Cargando…

Primary malignant tumors of the adrenal glands

Malignancy must be considered in the management of adrenal lesions, including those incidentally identified on imaging studies. Adrenocortical carcinomas (ACCs) are rare tumors with an estimated annual incidence of 0.7–2 cases per year and a worldwide prevalence of 4–12 cases per million/year. Howev...

Descripción completa

Detalles Bibliográficos
Autores principales:	Almeida, Madson Q, Bezerra-Neto, Joao Evangelista, Mendonça, Berenice B, Latronico, Ana Claudia, Fragoso, Maria Candida B V
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo 2018
Materias:	Review Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257058/ https://www.ncbi.nlm.nih.gov/pubmed/30540124 http://dx.doi.org/10.6061/clinics/2018/e756s

Ejemplares similares

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)

Adrenal Insufficiency and Glucocorticoid Use During the COVID-19 Pandemic
por: Almeida, Madson Q., et al.
Publicado: (2020)

FRI193 Early Presentation Of Pediatric Oncocytic Adrenal Tumor Associated With Germline TP53 Pathogenic Variant—Report Of Three Cases
por: Oppenheimer, Romulo R V, et al.
Publicado: (2023)

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-070 Clinical and Imaging Characteristics of Primary Unilateral Adrenal Hyperplasia in Primary Aldosteronism
por: Rassi-Cruz, Marcela, et al.
Publicado: (2019)

SAT-560 Usefulness of Contralateral Suppression in Adrenal Venous Sampling to Define Lateralization in Primary Aldosteronism
por: Freitas, Thaís C, et al.
Publicado: (2020)

FRI256 The Clinical Impacts Of Bi-allelic Germline Pathogenic Variant In TP53 In Two Patients With Li-Fraumeni Syndrome
por: Petry, Vanessa, et al.
Publicado: (2023)

Amplification of the Insulin-Like Growth Factor 1 Receptor Gene Is a Rare Event in Adrenocortical Adenocarcinomas: Searching for Potential Mechanisms of Overexpression
por: Ribeiro, Tamaya Castro, et al.
Publicado: (2014)

MicroRNA Era: The Importance for Diagnosis and Prognosis of Adrenocortical Tumors
por: Bezerra, João Evangelista, et al.
Publicado: (2014)

MON-202 Germline SDHB Exon 1 Deletion Is Associated with Absence of (131)I-metaiodobenzylguanidine (MIBG) Uptake in Malignant Paragangliomas
por: Petenuci, Janaina, et al.
Publicado: (2020)

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

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

Genetic Diagnosis of Primary Adrenal Insufficiency in Children: A Paradigm Change
por: Almeida, Madson Q
Publicado: (2021)

Retrospective Analysis of Prognostic Factors in Pediatric Patients with Adrenocortical Tumor from Unique Tertiary Center with Long-Term Follow-Up
por: Bachega, Fernanda S., et al.
Publicado: (2022)

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)

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)

Familial Adenomatous Polyposis Associated With Bilateral Adrenocortical Tumors and Agressive Desmoid Tumor
por: Neiva, Raíssa P, et al.
Publicado: (2021)

Low Protein Expression of both ATRX and ZNRF3 as Novel Negative Prognostic Markers of Adult Adrenocortical Carcinoma
por: Brondani, Vania Balderrama, et al.
Publicado: (2021)

Adjuvant radiotherapy for the primary treatment of adrenocortical carcinoma: are we offering the best?
por: Srougi, Victor, et al.
Publicado: (2017)

SAT-320 A Synonymous Pathogenic Variant (p.l180=) in SDHB Gene Identified in a Young Patient with Abdominal Paraganglioma
por: Petenuci, Janaina, et al.
Publicado: (2019)

Low DICER1 expression is associated with poor clinical outcome in adrenocortical carcinoma
por: de Sousa, Gabriela Resende Vieira, et al.
Publicado: (2015)

THU587 High Prevalence Of Primary Aldosteronism Diagnosis In Patients With Papillary Thyroid Cancer And Hypertension: A Cross-sectional Case-control Study
por: Ana Wolf, Ana Alice Wolf Maciel, et al.
Publicado: (2023)

FRI143 Serum Aldosterone Levels Predict Decline In Renal Function After Unilateral Adrenalectomy For Primary Aldosteronism
por: Stumpf, Matheo A M, et al.
Publicado: (2023)

FRI267 Carney Complex From A Single Familycarney Complex From A Single Family Followed Up Over 20 Years With Different Clinical Pattern Evolution
por: Kuhn, Aliny W, et al.
Publicado: (2023)

SAT322 Case report: Impact Of Combined Treatment To Prolong Overall Survival In Advanced Adrenocortical Pediatric Cancer Associated With Li-Fraumeni Syndrome
por: de Magalhães, Isabelle P A, et al.
Publicado: (2023)

Allelic Variants of ARMC5 in Patients With Adrenal Incidentalomas and in Patients With Cushing's Syndrome Associated With Bilateral Adrenal Nodules
por: Mariani, Beatriz Marinho de Paula, et al.
Publicado: (2020)

Incidence of adrenal gland tumor as a second primary malignancy: SEER-based study
por: Rashed, Wafaa M, et al.
Publicado: (2018)

SUN-178 Clinical and Anatomopathological Characteristics of Two Atypical Aldosterone-Producing Adenomas
por: Goldbaum, Tatiana Silva, et al.
Publicado: (2020)

SUN-195 Bilateral Aldosterone-Producing Adenomas: A New Subtype of Bilateral Primary Aldosteronism?
por: Maciel, Ana Alice Wolf, et al.
Publicado: (2020)

Editorial: Molecular -genetic causes underlying primary adrenal insufficiency: Current insights into diagnosis and treatment
por: Fragoso, Maria Candida B.V., et al.
Publicado: (2022)

Adrenal crisis and mortality rate in adrenal insufficiency and congenital adrenal hyperplasia
por: Lousada, Lia Mesquita, et al.
Publicado: (2021)

Long-term Results after CT-Guided Percutaneous Ethanol Ablation for the Treatment of Hyperfunctioning Adrenal Disorders
por: Frenk, Nathan Elie, et al.
Publicado: (2016)

OR29-3 Targeted Assessment of G0S2 Methylation Identifies a Rapidly Recurrent, Routinely Fatal Molecular Subtype of Adrenocortical Carcinoma
por: Mohan, Dipika, et al.
Publicado: (2019)

SAT307 Intraoperative Radiofrequency Ablation Of An Unresectable Abdominal Paraganglioma Promoted Objective Tumor Response And Complete Biochemical Remission
por: de Magalhães, Isabelle P A, et al.
Publicado: (2023)

RF21 | PSAT76 Epigenetic Programs Stabilize a Differentiated Cell State Required for Sustained Proliferation in Adrenocortical Carcinoma
por: Mohan, Dipika, et al.
Publicado: (2022)

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)

Glucose-dependent insulinotropic peptide receptor overexpression in adrenocortical hyperplasia in MEN1 syndrome without loss of heterozygosity at the 11q13 locus
por: Costa, Marcia Helena Soares, et al.
Publicado: (2011)

Tumors of the adrenal gland and extra-adrenal paraganglia
por: Lack, Ernest E.
Publicado: (1997)

Oncocytic Tumors: An Uncommon Benign Adrenal Gland Lesions With Features of Malignancy
por: Elazime, Zineb, et al.
Publicado: (2023)

Primary Leiomyosarcoma of the Adrenal Gland
por: Etten, Boudewijn van, et al.
Publicado: (2001)

Cannot write session to /tmp/vufind_sessions/sess_d7u070ttqg16rl1ksd7hcnpq64