Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
Morika Suzuki, Takashi Watar. Endogenous Cushing's Syndrome Due to Right Adrenal Adenoma Presenting With Bilateral Leg Oedema and Skin Ulceration. Cureus. vol 16. issue 10. 2024-11-14. PMID:39525240. |
investigations revealed a low acth level, elevated urinary free cortisol, and a right adrenal mass, leading to the diagnosis of cs caused by an adrenal adenoma. |
2024-11-14 |
2024-11-17 |
Not clear |
Mohammad Reza Ghanbari Boroujeni, Elahe Meftah, Fatemeh Zarimeidani, Rahem Rahmati, Fatemeh Esfahania. Primary bilateral macronodular adrenal hyperplasia: A rare case report of Cushing syndrome and review of literature. Medicine. vol 103. issue 41. 2024-10-28. PMID:39465833. |
primary bilateral macronodular adrenal hyperplasia (pbmah) is a rare cause of acth-independent cushing syndrome (cs), accounting for <2% of cs cases. |
2024-10-28 |
2024-10-30 |
Not clear |
Huixin Zhou, Yaqi Yin, Peng Zhang, Binqi Li, Yuepeng Wang, Zhaohui Lyu, Weijun Gu, Yiming M. Long-term outcome of unilateral adrenalectomy for primary bilateral macronodular adrenal hyperplasia. Endocrine. 2024-10-09. PMID:39382825. |
primary bilateral macronodular adrenal hyperplasia (pbmah) is a form of cushing's syndrome (cs) characterized by heterogeneous cortisol secretion and clinical comorbidities. |
2024-10-09 |
2024-10-11 |
Not clear |
Laura Chioma, Giuseppa Patti, Marco Cappa, Mohamad Maghni. Cushing syndrome in paediatric population: who and how to screen. Journal of endocrinological investigation. 2024-09-30. PMID:39347909. |
according to the origin of the hypercortisolism, the acth-dependent form due to pituitary acth-secreting tumours is the most common form of endogenous cs in paediatric age (about 75-80% of cases), following by adrenal causes (about 15-20% of cases) including adenoma, carcinoma (which has a peak of incidence in the first decade), bilateral adrenal hyperplasia or carney complex, with a different distribution by age. |
2024-09-30 |
2024-10-02 |
Not clear |
Peng Yu, Haoyue Yuan, Xiaomu Li, Hong Che. Impact of cortisol on liver fat and metabolic health in adrenal incidentalomas and Cushing's syndrome. Endocrine. 2024-09-25. PMID:39320593. |
to evaluate liver fat content in patients with non-functional adrenal incidentalomas (nfai), mild autonomous cortisol secretion (macs), and cushing's syndrome (cs), and assess its relationship with cortisol levels. |
2024-09-25 |
2024-09-27 |
Not clear |
Kriti Joshi, Anna Taliou, Constantine A Strataki. Diagnostic and management challenges in paediatric Cushing's syndrome. Clinical endocrinology. 2024-08-16. PMID:39148300. |
endogenous cs is rare in the paediatric population and is caused mainly by tumours of the pituitary and adrenal glands, with ectopic sources being extraordinarily rare before the age of 18 years. |
2024-08-16 |
2024-08-18 |
Not clear |
Alexandra-Ioana Trandafir, Adina Ghemigian, Mihai-Lucian Ciobica, Claudiu Nistor, Maria-Magdalena Gurzun, Tiberiu Vasile Ioan Nistor, Eugenia Petrova, Mara Carsot. Diabetes Mellitus in Non-Functioning Adrenal Incidentalomas: Analysis of the Mild Autonomous Cortisol Secretion (MACS) Impact on Glucose Profile. Biomedicines. vol 12. issue 7. 2024-07-27. PMID:39062179. |
non-functioning adrenal incidentalomas (nfais) have been placed in relationship with a higher risk of glucose profile anomalies, while the full-blown typical picture of cushing's syndrome (cs) and associated secondary (glucocorticoid-induced) diabetes mellitus is not explicitly confirmed in this instance. |
2024-07-27 |
2024-07-29 |
Not clear |
Hideyasu Asai, Ikuo Yamamori, Shigeru Hagimoto, Kyoichi Okumura, Koki Sakakibar. Cushing's disease with twin pregnancy and diabetes mellitus: a case report and literature review. Endocrine journal. 2024-07-10. PMID:38987212. |
most reported cases of cs during pregnancy are of adrenal origin. |
2024-07-10 |
2024-07-13 |
Not clear |
Irene Tizianel, Mattia Barbot, Filippo Ceccat. Subtyping of Cushing's syndrome: a step ahead. Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association. 2024-04-04. PMID:38574761. |
after the description of the diagnostic tools available, we describe the characterization of functional non-neoplastic hypercortisolism (formerly known as pseudo-cushing state), then we report the subtyping of the different conditions of hypercortisolism: the differential diagnosis of acth-dependent forms and the management of adrenal hypercortisolism, with peculiar attention to the new genetic classification of adrenal cs, mild autonomous cortisol secretion and bilateral adrenal adenomas. |
2024-04-04 |
2024-04-07 |
Not clear |
Sisi Miao, Lin Lu, Shengyong Si, Dandan Peng, Ya Zhong, Zhijing Li, Zhenqiu Y. Clinical and cardiac characteristics of primary bilateral macronodular adrenal hyperplasia. Journal of medical biochemistry. vol 43. issue 1. 2024-03-18. PMID:38496019. |
