Results 61 to 70 of about 3,076 (170)
A pheochromocytoma case diagnosed as adrenal incidentaloma
The Turkish Journal of Pediatrics, 2017 There are two problems that needs to be addressed in cases of an adrenal incidentaloma. The first is to decide whether the adrenal mass is benign or malignant, and the second is to determine whether the mass is hormonally active or not.
Doğuş Vurallı +7 more
doaj +1 more source
Pheochromocytoma Across the Perioperative Course: Current Concepts and Clinical Management
Anesthesiology Research and Practice, Volume 2026, Issue 1, 2026.Pheochromocytoma is an uncommon neuroendocrine tumor with myriad nonspecific clinical presentations. If not recognized and treated, it is associated with the development of target organ damage and complications such as myocarditis, cardiomyopathy, cerebrovascular accidents, and diabetes mellitus, among numerous others. The pheochromocytoma diagnosis is
Aibek E. Mirrakhimov +2 more
wiley +1 more source
Batı Karadeniz Tıp Dergisi, 2017 Adrenal incidentalomas are often discovered incidentally after an imaging procedure unrelated to the adrenal gland. A patient with an accessory spleen as an adrenal incidentaloma was reported with current endocrine and radiological evaluations. A 53-year-
Taner Bayraktaroğlu, Abdurrahim Duşak
doaj
Journal of Clinical and Translational Science, 2017 OBJECTIVES/SPECIFIC AIMS: To compare methods of ascertaining prevalence for adrenal incidentalomas METHODS/STUDY POPULATION: Retrospective electronic medical record study using Looking Glass Clinical Analytics (Streamline Health, Atlanta, GA, USA) at an ...
Michio Taya +3 more
doaj +1 more source
Case Reports in Endocrinology, Volume 2026, Issue 1, 2026.Cushing syndrome (CS) is a rare endocrine disorder often overlooked in obese patients. Diagnosis of CS post bariatric surgery represents an emerging clinical concern with potentially severe consequences. A 26‐year‐old Saudi female presented with inadequate weight loss following sleeve gastrectomy.
Aishah Ekhzaimy +2 more
wiley +1 more source
A Rare Cavernous Hemangioma of the Adrenal Gland
Urology Case Reports, 2015 Adrenal cavernous hemangiomas are rare nonfunctioning benign tumors. This case report presents a patient with a huge nonfunctioning adrenal cavernous hemangioma presenting as an adrenal incidentaloma suspicious for adrenal myelolipoma.
Cheng Pang, Pengjie Wu, Gang Zhu
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Case Reports in Endocrinology, Volume 2026, Issue 1, 2026.Introduction Bilateral macronodular adrenocortical disease (BMAD) is an uncommon cause of endogenous Cushing syndrome, often diagnosed through bilateral adrenal incidentalomas without clinical manifestations of hypercortisolism. Mutations in the armadillo repeat-containing 5 (ARMC5) gene represent one of the causes of this disease, frequently ...
Daniela M. Soares +6 more
wiley +1 more source
Case Reports in Oncological Medicine, Volume 2026, Issue 1, 2026.Ectopic adrenocorticotropic hormone (ACTH) syndrome (EAS) is most often a paraneoplastic manifestation of small‐cell lung cancer and is rare in lung adenocarcinoma. Its features include a cushingoid appearance, skin hyperpigmentation, muscle weakness, hypertension, glucose intolerance, hypokalemia, and metabolic alkalosis resulting from nonsuppressible,
Murat Ay +3 more
wiley +1 more source
Prevalence of adrenal masses in Japanese patients with type 2 diabetes mellitus
Diabetology & Metabolic Syndrome, 2010 Introduction To date, there have been no reports on the prevalence of adrenal masses in type 2 diabetic patients. The present study aimed to evaluate the prevalence of adrenal incidentaloma in type 2 diabetic patients in Japan.
Hiroi Naoki +6 more
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