Cargando…

The role of adrenal venous sampling (AVS) in primary bilateral macronodular adrenocortical hyperplasia (PBMAH): a study of 16 patients

OBJECTIVE: Primary bilateral macronodular adrenocortical hyperplasia (PBMAH) is a rare cause of ACTH-independent Cushing’s syndrome. Current guidelines recommend bilateral adrenalectomy for PBMAH, but several studies showed clinical effectiveness of unilateral adrenalectomy despite bilateral disease...

Descripción completa

Detalles Bibliográficos
Autores principales:	Rubinstein, German, Osswald, Andrea, Braun, Leah Theresa, Vogel, Frederick, Kroiss, Matthias, Pilz, Stefan, Deniz, Sinan, Aigner, Laura, Knösel, Thomas, Bertherat, Jérôme, Bouys, Lucas, Ladurner, Roland, Riester, Anna, Bidlingmaier, Martin, Beuschlein, Felix, Reincke, Martin
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Springer US 2022
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9068666/ https://www.ncbi.nlm.nih.gov/pubmed/35274284 http://dx.doi.org/10.1007/s12020-022-03020-z

Ejemplares similares

Steroid profiling using liquid chromatography mass spectrometry during adrenal vein sampling in patients with primary bilateral macronodular adrenocortical hyperplasia
por: Zhang, Ru, et al.
Publicado: (2022)

Primary bilateral macronodular adrenocortical hyperplasia (PBMAH) patient with ARMC5 mutations
por: Tang, Peng, et al.
Publicado: (2023)

ARMC5 mutation in a Portuguese family with primary bilateral macronodular adrenal hyperplasia (PBMAH)
por: Rego, Teresa, et al.
Publicado: (2017)

New pathogenic variants in ARMC5 gene in a series of Italian patients affected by primary bilateral macronodular adrenocortical hyperplasia (PBMAH)
por: Giacché, Mara, et al.
Publicado: (2023)

OR02-6 Mass Spectrometry-Based Steroid Profiling Inprimary Bilateral Macronodular Adrenocortical Hyperplasia
por: Hannah-Shmouni, Fady, et al.
Publicado: (2019)

Intermittent Blurry Vision: An Unexpected Presentation of Cushing’s Syndrome Due to Primary Bilateral Macronodular Adrenal Hyperplasia (PBMAH)
por: Fernandez, Christopher, et al.
Publicado: (2022)

OR08-01 Expression of Gonadal Differentiation Markers in Bilateral Macronodular Adrenocortical Disease
por: De Sousa, Kelly, et al.
Publicado: (2023)

Toward a Diagnostic Score in Cushing's Syndrome
por: Braun, Leah T., et al.
Publicado: (2019)

THU623 Leuprolide Treatment Of Mild Cortisol Secretion (MACS) Due To Primary Bilateral Macronodular Hyperplasia (PBMAH) Expressing Aberrant LH Receptors
por: Branchaud-Croisetière, Laurie, et al.
Publicado: (2023)

A case of renovascular hypertension with incidental primary bilateral macronodular adrenocortical hyperplasia
por: Higashitani, Takuya, et al.
Publicado: (2020)

Cell-To-Cell Communication in Bilateral Macronodular Adrenal Hyperplasia Causing Hypercortisolism
por: Lefebvre, Hervé, et al.
Publicado: (2015)

A case of Adrenocoricotrophic hormone -independent bilateral adrenocortical macronodular hyperplasia concomitant with primary aldosteronism
por: Tokumoto, Mao, et al.
Publicado: (2017)

A novel nonsense mutation in ARMC5 causes primary bilateral macronodular adrenocortical hyperplasia
por: He, Wen-Tao, et al.
Publicado: (2021)

OR12-3 Identification of Predictive Criteria for the Primary Bilateral Macronodular Adrenal Hyperplasia Gene ARMC5: A European Series of 352 Unselected Patients.
por: Assié, Guillaume, et al.
Publicado: (2022)

Targeting heterogeneity of adrenocortical carcinoma: Evaluation and extension of preclinical tumor models to improve clinical translation
por: Hantel, Constanze, et al.
Publicado: (2016)

Diagnosis and treatment of adrenocorticotrophic hormone-independent macronodular adrenocortical hyperplasia: A report of 23 cases in a single center
por: LI, JIANG, et al.
Publicado: (2015)

