Cargando…

SAT-LB38 Clinical Features, Treatment and Prognosis of Primary Bilateral Macronodular Adrenal Hyperplasia Compared With Unilateral Adrenal Cortisol-Secreting Adenoma: Analysis of 46 Chinese Cases

Objectives: Primary bilateral macronodular adrenal hyperplasia (PBMAH) is a rare condition of Cushing’s syndrome (CS) characterized by benign bilateral enlarged adrenal masses. The aim of this study is to analyze clinical features, individualized treatment and prognosis of PBMAH. Methods: Clinical d...

Descripción completa

Detalles Bibliográficos
Autores principales:	Zhang, Qian, Xiao, Haiying, Gu, Weijun
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Oxford University Press 2020
Materias:	Adrenal
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7207973/ http://dx.doi.org/10.1210/jendso/bvaa046.2039

Ejemplares similares

SUN-390 A Rare Case of Bilateral Macronodular Adrenal Hyperplasia Discovered Incidentally
por: Penaherrera, Carlos, 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)

ODP018 A Case of Cushing's Syndrome due to Primary Bilateral Macronodular Adrenal Hyperplasia
por: Veluru, Manasa, et al.
Publicado: (2022)

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)

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

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

MON-209 Identification of a New Heterozygous Germline ARMC5 Deletion in a Familial Case of Primary Bilateral Macronodular Adrenal Hyperplasia Co-Secreting Cortisol and Aldosterone
por: Salle, Stefanie Parisien-La, et al.
Publicado: (2020)

Epinephrine to the Rescue: Identifying the Offending Side in Bilateral (B/L) Macronodular Adrenal Hyperplasia (BMAH) With Cushing Syndrome (CS) and Hyperaldosteronism
por: Vedere, Tarunya, et al.
Publicado: (2021)

SAT-LB42 Bilateral Large Calcified Adrenal Leiomyoma Mimicking Adrenal Malignancy: A Rare Case Report With Literature Review
por: Jajah, Mohammad Bilal M, et al.
Publicado: (2020)

SAT-371 Correlation of Midnight and Post Dexamethasone Salivary Cortisone and Cortisol with Post Dexamethasone Serum Cortisol Concentrations In Patients with Unilateral and Bilateral Adrenal Incidentalomas
por: Naseem, Asma, et al.
Publicado: (2019)

SAT-LB067 Mutational Spectrum Determines Subtle Adrenal Biosynthetic Defect in Non-Classical Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
por: Mermejo, Livia, et al.
Publicado: (2019)

SAT-LB37 Frailty in Patients With Mild Autonomous Cortisol Secretion Is Higher Than Patients With Nonfunctioning Adrenal Tumors
por: singh, sumitabh, et al.
Publicado: (2020)

Large Bilateral Adrenal Myelolipomas in the Setting of Congenital Adrenal Hyperplasia
por: Anderson, Karolina E, et al.
Publicado: (2021)

FRI220 Primary Bilateral Macronodular Adrenal Hyperplasia: A Rare Cause Of Cushing Syndrome
por: Ortiz, Yineli, et al.
Publicado: (2023)

An Unusual Case of Bilateral Adrenal Hyperplasia
por: De Castro, Alicia, et al.
Publicado: (2021)

SAT-LB41 Surgery Outcomes for Patients With Primary Aldosteronism Who Show Normal-Appearing Adrenals on Computed Tomography but Unilateral Disease on Adrenal Venous Sampling
por: Aono, Daisuke, et al.
Publicado: (2020)

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)

Retention of aberrant cortisol secretion in a patient with bilateral macronodular adrenal hyperplasia after unilateral adrenalectomy
por: Tanaka, Sho, et al.
Publicado: (2019)

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

SAT-207 Adrenocortical Carcinoma in Untreated Congenital Adrenal Hyperplasia
por: David, Julia, et al.
Publicado: (2020)

Hypertension with unilateral adrenal aldosterone and cortisol cosecreting adenoma: A case report
por: Hu, Zhe, et al.
Publicado: (2021)

