Cargando…

Recurrent Pheochromocytoma, as Component of Multiple Endocrine Neoplasia

Background: Pheochromocytoma is a rare neuroendocrine tumor from the adrenal medulla’s chromaffin cells that secrete catecholamines. The mainstay of treatment is surgery. Although rare, it has a recurrence rate of 6.5-16.5% even after adequate surgical removal with a notable increase in prevalence a...

Descripción completa

Detalles Bibliográficos
Autores principales:	Dominguez, Hydelene Beray, Pacheco, Elizabeth P, Jimeno, Cecilia, Lantion-Ang, Franceslina C, Hernandez, Edrome, Chiu, Harold Henrison Chang
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Oxford University Press 2021
Materias:	Tumor Biology
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8089295/ http://dx.doi.org/10.1210/jendso/bvab048.2055

Ejemplares similares

A Rare Presentation of Multiple Endocrine Neoplasia Type 1
por: Pradeep, Pallavi, et al.
Publicado: (2021)

SAT-LB310 A Mysterious Multiple Endocrine Neoplasia (MEN) Like Syndrome
por: Soe, Myat Han, et al.
Publicado: (2020)

MON-906 MULTIPLE ENDOCRINE NEOPLASIA TYPE 2A: Familiar Case Report
por: Sousa, Barbara K P, et al.
Publicado: (2020)

MON-922 Multiple Endocrine Neoplasia Type 1- A Clarion Call for Clarity
por: Hashmi, Hiba, et al.
Publicado: (2020)

Thymoma and Not Just Thymic Carcinoid Can Be Associated With Multiple Endocrine Neoplasia Type 1
por: Graf, Akua, et al.
Publicado: (2021)

SUN-912 The Rare Men of Mississippi Complications in the Diagnosis of Multiple Endocrine Neoplasia Type 1
por: Rashid, Hytham, et al.
Publicado: (2020)

ODP538 A Case of Multiple Endocrine Neoplasia Type 2A with Malignant Paraganglioma
por: Ozawa, Atsushi, et al.
Publicado: (2022)

Calvarial metastasis from malignant pheochromocytoma associated with multiple endocrine neoplasia
por: Hernandez, Mary Angeline Luz Ubias, et al.
Publicado: (2022)

Papillary Thyroid Carcinoma and Cushing’s Disease: A Rare Association With Multiple Endocrine Neoplasia Type 1
por: Benevides, Léo Nunes, et al.
Publicado: (2021)

RF07 | PSUN366 An Uncommon Path Leading to Diagnosis of Multiple Endocrine Neoplasia 2A
por: Gokul, Sagarika, et al.
Publicado: (2022)

MON-321 Metastatic Melanoma with Unknown Primary Site in a Patient with Multiple Endocrine Neoplasia Type 1
por: Kamilaris, Crystal, et al.
Publicado: (2019)

SAT-LB060 Clinical Presentation and Management of Primary Ovarian Carcinoids in Multiple Endocrine Neoplasia Type 1
por: Jhawar, Sakshi, et al.
Publicado: (2019)

SUN-940 Carney Complex: A Case of a Rare Multiple Endocrine Neoplasia Misdiagnosed as Peutz-Jeghers Syndrome
por: Vaid, Sonal, et al.
Publicado: (2020)

THU522 Symptomatic Hypoglycemia As The First Manifestation Of Multiple Endocrine Neoplasia Type 1 (MEN-1): Case Report
por: Oliveira, Vitória Dupas, et al.
Publicado: (2023)

SAT-317 The Importance of Accurate Genetic Diagnosis Highlighted in a Case of Recurrent Bilateral Pheochromocytomas
por: Choo, Kuan Swen, et al.
Publicado: (2019)

Local recurrence of pheochromocytoma in multiple endocrine neoplasia type 2A: a diagnostic and therapeutic challenge
por: Tramunt, Blandine, et al.
Publicado: (2016)

RF05 | PSUN364 A Rare Case of Bilateral Parathyroid Carcinoma in the Setting of Multiple Endocrine Neoplasia Type 1
por: Kesavan Chary, Priyanka, et al.
Publicado: (2022)

Multiple Endocrine Neoplasia 2a Presenting with Pheochromocytoma and Pituitary Macroadenoma
por: Heinlen, Jonathan E., et al.
Publicado: (2011)

Hypercalcemia in Pheochromocytoma: From MEN to VHL
por: Mittal, Madhukar, et al.
Publicado: (2021)

