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About 7,822 results

ALLMedicine™ Pheochromocytoma Center

Research & Reviews  3,811 results

Characteristics of germline mutations in Korean patients with pheochromocytoma/paragang...
https://doi.org/10.1136/jmedgenet-2020-107102
Journal of Medical Genetics; Kim JH, Kim MJ et. al.

Nov 21st, 2020 - Pheochromocytomas and paragangliomas (PPGLs) are catecholamine-producing neuroendocrine tumours. PPGLs are a rare but important cause of secondary hypertension owing to their high morbidity and mortality. Patients with PPGL exhibit an increased pr...

Re-evaluating 'Surgical Dogma' in the Postoperative Management of Pheochromocytoma/Para...
https://doi.org/10.1007/s00268-020-05871-x
World Journal of Surgery; Pasieka JL

Nov 20th, 2020 - Re-evaluating 'Surgical Dogma' in the Postoperative Management of Pheochromocytoma/Paragangliomas: Reflecting on the Data Cannot Help but to Bring About Change.|2020|Pasieka JL,|

PET/CT in a patient with cardiac paraganglioma.
https://doi.org/10.1007/s10554-020-02101-2
The International Journal of Cardiovascular Imaging; Duan Y, Xu R et. al.

Nov 20th, 2020 - A 22-year-old female with SDHB-positive who presented with palpitation and hypertension after adrenalectomy was performed 18F-FDG PET/CT to detect the primary ectopic pheochromocytoma (PCC) and rule out metastasis. PET/CT is useful for detecting a...

The utility of 68Ga-DOTATATE PET/CT in localizing primary/metastatic pheochromocytoma a...
https://doi.org/10.1515/jpem-2020-0354
Journal of Pediatric Endocrinology & Metabolism : JPEM; Jaiswal SK, Sarathi V et. al.

Nov 12th, 2020 - Objectives Pediatric pheochromocytoma and paraganglioma (PPGL) are rare tumors with limited data on the diagnostic performance of 68Ga-DOTA(0)-Tyr(3)-octreotate positron emission tomography-computed tomography (68Ga-DOTATATE PET/CT). We have descr...

Algorithmic assessment of missense mutation severity in the Von-Hippel Lindau protein.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7644048
PloS One; Fields FR, Suresh N et. al.

Nov 5th, 2020 - Von Hippel-Lindau disease (VHL) is an autosomal dominant rare disease that causes the formation of angiogenic tumors. When functional, pVHL acts as an E3 ubiquitin ligase that negatively regulates hypoxia inducible factor (HIF). Genetic mutations ...

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Guidelines  9 results

Pheochromocytoma and Paraganglioma Treatment (PDQ®)–Health Professional Version
https://www.cancer.gov/types/pheochromocytoma/hp/pheochromocytoma-treatment-pdq

Sep 24th, 2019 - Pheochromocytoma and paraganglioma treatment is usually surgery, however, preoperative medical preparation is critical. Palliative care for metastatic disease may include chemotherapy, radiation therapy, targeted therapy, and other modalities. Get...

NCCN Guidelines Insights: Neuroendocrine and Adrenal Tumors, Version 2.2018
http://www.jnccn.org/content/16/6/693.full
Shah, M.

May 31st, 2018 - The NCCN Guidelines for Neuroendocrine and Adrenal Tumors provide recommendations for the management of adult patients with neuroendocrine tumors (NETs), adrenal gland tumors, pheochromocytomas, and paragangliomas. Management of NETs relies heavil.

Recommendations for the management of adrenal incidentalomas: what is pertinent for rad...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5605062
The British Journal of Radiology; Sahdev A

Feb 9th, 2017 - Adrenal incidentalomas are unsuspected, asymptomatic adrenal masses detected on imaging. Most are non-functioning benign adrenocortical adenomas but can represent other benign lesions or lesions requiring therapeutic intervention including adrenoc...

Management of adrenal incidentalomas: European Society of Endocrinology Clinical Practi...
https://doi.org/10.1530/EJE-16-0467
European Journal of Endocrinology; Fassnacht M, Arlt W et. al.

Jul 8th, 2016 - : By definition, an adrenal incidentaloma is an asymptomatic adrenal mass detected on imaging not performed for suspected adrenal disease. In most cases, adrenal incidentalomas are nonfunctioning adrenocortical adenomas, but may also represent con...

Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline.
https://doi.org/10.1210/jc.2014-1498
The Journal of Clinical Endocrinology and Metabolism; Lenders JW, Duh QY et. al.

Jun 3rd, 2014 - The aim was to formulate clinical practice guidelines for pheochromocytoma and paraganglioma (PPGL). The Task Force included a chair selected by the Endocrine Society Clinical Guidelines Subcommittee (CGS), seven experts in the field, and a method...

