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Quoted phrase not found in phrase index: "ACTH-independent macronodular adrenal hyperplasia 1"
Page 1
Diagnosis and management of primary bilateral macronodular adrenal hyperplasia.
Vassiliadi DA, Tsagarakis S. Vassiliadi DA, et al. Endocr Relat Cancer. 2019 Oct 1;26(10):R567-R581. doi: 10.1530/ERC-19-0240. Print 2019 Oct 1. Endocr Relat Cancer. 2019. PMID: 32053747 Review.
In incidentally detected PBMAH, hormonal evaluation includes testing for primary aldosteronism, pheochromocytoma and evaluation for autonomous cortisol secretion, using the 1 mg overnight dexamethasone suppression test. Midnight cortisol or 24-h urinary free cortisol may a …
In incidentally detected PBMAH, hormonal evaluation includes testing for primary aldosteronism, pheochromocytoma and evaluation for autonomo …
CT and MR imaging of the adrenal glands in ACTH-independent cushing syndrome.
Rockall AG, Babar SA, Sohaib SA, Isidori AM, Diaz-Cano S, Monson JP, Grossman AB, Reznek RH. Rockall AG, et al. Radiographics. 2004 Mar-Apr;24(2):435-52. doi: 10.1148/rg.242035092. Radiographics. 2004. PMID: 15026592 Review.
Bilateral disease--primary pigmented nodular adrenal dysplasia (PPNAD) (n = 2) and ACTH-independent macronodular adrenal hyperplasia (AIMAH) (n = 1)--had characteristic imaging features. ...
Bilateral disease--primary pigmented nodular adrenal dysplasia (PPNAD) (n = 2) and ACTH-independent macronodular adr …
Cushing's syndrome secondary to ACTH-independent macronodular adrenal hyperplasia.
Costa MH, Lacroix A. Costa MH, et al. Arq Bras Endocrinol Metabol. 2007 Nov;51(8):1226-37. doi: 10.1590/s0004-27302007000800008. Arq Bras Endocrinol Metabol. 2007. PMID: 18209860 Review.
ACTH-Independent macronodular adrenal hyperplasia (AIMAH) is a rare cause of endogenous Cushing's syndrome (CS), in which clinical features usually become apparent only after several decades of life. ...The diagnosis is suspected by bilateral ad …
ACTH-Independent macronodular adrenal hyperplasia (AIMAH) is a rare cause of endogenous Cushing's syndrom …
Familial vasopressin-sensitive ACTH-independent macronodular adrenal hyperplasia (VPs-AIMAH): clinical studies of three kindreds.
Gagliardi L, Hotu C, Casey G, Braund WJ, Ling KH, Dodd T, Manavis J, Devitt PG, Cutfield R, Rudzki Z, Scott HS, Torpy DJ. Gagliardi L, et al. Clin Endocrinol (Oxf). 2009 Jun;70(6):883-91. doi: 10.1111/j.1365-2265.2008.03471.x. Epub 2008 Nov 5. Clin Endocrinol (Oxf). 2009. PMID: 19018784
OBJECTIVE: Cushing's syndrome due to familial ACTH-independent macronodular adrenal hyperplasia (AIMAH) has been reported in small kindreds. ...MEASUREMENTS: Patients underwent clinical, biochemical and adrenal imaging investigations. Evaluation …
OBJECTIVE: Cushing's syndrome due to familial ACTH-independent macronodular adrenal hyperplasia (AIMAH) h …
Study of abnormal adrenal receptors in subjects with ACTH-independent Cushing's syndrome and nodular adrenal hyperplasia.
Ferri J, Perelló E, Lorente RI, Argente C, Rossetti P, Pedro T, Martinez-Hervas S, Real JT. Ferri J, et al. Endocrinol Diabetes Nutr (Engl Ed). 2020 Apr;67(4):245-252. doi: 10.1016/j.endinu.2019.07.005. Epub 2019 Oct 28. Endocrinol Diabetes Nutr (Engl Ed). 2020. PMID: 31672533 English, Spanish.
INTRODUCTION: ACTH-independent Cushing's Syndrome (AICS) accounts for 15-20% of cases of Cushing's syndrome, with <1% due to abnormal receptors. Our aim is to study the presence of abnormal receptors in subjects diagnosed with AICS with nodular adrenal hyperplasia in a …
INTRODUCTION: ACTH-independent Cushing's Syndrome (AICS) accounts for 15-20% of cases of Cushing's syndrome, with <1% due to abnor …
Clinical Spectrum of Adrenal Cushing's Syndrome and the Caution for Interpretation of Adrenocorticotrophic Hormone: A Single-Center Experience.