OR04-4 Loss of KDM1A in Bilateral Macronodular Adrenal Hyperplasia With GIP-Dependent Cushing's Syndrome and in Acromegaly With Paradoxical GH Response to Oral Glucose
por: Amazit, Larbi, et al.
Publicado: (2022)

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)

MON-LB043 A Case of Renovascular Hypertension With Cortisol-Producing Adrenal Masses
por: Higashitani, Takuya, et al.
Publicado: (2020)

SAT-193 Clinical Case of ARMC5 Tumor Syndrome: A Rare Case of Cushing’s Syndrome from Primary Bilateral Macronodular Adrenal Hyperplasia Caused by ARMC5 Mutation with Concomitant Presence of Meningiomas and Primary Hyperparathyroidism
por: Parikh, Sahil, et al.
Publicado: (2020)

SAT-372 Correlation of Serum Dexamethasone and Cortisol Concentrations Post Dexamethasone 1 Mg in the Overnight Dexamethasone Suppression Test in Patients with Unilateral and Bilateral Adrenal Incidentalomas
por: Naseem, Asma, et al.
Publicado: (2019)

SAT330 Recurrence of Acth Independent Cushing Syndrome In Patient With Previously Operated On For Primary Bilateral Macronodular Adrenal Hyperplasia And Co-existence Of Papillary Thyroid Carcinoma
por: Vashakmadze, Natia, et al.
Publicado: (2023)

SAT-377 Characteristics of Reproductive Age Women with Incidental Adrenal Adenomas
por: Sokoloff, Samatha, et al.
Publicado: (2019)

SUN-372 A Case of Adrenal Adenoma Co-Secreting Aldosterone and Cortisol: Limits of Adrenal Vein Sampling
por: Reddy, Ramadurgam Poliki Monica, et al.
Publicado: (2019)

SUN-382 Heterogeneous Clinical Presentation In Familial Cases Of Primary Macronodular Adrenal Hyperplasia (PMAH): The Influence Of Somatic Event Of ARMC5.
por: Brondani, Vânia, et al.
Publicado: (2019)

Bilateral Adrenal Adenomas Attributed to Extrapulmonary Mycobacterium Tuberculosis
por: Elmaaz, Ahmed, et al.
Publicado: (2021)

SAT-LB062 Adrenal Sexual Dimorphism Is Abolished by Tissue-Targeted Deletion of the Androgen Receptor
por: Frucci, Emily, et al.
Publicado: (2019)

SAT-182 Bilateral Adrenal Hemorrhage with Clinically Preserved Adrenal Function Leading to the Diagnosis of Antiphospholipid Syndrome
por: Hurtado, Carolina, et al.
Publicado: (2020)

SUN-LB38 Adrenal Tumor Causing Unexplained Hyperhidrosis in a Young Man
por: Unterborn, Rebecca, et al.
Publicado: (2020)

SAT-190 Are Pet Scans Needed in Evaluating Lipid Rich Adrenal Adenomas?
por: Castellanos-Diaz, Jessica, et al.
Publicado: (2020)

Surgically Treated Resistant Hypertension Due to Bilateral Adrenal Hyperplasia
por: Ganesan, Kavitha, et al.
Publicado: (2021)

SAT-184 Silent Pheochromocytoma Complicated by Adrenal Insufficiency After Unilateral Adrenalectomy
por: Aftab, Hassaan B, et al.
Publicado: (2020)

FRI266 Medical Management Of Cushing’s Syndrome Caused By Primary Bilateral Macronodular Adrenal Hyperplasia (PBMA) With Low Dose Of Ketoconazole
por: Hatfield, Jennifer S, et al.
Publicado: (2023)

PSAT019 A Rare Case of Massive Bilateral Adrenal Myelolipomas in a Patient with Congenital Adrenal Hyperplasia
por: Arasu, Aarthi, et al.
Publicado: (2022)

SAT-LB066 Clinical Characteristics of Incidentally Discovered Functioning Adrenal Tumors: Study of Advancing Care and Pathogenesis of Intractable Adrenal Diseases in Japan (ACPA-J)
por: Tanabe, Akiyo, et al.
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_b1sa5kr674ufkrpuptpdrt6845