Results 71 to 80 of about 13,033 (245)

New evidences on the regulation of SF-1 expression by POD1/TCF21 in adrenocortical tumor cells

Clinics
OBJECTIVES: Transcription Factor 21 represses steroidogenic factor 1, a nuclear receptor required for gonadal development, sex determination and the regulation of adrenogonadal steroidogenesis.
Monica Malheiros França, Antonio M. Lerario, Maria Candida B.V. Fragoso, Claudimara Ferini Pacicco Lotfi   +3 more
doaj   +1 more source

Adrenocortical neoplasms in children: Treatment and outcomes

Journal of Indian Association of Pediatric Surgeons, 2022
Background: Adrenocortical tumors are rare tumors in children with a paucity of outcome data, especially in a resource-challenged setting. Materials and Methods: A retrospective study was conducted to evaluate the presentation, management, and outcomes ...
Vishesh Jain, Mehak Sehgal, Anjan Dhua, Sameer Bakhshi, Devasenathipathy Kandasamy, Kalaivani Mani, Rajni Sharma, Vandana Jain, Nikhil Tandon, Sandeep Agarwala   +9 more
doaj   +1 more source

Pneumoperitoneum in two cats treated with trilostane for hypercortisolism

Veterinary Record Case Reports, Volume 14, Issue 1, February 2026.
Abstract This report describes two cases of pneumoperitoneum in cats receiving treatment for hypercortisolism and diabetes mellitus. Both cats presented with abdominal distention and lethargy and diagnoses of pneumoperitoneum were radiographically confirmed.
Nicholas James Kelly, Armando Sánchez‐Lara, Mike E. Herrtage, Hannah Wong, Andre Kortum   +4 more
wiley   +1 more source

Emerging methods for subtype differentiation in primary aldosteronism

Journal of Internal Medicine, Volume 299, Issue 2, Page 178-195, February 2026.
Abstract Primary aldosteronism (PA) is a common cause of hypertension. Compared to patients with essential hypertension, untreated PA is associated with a two‐ to fourfold greater risk of cardiovascular disease, renal failure, and death. PA is caused by increased secretion of aldosterone from one adrenal gland in 30% of the patients and both adrenal ...
Oskar Ragnarsson, C. Christofer Juhlin, Tobias Åkerström, Per Dahlqvist, Henrik Falhammar, Per Hellman   +5 more
wiley   +1 more source

novel insights into the genetics and pathophysiology of adrenocortical tumors [PDF]

, 2015
International audienceAdrenocortical tumors (ACTs) are typically unilateral and can be classified as benign adrenocortical adenomas (ACAs) or malignant adrenocortical cancers (ACCs).
Drougat, Ludivine, Lefèvre, Lucile, Omeiri, Hanin, Ragazzon, Bruno   +3 more
core   +7 more sources

Preclinical Cushing's syndrome in adrenal incidentalomas [PDF]

, 1992
Adrenal tumors are usually diagnosed by clinical symptoms of hormone excess. The increasing use of ultrasound and computed tomography results in the detection of a substantial number of incidentally discovered adrenal tumors.
Allolio, B., Krestin, G. P., Nieke, J., Reincke, Martin, Saeger, W., Winkelmann, W.   +5 more
core  

Gene expression profiling of human adrenocortical tumors using complementary deoxyribonucleic Acid microarrays identifies several candidate genes as markers of malignancy. [PDF]

, 2005
International audienceThe aim of this study was to identify predictor sets of genes whose over- or underexpression in human sporadic adrenocortical tumors would help to identify malignant vs.
Baudin, Eric, Berger, François,, Bertagna, Xavier, Bertherat, Jérôme, Chabre, Olivier, Cherradi, Nadia, De Fraipont, Florence, Defaye, Geneviève, El Atifi, Michelle, Feige, Jean-Jacques, Gicquel, Christine, Houlgatte, Rémi, Le Moigne, Gwennaelle, Plouin, Pierre-François   +13 more
core   +4 more sources

Adrenal gland tumours. Different clinical presentations in three dogs: a case report

Veterinární Medicína, 2013
Three dogs were evaluated due to the presence of unilateral adrenal gland masses with or without clinical signs. Case 1 showed a unilateral non-functional adrenocortical adenoma, discovered accidentally while Case 2 presented a unilateral cortisol ...
A. Loste, M. Borobia, M. Borobia, D. Lacasta, M. Carbonell, A. Basurco, M.C. Marca   +6 more
doaj   +1 more source

Pure oestrogen-secreting feminizing adrenocortical adenoma. [PDF]

Archives of Disease in Childhood, 1977
A 6-year-old boy presented with gynaecomastia. There was no clinical or biochemical evidence of excessive androgenic or glucorticoid activity, but urinary oestrogen levels were raised. An adrenocortical adenoma, demonstrated by x-ray, was surgically removed. Oestrogen levels fell immediately.
E, Bhettay, F, Bonnici
openaire   +2 more sources

Co‐Occurrence of Endogenous and Exogenous Cushing's Syndromes: Does “Double Cushing Syndrome” Really Exist? A Case Report

Clinical Case Reports, Volume 13, Issue 11, November 2025.
ABSTRACT Double Cushing syndrome exists: exogenous steroid use can mask concurrent adrenal hypercortisolism. When symptoms persist and cortisol remains high after tapering or stopping prescribed glucocorticoids, an endogenous source is likely. Early recognition with ACTH testing, dexamethasone suppression, and adrenal imaging reduces misdiagnosis ...
Reza Amani‐Beni, Atiyeh Karimi Shervedani, Bahar Darouei, Matin Noroozi, Maryam Heidarpour   +4 more
wiley   +1 more source