Gosavi V, Lila A, Memon SS, Sarathi V, Thakkar K, Dalvi A, Malhotra G, Prakash G, Patil V, Shah NS, Bandgar T. Gosavi V, et al. Horm Metab Res. 2022 Feb;54(2):57-66. doi: 10.1055/a-1735-3232. Epub 2022 Feb 7. Horm Metab Res. 2022. PMID: 35130566 Free article.
METHODS: Fifty-eight adrenal CS patients [Adrenocortical carcinoma (ACC), n=30; Adenoma (ACA), n=15; Primary pigmented nodular adrenocortical disease (PPNAD), n=10; ACTH independent macronodular adrenal hyperplasia (AIMAH), n=3) evaluated at a t …
METHODS: Fifty-eight adrenal CS patients [Adrenocortical carcinoma (ACC), n=30; Adenoma (ACA), n=15; Primary pigmented nodular adrenocortica …
Aberrant expression of multiple hormone receptors in ACTH-independent macronodular adrenal hyperplasia causing Cushing's syndrome.
de Groot JW, Links TP, Themmen AP, Looijenga LH, de Krijger RR, van Koetsveld PM, Hofland J, van den Berg G, Hofland LJ, Feelders RA. de Groot JW, et al. Eur J Endocrinol. 2010 Aug;163(2):293-9. doi: 10.1530/EJE-10-0058. Epub 2010 May 11. Eur J Endocrinol. 2010. PMID: 20460422
OBJECTIVE: Aberrant adrenal expression of various hormone receptors has been identified in ACTH-independent macronodular adrenal hyperplasia (AIMAH) causing cortisol hypersecretion regulated by hormones other than ACTH. ...LH/hCG-receptor (hCG-R …
OBJECTIVE: Aberrant adrenal expression of various hormone receptors has been identified in ACTH-independent macronodular …
ACTH-independent Cushing's syndrome due to ectopic endocrinologically functional adrenal tissue caused by a GNAS heterozygous mutation: a rare case of McCune-Albright syndrome accompanied by central amenorrhea and hypothyroidism: a case report and literature review.
Takedani K, Yamamoto M, Tanaka S, Ishihara S, Taketani T, Kanasaki K. Takedani K, et al. Front Endocrinol (Lausanne). 2022 Jul 25;13:934748. doi: 10.3389/fendo.2022.934748. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 35966069 Free PMC article. Review.
A 29-year-old woman was admitted to our hospital for fatigue and recent amenorrhea. Her plasma ACTH was <1.5 pg/mL, and her serum cortisol was 21.4 pg/mL after the 8 mg dexamethasone suppression test, revealing the presence of ACTH-independent Cushing's syndrome; howeve …
A 29-year-old woman was admitted to our hospital for fatigue and recent amenorrhea. Her plasma ACTH was <1.5 pg/mL, and her serum …
Macronodular adrenal hyperplasia due to mutations in an armadillo repeat containing 5 (ARMC5) gene: a clinical and genetic investigation.
Faucz FR, Zilbermint M, Lodish MB, Szarek E, Trivellin G, Sinaii N, Berthon A, Libé R, Assié G, Espiard S, Drougat L, Ragazzon B, Bertherat J, Stratakis CA. Faucz FR, et al. J Clin Endocrinol Metab. 2014 Jun;99(6):E1113-9. doi: 10.1210/jc.2013-4280. Epub 2014 Mar 6. J Clin Endocrinol Metab. 2014. PMID: 24601692 Free PMC article.
RESULTS: Germline ARMC5 mutations were found in 15 of 34 patients (44.1%). In silico analysis of the mutations indicated that seven (20.6%) predicted major implications for gene function. ...
RESULTS: Germline ARMC5 mutations were found in 15 of 34 patients (44.1%). In silico analysis of the mutations indicated that seven ( …
Corticotropin-independent macronodular adrenal hyperplasia: a clinicopathologic correlation.
Swain JM, Grant CS, Schlinkert RT, Thompson GB, vanHeerden JA, Lloyd RV, Young WF. Swain JM, et al. Arch Surg. 1998 May;133(5):541-5; discussion 545-6. doi: 10.1001/archsurg.133.5.541. Arch Surg. 1998. PMID: 9605918
OBJECTIVES: To investigate the clinical presentation, laboratory findings, and pathologic characteristics of patients with corticotropin (ACTH)-independent macronodular adrenal hyperplasia. DESIGN: Retrospective review. ...No patient had elevate …
OBJECTIVES: To investigate the clinical presentation, laboratory findings, and pathologic characteristics of patients with corticotropin ( …
27 results