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Drugs  23 results see all →

Clinicaltrials.gov  3,901 results

Characteristics of germline mutations in Korean patients with pheochromocytoma/paragang...
https://doi.org/10.1136/jmedgenet-2020-107102
Journal of Medical Genetics; Kim JH, Kim MJ et. al.

Nov 21st, 2020 - Pheochromocytomas and paragangliomas (PPGLs) are catecholamine-producing neuroendocrine tumours. PPGLs are a rare but important cause of secondary hypertension owing to their high morbidity and mortality. Patients with PPGL exhibit an increased pr...

Re-evaluating 'Surgical Dogma' in the Postoperative Management of Pheochromocytoma/Para...
https://doi.org/10.1007/s00268-020-05871-x
World Journal of Surgery; Pasieka JL

Nov 20th, 2020 - Re-evaluating 'Surgical Dogma' in the Postoperative Management of Pheochromocytoma/Paragangliomas: Reflecting on the Data Cannot Help but to Bring About Change.|2020|Pasieka JL,|

PET/CT in a patient with cardiac paraganglioma.
https://doi.org/10.1007/s10554-020-02101-2
The International Journal of Cardiovascular Imaging; Duan Y, Xu R et. al.

Nov 20th, 2020 - A 22-year-old female with SDHB-positive who presented with palpitation and hypertension after adrenalectomy was performed 18F-FDG PET/CT to detect the primary ectopic pheochromocytoma (PCC) and rule out metastasis. PET/CT is useful for detecting a...

The utility of 68Ga-DOTATATE PET/CT in localizing primary/metastatic pheochromocytoma a...
https://doi.org/10.1515/jpem-2020-0354
Journal of Pediatric Endocrinology & Metabolism : JPEM; Jaiswal SK, Sarathi V et. al.

Nov 12th, 2020 - Objectives Pediatric pheochromocytoma and paraganglioma (PPGL) are rare tumors with limited data on the diagnostic performance of 68Ga-DOTA(0)-Tyr(3)-octreotate positron emission tomography-computed tomography (68Ga-DOTATATE PET/CT). We have descr...

Algorithmic assessment of missense mutation severity in the Von-Hippel Lindau protein.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7644048
PloS One; Fields FR, Suresh N et. al.

Nov 5th, 2020 - Von Hippel-Lindau disease (VHL) is an autosomal dominant rare disease that causes the formation of angiogenic tumors. When functional, pVHL acts as an E3 ubiquitin ligase that negatively regulates hypoxia inducible factor (HIF). Genetic mutations ...

see more →

News  63 results

Fast Five Quiz: Adrenal Gland Disorders
https://reference.medscape.com/viewarticle/922391

Dec 10th, 2019 - The adrenal glands are a pair of triangular glands, each about 2 inches long and 1 inch wide, that sit on top of the kidneys. They are responsible for the release of hormones that regulate metabolism, immune system function, and the salt-water bal...

Fast Five Quiz: Adrenal Gland Disorders
https://reference.staging.medscape.com/viewarticle/922391

Dec 10th, 2019 - The adrenal glands are a pair of triangular glands, each about 2 inches long and 1 inch wide, that sit on top of the kidneys. They are responsible for the release of hormones that regulate metabolism, immune system function, and the salt-water bal...

Pheochromocytoma and Paraganglioma Treatment (PDQ®)–Health Professional Version
https://www.cancer.gov/types/pheochromocytoma/hp/pheochromocytoma-treatment-pdq

Sep 24th, 2019 - Pheochromocytoma and paraganglioma treatment is usually surgery, however, preoperative medical preparation is critical. Palliative care for metastatic disease may include chemotherapy, radiation therapy, targeted therapy, and other modalities. Get...

A 34-Year-Old Man With a Severe Headache and Profuse Sweating: Osmosis USMLE Question
https://www.medscape.com/viewarticle/915630_2

Aug 8th, 2019 - Answer: E. Pheochromocytoma This man most likely has a pheochromocytoma, a rare tumor derived from the adrenal medulla that secretes the hormones of that organ: norepinephrine, epinephrine, and dopamine. Pheochromocytoma is characterized by paroxy...

What's New and Useful in Hypertension From ACC.19
https://www.medscape.com/viewarticle/911029

Mar 27th, 2019 - I have a special place in my heart for systemic arterial hypertension management. My brother had a pheochromocytoma that nearly killed him. I spent 5 days sweating on an IV magnesium drip filling one Foley bag after another when postpartum hyperte...

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Patient Education  15 results see all →