primary bilateral macro-nodular adrenal hyperplasia (pbmah), is a rare cause of cs that is clinically distinct from the other common types of cs, but cardiac characteristics have been poorly studied. |
2024-03-18 |
2024-03-20 |
Not clear |
Yunjia Cai, Xue Zhao, Linan Ren, Siyuan Liu, Xinming Liu, Xiaokun Gang, Guixia Wan. Clinical features and risk factors for postoperative recurrence in patients with Cushing's syndrome of different etiologies. Scientific reports. vol 14. issue 1. 2024-02-28. PMID:38409302. |
the overall recurrence rate of cs caused by pituitary tumors and adrenal adenoma was 25.7%. |
2024-02-28 |
2024-03-01 |
Not clear |
Natasha Stoinis, Katherine Creeper, Jessica Phillips, Dorothy Graham, Ee Mun Li. Diverse presentations of Cushing's syndrome during pregnancy - A case series. The Australian & New Zealand journal of obstetrics & gynaecology. 2024-01-29. PMID:38284434. |
cushing's syndrome (cs) encompasses various causes of hypercortisolism including adrenocorticotropic hormone (acth) secreting pituitary adenoma with or without bilateral adrenal hyperplasia, an adrenal adenoma or carcinoma, ectopic acth or corticotrophin-releasing hormone (crh) secretion by a neoplasm or exogenous corticosteroid therapy. |
2024-01-29 |
2024-01-31 |
Not clear |
Valentina Guarnotta, Fabrizio Emanuele, Riccardo Salzillo, Carla Giordan. Adrenal Cushing's syndrome in children. Frontiers in endocrinology. vol 14. 2024-01-09. PMID:38192416. |
the most common causes of adrenal cs are hyperfunctioning adrenal tumours, adenoma or carcinoma. |
2024-01-09 |
2024-01-10 |
Not clear |
Valentina Guarnotta, Fabrizio Emanuele, Riccardo Salzillo, Carla Giordan. Adrenal Cushing's syndrome in children. Frontiers in endocrinology. vol 14. 2024-01-09. PMID:38192416. |
radiological imaging should be always combined with biochemical confirmatory tests, for the differential diagnosis of adrenal cs causes. |
2024-01-09 |
2024-01-10 |
Not clear |
Valentina Guarnotta, Fabrizio Emanuele, Riccardo Salzillo, Carla Giordan. Adrenal Cushing's syndrome in children. Frontiers in endocrinology. vol 14. 2024-01-09. PMID:38192416. |
treatment strategies for adrenal cs include surgery and in specific cases medical drugs. |
2024-01-09 |
2024-01-10 |
Not clear |
Shaobo Hu, Xianhua Wang, Fei Su, Qiong Zhou, Zhaoqing Li, Jie Luo, Huangying Ta. Effect of mitotane in patients with ectopic adrenocorticotropic hormone syndrome caused by advanced pancreatic neuroendocrine tumors: a case series and review of the literature. The Journal of international medical research. vol 52. issue 1. 2024-01-08. PMID:38190848. |
combination therapy with mitotane and other adrenal steroidogenesis inhibitors is common for patients with cushing's syndrome (cs). |
2024-01-08 |
2024-01-10 |
Not clear |
Anthony Parish, Clement Cheung, Anna Ryabets-Lienhard, Paul Zamiara, Mimi S Ki. Cushing Syndrome in Childhood. Pediatrics in review. vol 45. issue 1. 2023-12-31. PMID:38161162. |
he was diagnosed as having cushing syndrome (cs) due to primary pigmented nodular adrenocortical disease resulting in excess cortisol produced by the adrenal glands, leading to disruption of the hypothalamic-pituitary-adrenal axis. |
2023-12-31 |
2024-01-05 |
Not clear |
Anthony Parish, Clement Cheung, Anna Ryabets-Lienhard, Paul Zamiara, Mimi S Ki. Cushing Syndrome in Childhood. Pediatrics in review. vol 45. issue 1. 2023-12-31. PMID:38161162. |
long-term sequelae of cs, including adrenal insufficiency, obesity, hypertension, and mental health disorders, may remain despite definitive surgical treatment, meriting close follow-up with the primary care clinician and subspecialists. |
2023-12-31 |
2024-01-05 |
Not clear |
Betul Erdem, Muzeyyen Gonul, Ilknur Ozturk Unsal, Seyda Ozdemir Sahingo. Evaluation of psoriasis patients with long-term topical corticosteroids for their risk of developing adrenal insufficiency, Cushing's syndrome and osteoporosis. The Journal of dermatological treatment. vol 35. issue 1. 2023-12-29. PMID:38156462. |
in this study, we will investigate the possible side effects of psoriasis patients using long-term topical corticosteroids (tcs) such as adrenal insufficiency, cushing's syndrome (cs) and osteoporosis and determine how these side effects develop. |
2023-12-29 |
2023-12-31 |
Not clear |
Sharmilee Vetrivel, Mariangela Tamburello, Andrea Oßwald, Ru Zhang, Ali Khan, Sara Jung, Jessica E Baker, William E Rainey, Elisabeth Nowak, Barbara Altieri, Mario Detomas, Deepika Watts, Tracy Ann Williams, Ben Wielockx, Felix Beuschlein, Martin Reincke, Silviu Sbiera, Anna Rieste. PPARG dysregulation as a potential molecular target in adrenal Cushing's syndrome. Frontiers in endocrinology. vol 14. 2023-12-15. PMID:38098864. |
we performed a transcriptomic analysis of adrenal signaling pathways in various forms of endogenous cushing's syndrome (cs) to define areas of dysregulated and druggable targets. |
2023-12-15 |
2023-12-17 |
Not clear |