Download full-text PDF |
Source |
|---|
Publication Analysis
Top Keywords
Similar Publications
Case Report: Thymic neuroendocrine tumor with metastasis to the breast causing ectopic Cushing's syndrome.
Front Oncol
February 2025
Department and Clinic of Endocrinology and Internal Medicine, Wroclaw Medical University, Wroclaw, Poland.
Ectopic adrenocorticotropic hormone secretion (EAS) is responsible for approximately 10%-18% of Cushing's syndrome cases. Thymic neuroendocrine tumors (NETs) comprise 5%-16% of EAS; therefore, they are very rare and the data about this particular tumors is scarce. We present a case of a 34-year-old woman with a rapid onset of severe hypercortisolism in April 2016.
View Article and Find Full Text PDFExploring the high prevalence, comorbidities, and indicators of mild autonomous cortisol secretion in primary aldosteronism: a cohort study and systematic review.
Hypertens Res
March 2025
Renal Division, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.
Emerging evidence has suggested a significant prevalence of mild autonomous cortisol secretion (MACS) among patients diagnosed with primary aldosteronism (PA). However, MACS's clinical characteristics and implications in PA patients remain largely unexplored. To investigate the prevalence, comorbidities, and indicators of MACS in PA patients, we conducted a retrospective cohort study including 874 PA patients with dexamethasone suppression test results in the Taiwan Primary Aldosteronism Investigators (TAIPAI) cohort between February 2011 and February 2024.
View Article and Find Full Text PDFA Rare Case of Duplication-Associated Childhood-Onset Primary Pigmented Nodular Adrenocortical Disease.
JCEM Case Rep
March 2025
Department of Endocrinology, MKCG Medical College and Hospital, Berhampur, Odisha 760004, India.
Primary pigmented nodular adrenocortical disease (PPNAD) is a rare but important cause of adrenocorticotropic hormone (ACTH)-independent Cushing syndrome (CS). It usually presents as cyclical CS in young adults. Childhood onset of PPNAD is exceedingly rare.
View Article and Find Full Text PDFARMC5 mutations in primary bilateral macronodular adrenal hyperplasia: a family case report.
BMC Med Genomics
March 2025
Department of Urology, The First Hospital of Shanxi Medical University, Taiyuan, China.
Background: Primary bilateral macronodular adrenal hyperplasia (PBMAH) is a rare cause of overt Cushing's syndrome (CS), which usually manifests as bilateral macronodular adrenal nodules and varying levels of cortisol secretion. Previous studies have shown that ARMC5 play a huge role in the occurrence of PBMAH, which may be inherited to family members and lead to more severe clinical symptoms. ARMC5 variants may be associated with meningiomas, which is also illustrated by our report.
View Article and Find Full Text PDFThin Skin in Cushing's Syndrome.
N Engl J Med
March 2025
Lausanne University Hospital, Lausanne, Switzerland.
Want AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!