Immunohistochemically ACTH positivity in an adrenal adenoma that mimicks pheochromocytoma in terms of clinical and radiological findings
FE Haydardedeoglu, GS Bagir, E Karadeli… - JCEM Case …, 2023 - academic.oup.com
Introduction Ectopic ACTH secretion is a rare cause of endogenous hypercortisolism.
Herein, a case of an immunhistochemically ACTH (+) adrenocortical adenoma with typical …
Herein, a case of an immunhistochemically ACTH (+) adrenocortical adenoma with typical …
Coexistence of adrenal cushing syndrome and pheochromocytoma in a “corticomedullary adenoma”: A case report and review of the literature
WY Ma, AH Yang, YH Chang, LY Lin… - The Endocrinologist, 2007 - journals.lww.com
Mixed pheochromocytoma and adrenal cortical adenoma (corticomedullary adenoma) is
extremely rare. We report a 41-year-old woman diagnosed preoperatively with Cushing …
extremely rare. We report a 41-year-old woman diagnosed preoperatively with Cushing …
[PDF][PDF] Corticomedullary mixed tumor of the adrenal gland
JA Wieneke, LDR Thompson… - Annals of diagnostic …, 2001 - academia.edu
Materials and Methods The records of three patients with tumors diagnosed as “mixed
corticomedullary adrenal tumors” were identified in the files of the Endocrine Registry at the …
corticomedullary adrenal tumors” were identified in the files of the Endocrine Registry at the …
Adrenal Cushing syndrome with detectable ACTH from an unexpected source
Mixed corticomedullary adrenal tumours (MCMT) are rare. We describe the second reported
case of a male patient presenting with hypertension and Cushing syndrome with MCMT. A …
case of a male patient presenting with hypertension and Cushing syndrome with MCMT. A …
Adrenocorticotropic Hormone-Producing Pheochromocytoma in a Patient with Adrenal Incidentaloma.
İ Anaforoğlu, A Livaoğlu… - … Research & Practice, 2024 - search.ebscohost.com
Pheochromocytomas are challenging and life-threatening neoplasms. They can secrete a
great variety of hormones and peptides apart from catecholamines. A case of …
great variety of hormones and peptides apart from catecholamines. A case of …
Adrenal cortical oncocytoma mimicking pheochromocytoma
A Kiriakopoulos, D Papaioannou, D Linos - Hormones, 2011 - Springer
OBJECTIVE: Adrenal tumors present with clinical features and signs unique to their specific
hormonal hypersecretion. However, there have been cases in which the clinical expression …
hormonal hypersecretion. However, there have been cases in which the clinical expression …
Mixed corticomedullary tumor accompanied by unilateral aldosterone-producing adrenocortical micronodules: A case report
S Yoshida, N Babaya, H Ito, Y Hiromine… - Journal of the …, 2021 - academic.oup.com
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 …
in a single adrenal tumor. The mechanisms underlying their development have not been …
[HTML][HTML] Composite adrenal medullary tumor: A rare cause of hypertension in a young male
S Menon, P Mahajan, SB Desai - Urology Annals, 2011 - journals.lww.com
Composite tumors of the adrenal medulla, containing pheochromocytoma and
ganglioneuroma, are rare. A 27-year-old male presented to us with dyspnea and was found …
ganglioneuroma, are rare. A 27-year-old male presented to us with dyspnea and was found …
[HTML][HTML] Mixed corticomedullary tumor of the adrenal gland
N Kimura, T Motoyama, J Saito… - Frontiers in …, 2022 - frontiersin.org
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 …
characterized by an admixture of steroidogenic cells and chromaffin cells in a single tumor …