Analysis of clinical and pathological features of primary bilateral macronodular adrenocortical hyperplasia compared with unilateral cortisol-secreting adrenal adenoma
por: Zhang, Qian, et al.
Publicado: (2020)

Heterogeneous circulating miRNA profiles of PBMAH
por: Hara, Kazunari, et al.
Publicado: (2022)

Circulating microRNA Expression in Cushing’s Syndrome
por: Vetrivel, Sharmilee, et al.
Publicado: (2021)

OR04-3 Genetic Alterations of ARMC5 and KDM1A Are Associated With Different Expression Profiles of Illegitimate Receptors in Primary Bilateral Macronodular Adrenal Hyperplasia
por: Armignacco, Roberta, et al.
Publicado: (2022)

Macronodular adrenal hyperplasia masquerading as an upper pole renal mass
por: Owens-Walton, Jeunice, et al.
Publicado: (2021)

SUN-354 Quality of Life in Patients with Primary Macronodular Adrenal Hyperplasia
por: Charchar, Helaine, et al.
Publicado: (2019)

A New Insight into the Surgical Treatment of Primary Macronodular Adrenal Hyperplasia
por: Yoshiaki Tanno, Fabio, et al.
Publicado: (2020)

The effect of unilateral adrenalectomy on patients with primary bilateral macronodular adrenal hyperplasia
por: Yu, Zhongwei, et al.
Publicado: (2023)

Persisting Muscle Dysfunction in Cushing’s Syndrome Despite Biochemical Remission
por: Vogel, Frederick, et al.
Publicado: (2020)

Long-term low-dose ketoconazole treatment in bilateral macronodular adrenal hyperplasia
por: Comte-Perret, Sophie, et al.
Publicado: (2014)

Maffucci Syndrome Associated With Adrenocorticotropic Hormone–Independent Bilateral Macronodular Adrenal Hyperplasia
por: Tricò, Domenico, et al.
Publicado: (2017)

ARMC5 mutations in familial and sporadic primary bilateral macronodular adrenal hyperplasia
por: Yu, Liping, et al.
Publicado: (2018)

Inhibin A as a tumor marker for primary bilateral macronodular adrenal hyperplasia
por: Wurth, Rachel, et al.
Publicado: (2020)

Mifepristone Treatment in Four Cases of Primary Bilateral Macronodular Adrenal Hyperplasia (BMAH)
por: Cohan, Pejman, et al.
Publicado: (2019)

Primary Macronodular Adrenal Hyperplasia Associated With Autosomal Dominant ARMC5 Mutation
por: Kerut, Sarah Elizabeth, et al.
Publicado: (2021)

Metformin and Bone Metabolism in Endogenous Glucocorticoid Excess: An Exploratory Study
por: Vogel, Frederick, et al.
Publicado: (2021)

Adrenocorticotropic hormone-independent macronodular adrenal hyperplasia with abnormal cortisol secretion mediated by catecholamines
por: Rhee, Harin, et al.
Publicado: (2014)

SUN-390 A Rare Case of Bilateral Macronodular Adrenal Hyperplasia Discovered Incidentally
por: Penaherrera, Carlos, et al.
Publicado: (2019)

Coexistence of Myelolipoma and Primary Bilateral Macronodular Adrenal Hyperplasia With GIP-Dependent Cushing's Syndrome
por: Larose, Stéphanie, et al.
Publicado: (2019)

Unlikely Coexistence of Sporadic Pheochromocytoma and Bilateral Macronodular Adrenal Hyperplasia: A Challenge to Manage
por: Dinh, Kathryn, et al.
Publicado: (2021)

Epithelial and Mesenchymal Markers in Adrenocortical Tissues: How Mesenchymal Are Adrenocortical Tissues?
por: Sbiera, Iuliu, et al.
Publicado: (2021)

Macronodular hepatosplenic tuberculosis
por: Guidi, Roberto, et al.
Publicado: (2012)

ACTH-independent macronodular adrenocortical hyperplasia reveals prevalent aberrant in vivo and in vitro responses to hormonal stimuli and coupling of arginine-vasopressin type 1a receptor to 11β-hydroxylase
por: Hofland, Johannes, et al.
Publicado: (2013)

ARMC5 Alterations in Primary Macronodular Adrenal Hyperplasia (PMAH) and the Clinical State of Variant Carriers
por: Kyo, Chika, et al.
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_n9k3c13qtrelcinscltks468gn