Results 81 to 90 of about 12,329 (213)

Preoperative workup in the assessment of adrenal incidentalomas: outcome from 282 consecutive laparoscopic adrenalectomies [PDF]

, 2013
Background: To confirm the efficacy of preoperative workup, the authors analyse the results of a multicentre study in a surgical series of patients diagnosed with an adrenal incidentaloma.
Annunziato Tricarico, Antonietta Palazzo, BIONDI, BERNADETTE, COLAO, ANNAMARIA, Francesco Corcione, Giovanni Conzo, Giulio Belli, Luigi Santini, Maurizio De Palma, MILONE, MARCO, MUSELLA, MARIO, Paolo Bianco, PIVONELLO, ROSARIO   +12 more
core   +2 more sources

Mitophagy and Ubiquitination Coordinate Context‐Specific Mitochondrial Quality Control and EMT/MET Plasticity to Drive Cancer Cell Invasion

Advanced Science, Volume 13, Issue 16, 18 March 2026.
Metastatic invasion emerges when tumor‐intrinsic programs and microenvironmental forces converge on mitochondrial quality control. A context‐stratified framework links mtROS, mtDNA integrity, mechanics and nutrient/oxygen cues to fission–fusion remodeling, mtUPR and mitophagy.
Bin‐Hsu Mao, Bo‐Kai Su, Ying‐Jan Wang, Ting‐Yuan Tu   +3 more
wiley   +1 more source

Rare Association Between Neurofibromatosis Type 1 and Adrenocortical Carcinoma

Clinical Case Reports, Volume 14, Issue 3, March 2026.
Axial slice CT abdomen pelvis with portal venous contrast, revealing a well circumscribed 22 × 20 × 22 mm left adrenocortical adenocarcinoma (ACC) in a patient with neurofibromatosis type 1 (NF1). ABSTRACT Although rare, adrenocortical carcinoma (ACC) should be considered in individuals with neurofibromatosis type 1 (NF1) presenting with adrenal ...
Zachary Pluim, Joseph Do Woong Choi, Benedict Kakala, Jessica Wong, Roderick Clifton‐Bligh, Mark Sywak, Julie Howle   +6 more
wiley   +1 more source

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

Delayed Clinical Manifestation of Malignant Potential in a Cortisol‐Secreting Adrenal Tumor Initially Diagnosed as Adenoma

IJU Case Reports, Volume 9, Issue 2, March 2026.
ABSTRACT Introduction Distinguishing adrenocortical carcinoma (ACC) from adenoma is often difficult, particularly in hormonally active tumors with borderline histologic features. Case Presentation A 55‐year‐old woman presented with abdominal distension and central obesity. Hormonal evaluation confirmed ACTH‐independent Cushing's syndrome.
Fumihiro Ito, Koki Kobayashi, Gaku Hayashi, Shunsuke Kamijo, Takashi Fujita   +4 more
wiley   +1 more source

Multiple endocrine neoplasia [PDF]

, 2017
Multiple endocrine neoplasia (MEN) describes the occurrence of tumours affecting two or more endocrine glands in one patient. Two main forms are recognized: MEN type 1 (MEN1) and type 2 (MEN2).
Newey, Paul J.
core   +2 more sources

Benign Adrenal Adenomas Are Associated With Reduced Prevalence of Hospitalised Patients With COVID‐19

Clinical Endocrinology, Volume 104, Issue 3, Page 207-214, March 2026.
ABSTRACT Introduction Adrenal incidentalomas (AI) are commonly found on imaging done for indications other than to assess the adrenal glands. Prevalence increases with age and is around 10% in people over 80 years. The majority of AIs are benign adenomas, with 20%−50% exhibiting mild autonomous cortisol secretion (MACS).
Alan Kelsall, Chris Johns, Eleanor Hills, Jenny Zhao, John Newell‐Price   +4 more
wiley   +1 more source

Primary pigmented nodular adrenocortical disease presenting with a unilateral adrenocortical nodule treated with bilateral laparoscopic adrenalectomy: a case report

Journal of Medical Case Reports, 2010
Introduction Primary pigmented nodular adrenocortical disease is a rare cause of adrenocorticotropic hormone-independent Cushing's syndrome. We report an uncommon primary pigmented nodular adrenocortical disease case presenting with a unilateral ...
Kaltsas Gregory, Chrysikos Dimosthenis T, Markou Athina, Avlonitis Spiros, Pappa Theodora, Zografos George N, Aggeli Chrysanthi, Piaditis George   +7 more
doaj   +1 more source

Luteinizing hormone (LH)-responsive Cushing's syndrome: the demonstration of LH receptor messenger ribonucleic acid in hyperplastic adrenal cells, which respond to chorionic gonadotropin and serotonin agonists in vitro [PDF]

, 2003
In a substantial part of adrenal adenomas and hyperplasias from patients with Cushing's syndrome, cortisol production is controlled by the expression of aberrant hormone receptors on adrenocortical cells.
Bonjer, H.J. (Jaap), Clark, A.J. (Adrian), Feelders, R.A. (Richard), Herder, W.W. (Wouter) de, Hofland, L.J. (Leo), Jong, F.H. (Frank) de, Koetsveld, P.M. (Peter) van, Lamberts, S.W.J. (Steven), Lely, A-J. (Aart-Jan) van der, Themmen, A.P.N. (Axel), Verhoef-Post, M. (Miriam)   +10 more
core   +4 more sources

Dermatologic Features of Endocrine Tumor Syndromes—Systematic Review and Meta‐Analysis

International Journal of Dermatology, Volume 65, Issue 3, Page 464-488, March 2026.
ABSTRACT Endocrine tumor syndromes, including multiple endocrine neoplasia types 1, 2A, and 2B (MEN1, MEN2A, MEN2B), Carney complex (CNC), and PTEN hamartoma tumor syndrome (PHTS), are hereditary conditions characterized by multisystem tumor development.
Sára Pálla, Zseraldin Metyovinyi, Fanni Adél Meznerics, Arash Mirzahosseini, Judit Tőke, Miklós Tóth, Henriett Butz, Attila Patócs, Márta Medvecz   +8 more
wiley   +1 more source