Cargando…

SUN-354 Quality of Life in Patients with Primary Macronodular Adrenal Hyperplasia

Background: The majority of patients with Cushing’s syndrome (CS) have physical and psychological symptoms that may lead to impaired quality of life (QoL). QoL improving with treatment but remaining significantly impaired compared with the general population despite long-term remission. Aim of this...

Descripción completa

Detalles Bibliográficos
Autores principales:	Charchar, Helaine, Brondani, Vânia, Ferreira, Amanda, Campanholo, Kenia, Ribeiro, Elyse, Fragoso, Maria, Verduguez, Elisa
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Endocrine Society 2019
Materias:	Adrenal
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6553354/ http://dx.doi.org/10.1210/js.2019-SUN-354

Ejemplares similares

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)

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

SUN-351 Are We Underestimating The Role Of Systemic Chemotherapy In The Treatment Of Localized And Advanced Adrenocortical Carcinoma?
por: Ferreira, Amanda, et al.
Publicado: (2019)

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

SUN-180 A Case of Deoxycorticosterone-Producing Malignant Adrenocortical Tumor
por: Cartolano, Natasha Scaranello, et al.
Publicado: (2020)

An Overview of the Heterogeneous Causes of Cushing Syndrome Resulting From Primary Macronodular Adrenal Hyperplasia (PMAH)
por: Charchar, Helaine Laiz Silva, et al.
Publicado: (2022)

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)

A New Insight into the Surgical Treatment of Primary Macronodular Adrenal Hyperplasia
por: Yoshiaki Tanno, Fabio, 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)

MON-206 Diagnosis of Non-Functional Masses in Adrenal Gland Topography - Experience of a Tertiary Health Center
por: Brondani, Vânia Balderrama, et al.
Publicado: (2020)

SAT-178 Incidence, Patterns of Clinical Presentation, and Outcomes of Patients with Brain Metastasis Due to Adrenocortical Carcinoma
por: Amorim, Larissa Costa, et al.
Publicado: (2020)

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
por: Zhang, Qian, 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)

SUN-374 Management of Congenital Adrenal Hyperplasia in Pregnancy with Female Fetus
por: Kothari, Vallari, et al.
Publicado: (2019)

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)

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

SUN-361 Reproductive Outcomes in Females with Virilizing Forms of Congenital Adrenal Hyperplasia
por: Falcao, Camila, et al.
Publicado: (2019)

SUN-174 Giant Bilateral Myelolipomas in a Patient with Congenital Adrenal Hyperplasia
por: Duro, Teodor, et al.
Publicado: (2020)

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

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)

SUN-172 A False Positive Result in Newborn Screening for Congenital Adrenal Hyperplasia (CAH) in a Girl with Beckwith Wiedemann Syndrome
por: Braga, Barbara Leitao, et al.
Publicado: (2020)

SUN-197 Giant Adrenal Myelolipoma Associated with Prolonged ACTH Elevation in a Patient with Congenital Adrenal Hyperplasia (CAH)
por: Kaluarachchi, Vidumini, et al.
Publicado: (2020)

SUN-173 A Gigantic Uterine Leiomyoma and Big Bilateral Adrenal Myelolipomas as a Result of Untreated Congenital Adrenal Hyperplasia
por: La, Betty, et al.
Publicado: (2020)

SUN-371 Successful Induction of Fertility with Low-Dose Dexamethasone in a Patient with Congenital Adrenal Hyperplasia and Testicular Adrenal Rest Tumor
por: Jha, Smita, et al.
Publicado: (2019)

SUN-167 Treatment Considerations for a Healthy Pregnancy in Women with Classical Congenital Adrenal Hyperplasia (CAH)
por: Calzia, Megan, et al.
Publicado: (2020)

ODP144 Cushing Syndrome and Primary Hyperaldosteronism due to Synchronic Bilateral Adrenal Adenomas with Exclusive Production of Cortisol on the Right and Aldosterone on the Left
por: Rolim, Marina Rocha, et al.
Publicado: (2022)

SUN-398 A Case of Bilateral Testicular Adrenal Rest Tumors in a Patient with Congenital Adrenal Hyperplasia Due to 21 Hydroxylase Deficiency
por: Alsaeed, Abdulghani
Publicado: (2019)

SUN-218 Analysis of ATRX and ZNRF3 Expression and Copy Number Variation in a Pediatric and Adult Cohort with Adrenocortical Tumors
por: Brondani, Vânia Balderrama, et al.
Publicado: (2020)

SUN-170 Adrenal Insufficiency Due to Adrenal Hemorrhage
por: Bansal, Rashika, et al.
Publicado: (2020)

SUN-358 Dual Release Hydrocortisone as a New Treatment for Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
por: Simeoli, Chiara, et al.
Publicado: (2019)

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)

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)

SUN-183 Adrenalitis Induced by Nivolumab
por: Khan, Muhammad Atique Alam, et al.
Publicado: (2020)

SAT-165 Sterol O-Acyl Transferase 1 as a Prognostic Marker of Adrenocortical Carcinoma
por: Lacombe, Amanda Meneses Ferreira, et al.
Publicado: (2020)

SUN-206 A Rare Case of Untreated Congenital Adrenal Hyperplasia Leading to Gender Dysphoria and a Female to Male Transgender
por: Awad, Dana, et al.
Publicado: (2020)

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

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

SUN-164 Adrenal Crisis in Early Pregnancy
por: Bello, Jenny Carolina, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_ru3j3nv81hn2anjoemeilkdn0c