nonfunctioning pituitary adenomas that express ad...
Introduction. Pheochromocytomas are rare neuroendocrine tumors that arise from sympathetic adrenomed...
Silent corticotroph tumors are composed of corticotroph cells, but do not manifest any biochemical o...
Silent corticotroph pituitary adenomas (SCA) are defined as pituitary adenomas showing positive stai...
Silent corticotroph adenomas (SCA) are rare pituitary tumors with histologic hallmarks of corticotro...
Corticotroph adenomas are extremely rare in children and adolescents. We present a 15-year-old boy w...
Copyright © 2012 Subramanian Kannan et al. This is an open access article distributed under the Crea...
Adrenal neoplasms composed of more than one cell type and demonstrating a mixed histologic appearanc...
Object Adrenocorticotropic hormone (ACTH) adenomas have been recognized as a more aggressive and inv...
Cushing’s syndrome and pheochromocytomas (PCCs) are associated with endocrine hypertension. Cortisol...
Adrenal cortical tumors constitute a heterogeneous group of neoplasms with distinct clinical, morpho...
A right adrenal tumor was found incidentally during abdominal computed tomography exam in a 51-year-...
Adrenal cortical adenomas occur in about 5% of the population while adrenal cortical carcinoma is a ...
The hormone content in Cushing-type non-functioning tumors of the adrenal glands was measured to be ...
A right adrenal tumor was found incidentally during abdominal computed tomography exam in a 51-year-...
Silent adrenocorticotrophic pituitary adenomas are nonfunctioning pituitary adenomas that express ad...
Introduction. Pheochromocytomas are rare neuroendocrine tumors that arise from sympathetic adrenomed...
Silent corticotroph tumors are composed of corticotroph cells, but do not manifest any biochemical o...
Silent corticotroph pituitary adenomas (SCA) are defined as pituitary adenomas showing positive stai...
Silent corticotroph adenomas (SCA) are rare pituitary tumors with histologic hallmarks of corticotro...
Corticotroph adenomas are extremely rare in children and adolescents. We present a 15-year-old boy w...
Copyright © 2012 Subramanian Kannan et al. This is an open access article distributed under the Crea...
Adrenal neoplasms composed of more than one cell type and demonstrating a mixed histologic appearanc...
Object Adrenocorticotropic hormone (ACTH) adenomas have been recognized as a more aggressive and inv...
Cushing’s syndrome and pheochromocytomas (PCCs) are associated with endocrine hypertension. Cortisol...
Adrenal cortical tumors constitute a heterogeneous group of neoplasms with distinct clinical, morpho...
A right adrenal tumor was found incidentally during abdominal computed tomography exam in a 51-year-...
Adrenal cortical adenomas occur in about 5% of the population while adrenal cortical carcinoma is a ...
The hormone content in Cushing-type non-functioning tumors of the adrenal glands was measured to be ...
A right adrenal tumor was found incidentally during abdominal computed tomography exam in a 51-year-...
Silent adrenocorticotrophic pituitary adenomas are nonfunctioning pituitary adenomas that express ad...
Introduction. Pheochromocytomas are rare neuroendocrine tumors that arise from sympathetic adrenomed...