SAT-324 An Unusual Association between Pheochromocytoma and Hyperparathyroidism in a Patient with Neurofibromatosis Type 1: A Possible Co-Occurrence of Two Hereditary Endocrine Tumor Syndromes
por: Kiatpanabhikul, Phatharaporn, et al.
Publicado: (2019)

A Blood-Based Polyamine Signature Associated With Disease Progression in Patients With Multiple Endocrine Neoplasia Type 1-Related Duodenopancreatic Neuroendocrine Tumors
por: Fahrmann, Johannes F, et al.
Publicado: (2021)

RF27 | LBSUN362 Germline CDKN1B Variants Type And Site Are Associated With Specific Phenotype In Multiple Endocrine Neoplasia 4
por: Halperin, Reut, et al.
Publicado: (2022)

SUN-128 Impaired Fasting Glucose Is Associated with Insulin Resistance in Patients with Germline Mutations in the Multiple Endocrine Neoplasia Type 1 (MEN1) Gene
por: Bansal, Rashika, et al.
Publicado: (2020)

Concomitant existence of pheochromocytoma in a patient with multiple endocrine neoplasia type 1
por: Okada, Ryo, et al.
Publicado: (2016)

SUN-939 Case Report: Malignant Pheochromocytoma
por: Lima, Jose Viana, et al.
Publicado: (2020)

MON-915 Acute Abdominal Pain and the Pheochromocytoma
por: Weiner, Yotam, et al.
Publicado: (2020)

Composite Pheochromocytoma With Ganglioneuroblastoma: A Case Report
por: Pastor, Paola M Lockhart, et al.
Publicado: (2021)

MON-335 Phenocopy of Multiple Endocrine Neoplasia Type 1 (MEN1) Due to a Germline Cell Division Cycle 73 (CDC73) Variant
por: Lines, Kate, et al.
Publicado: (2019)

SUN-938 Rare Case of Ectopic Cushing Syndrome Caused by ACTH Secreting Thymic Neuroendocrine Tumor in a Patient with Multiple Endocrine Neoplasia Type 1
por: Gorantla, Yamuna, et al.
Publicado: (2020)

SUN-902 Bradycardia as a Presentation of Malignant Pheochromocytoma
por: Saleem, Marwa, et al.
Publicado: (2020)

An Exploration of Knowledge and Themes on Diabetes during Outpatient Consultation in a Tertiary Referral Hospital*
por: Uy, Angelique Bea, et al.
Publicado: (2021)

Weekly Versus Daily Levothyroxine Tablet Replacement in Adults with Hypothyroidism: A Meta-Analysis
por: Chiu, Harold Henrison, et al.
Publicado: (2021)

SAT-313 Catecholamine-Induced Cardiomyopathy in Pheochromocytoma during Pregnancy
por: Barreiro, Margarita, et al.
Publicado: (2019)

Clinical Activity of Selpercatinib in RET Mutant Pheochromocytoma-Case Reports
por: Konda, Bhavana, et al.
Publicado: (2021)

SUN-909 A Unique Presentation of Multiple Endocrine Neoplasia (MEN) Type 1 Mosaicism Caused by a Novel c.124G>A Variant in the MEN1 Gene
por: Drummond, Russell Sinclair, et al.
Publicado: (2020)

Comparative Analysis of Different International Criteria (ACMG-AMP vs. TENGEN) Applied to Classification of Missense Germline Allelic Variants in Patients With Multiple Endocrine Neoplasia Type 1 or Suspected to this Syndrome
por: Lugeiro, Palloma C, et al.
Publicado: (2021)

Comprehensive Analysis of Clinical Features in Index Cases With Multiple Endocrine Neoplasia Type 1 Refine the Risk Rate for Detection of Mutation Distinguishing Negative-Mutation (Phenocopies) and Positive-Mutation Cases
por: Urtremari, Betsaida, et al.
Publicado: (2021)

MON-LB055 A Single Center Experience of Multiple Endocrine Neoplasia Type 1 (MEN1) vs Sporadic Insulinoma: What Can We Learn and Where Are We Going?
por: Itatani, Miho, et al.
Publicado: (2019)

SUN-933 Lactic Acidosis as a Rare and Unusual Presentation of Pheochromocytoma
por: Mohammad, Nazar, et al.
Publicado: (2020)

Presentation of Pheochromocytoma, Papillary Thyroid Cancer and Hyperparathyroidism in Three Family Members
por: Ashorobi, Damilola, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_h6nrjjdrpn8f8sh352e7s0j3qb