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About 7,546 results

ALLMedicine Pheochromocytoma Center

Research & Reviews  3,633 results

Stemness regulation of the adrenal mixed corticomedullary tumorigenesis-a case-control ...
https://doi.org/10.1016/j.neo.2020.04.003
Neoplasia (New York, N.Y.); Chiou HC, Jiang HJ et. al.

May 21st, 2020 - Mixed corticomedullary tumor is an adrenal tumor intermixed with cortical and medullary cells. It is extremely rare with unclear tumorigenesis. We reported a 32-year-old female, manifested with typical Cushing's syndrome and hypertension, to be di...

Prevalence and Incidence of Atrial Fibrillation in a Large Cohort of Adrenal Incidental...
https://doi.org/10.1210/clinem/dgaa270
The Journal of Clinical Endocrinology and Metabolism; Di Dalmazi G, Vicennati V et. al.

May 15th, 2020 - Chronic glucocorticoids excess leads to morphological and functional cardiac alterations, a substrate for arrhythmias. Autonomous cortisol secretion (ACS) in adrenal incidentalomas is a model of chronic endogenous hypercortisolism. To investigate ...

Bilateral pheochromocytoma: Clinical characteristics, treatment, and longitudinal follo...
https://doi.org/10.1111/cen.14222
Clinical Endocrinology; Kittah NE, Gruber LM et. al.

May 13th, 2020 - Comprehensive data about patients with bilateral pheochromocytoma is limited. We aimed to describe the clinical presentation, genetic analysis, treatment, and outcomes of patients with bilateral pheochromocytoma. A retrospective study at a tertiar...

MEN2-related pheochromocytoma: current state of knowledge, specific characteristics in ...
https://doi.org/10.1007/s12020-020-02332-2
Endocrine Vincent A, David T et. al.

May 10th, 2020 - Multiple endocrine neoplasia type 2 (MEN2) is a rare hereditary syndrome due to mutations of the proto-oncogene REarranged during Transfection (RET), defined by the association of medullary thyroid carcinoma (MTC) in almost 100% cases, and pheochr...

Anesthesia Management for Pediatric Patient With Multiple Endocrine Neoplasia Type 2B: ...
https://doi.org/10.1213/XAA.0000000000001215
A&A Practice; Allahyar AE, Liang X et. al.

May 5th, 2020 - Administering anesthesia to patients with pheochromocytoma may cause an exacerbation of catecholamine secretion from the pheochromocytoma secondary to drug administration, stress, or manipulation of the tumor. We present a pediatric patient with u...

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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  15 results see all →

Clinicaltrials.gov  3,763 results

Stemness regulation of the adrenal mixed corticomedullary tumorigenesis-a case-control ...
https://doi.org/10.1016/j.neo.2020.04.003
Neoplasia (New York, N.Y.); Chiou HC, Jiang HJ et. al.

May 21st, 2020 - Mixed corticomedullary tumor is an adrenal tumor intermixed with cortical and medullary cells. It is extremely rare with unclear tumorigenesis. We reported a 32-year-old female, manifested with typical Cushing's syndrome and hypertension, to be di...

Prevalence and Incidence of Atrial Fibrillation in a Large Cohort of Adrenal Incidental...
https://doi.org/10.1210/clinem/dgaa270
The Journal of Clinical Endocrinology and Metabolism; Di Dalmazi G, Vicennati V et. al.

May 15th, 2020 - Chronic glucocorticoids excess leads to morphological and functional cardiac alterations, a substrate for arrhythmias. Autonomous cortisol secretion (ACS) in adrenal incidentalomas is a model of chronic endogenous hypercortisolism. To investigate ...

Bilateral pheochromocytoma: Clinical characteristics, treatment, and longitudinal follo...
https://doi.org/10.1111/cen.14222
Clinical Endocrinology; Kittah NE, Gruber LM et. al.

May 13th, 2020 - Comprehensive data about patients with bilateral pheochromocytoma is limited. We aimed to describe the clinical presentation, genetic analysis, treatment, and outcomes of patients with bilateral pheochromocytoma. A retrospective study at a tertiar...

MEN2-related pheochromocytoma: current state of knowledge, specific characteristics in ...
https://doi.org/10.1007/s12020-020-02332-2
Endocrine Vincent A, David T et. al.

May 10th, 2020 - Multiple endocrine neoplasia type 2 (MEN2) is a rare hereditary syndrome due to mutations of the proto-oncogene REarranged during Transfection (RET), defined by the association of medullary thyroid carcinoma (MTC) in almost 100% cases, and pheochr...

Anesthesia Management for Pediatric Patient With Multiple Endocrine Neoplasia Type 2B: ...
https://doi.org/10.1213/XAA.0000000000001215
A&A Practice; Allahyar AE, Liang X et. al.

May 5th, 2020 - Administering anesthesia to patients with pheochromocytoma may cause an exacerbation of catecholamine secretion from the pheochromocytoma secondary to drug administration, stress, or manipulation of the tumor. We present a pediatric patient with u...

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News  111 results

Fast Five Quiz: Adrenal Gland Disorders
https://www.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...

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...

FDA approves radioactive agent for adrenal tumors
https://www.mdedge.com/hematology-oncology/article/171523/genitourinary-cancer/fda-approves-radioactive-agent-adrenal?channel=39313
Christopher Palmer

Jul 31st, 2018 - The Food and Drug Administration has approved iobenguane I 131 injection (Azedra) for intravenous use for the treatment of adults and adolescents aged 12 years and older with rare adrenal tumors (pheochromocytoma or paraganglioma) that are unresec.

FDA approves Progenics' treatment for rare adrenal gland tumors
https://www.reuters.com/article/us-progenics-pharm-fda/fda-approves-progenics-treatment-for-rare-adrenal-gland-tumors-idUSKBN1KK2C2

Jul 30th, 2018 - (Reuters) - The U.S. Food and Drug Administration (FDA) on Monday approved Progenics Pharmaceuticals Inc’s treatment for two types of rare adrenal gland tumors, making it the first drug approved in the United States for this use. The drug, Azedra,...

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Patient Education  15 results see all →