Zobrazeno 1 - 10
of 320
pro vyhledávání: '"subclinical cushing's syndrome"'
Autor:
Haremaru Kubo, Ryota Wada, Naohiro Sekikawa, Yasuhisa Nomura, Mutsuo Yamada, Minoru Inoue, Naoki Hattori, Yuto Yamazaki, Kazuhiro Sugimoto
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
BackgroundMultiple endocrine neoplasia type 1 (MEN1) is a rare autosomal dominant disorder, accompanied by multiple endocrine neoplasms of the parathyroid, pancreas, pituitary, and other neoplasms in the adrenal glands. However, in some cases, patien
Externí odkaz:
https://doaj.org/article/2c7d8e513f634b0599ac0d15637c57e8
Publikováno v:
Zhongguo quanke yixue, Vol 27, Iss 15, Pp 1873-1877 (2024)
Background Subclinical Cushing's syndrome (SCS) is a common subtype of adrenal incidentaloma. There are few reports on the correlation between hyperglycemia and hypercortisone secretion and its postoperative change in SCS patients. Objective To asses
Externí odkaz:
https://doaj.org/article/4ee2311d5bb14760bbd433ffd8f0a7f4
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
IntroductionThe management of Mild Autonomous Cortisol Secretion (MACS) remains a topic of debate among clinicians, with differing opinions on the effectiveness of surgical intervention compared to conservative treatment methods. This meta-analysis p
Externí odkaz:
https://doaj.org/article/46e22982309c4d84aab2acb92927d1a6
Autor:
Mohamad Mehdi Khadembashiri, Shahrzad Mohseni, Hamid Harandi, Mahnaz Pejman Sani, Mohamad Amin Khadembashiri, Rasha Atlasi, SeyedAhmad SeyedAlinaghi, Mohammadreza Mohajeri- Tehrani, Bagher Larijani
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
ObjectiveThis systematic review and meta-analysis was conducted to compare the benefits of adrenalectomy and conservative treatment for comorbidities associated with mild autonomous cortisol secretion (MACS) in patients diagnosed with MACS.Background
Externí odkaz:
https://doaj.org/article/b4f163ae5614430592f3037683ae3c04
Publikováno v:
Biomolecular and Health Science Journal, Vol 6, Iss 2, Pp 157-161 (2023)
Pheochromocytoma is a catecholamine-producing tumor that originates from adrenal medullary chromaffin cells. It affects 1–8 per million people annually and accounts for 5% of adrenal incidentalomas. Here, we report a 62-year-old man with sudden exc
Externí odkaz:
https://doaj.org/article/4fc0b3a6305544dbb8e748c71c1ab0f0
Akademický článek
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Publikováno v:
The Journal of Clinical Hypertension, Vol 23, Iss 11, Pp 1987-1991 (2021)
Abstract Here, we report a case of unilateral adrenal aldosterone and cortisol co‐secreting adenoma. A 34‐year‐old man with a history of severe hypertension for one year was detected hypokalemia (2.42 mmol/L lowest) and unilateral adrenal mass
Externí odkaz:
https://doaj.org/article/033cc828a0204598b4ff82620bd181c2
Autor:
S.І. Rybakov
Publikováno v:
Mìžnarodnij Endokrinologìčnij Žurnal, Vol 17, Iss 6, Pp 503-512 (2021)
The literature review provides a definition of the essence of subclinical Cushing’s syndrome. Subclinical Cushing’s syndrome (subclinical hypercortisolism) is a pathological condition of the body characterized by an autonomous, excessive secretio
Externí odkaz:
https://doaj.org/article/c49a24aeb0b94824a9ca4a6b524a9784
Autor:
Lihua Hu, Wenjun Ji, Meiyu Guo, Tieci Yi, Jie Wang, Minghui Bao, Yusi Gao, Han Jin, Difei Lu, Wei Ma, Xiaoning Han, Jianping Li, Zhenfang Yuan
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 9 (2022)
Externí odkaz:
https://doaj.org/article/d2517d10e8a3455686ac8938cb483fcb
Akademický článek
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