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About 7,674 results

ALLMedicine™ Pheochromocytoma Center

Research & Reviews  3,769 results

Patients with pheochromocytoma exhibit low aldosterone renin ratio-preliminary reports.
https://doi.org/10.1186/s12902-020-00620-6
BMC Endocrine Disorders; Yamada T, Fukuoka H et. al.

Sep 12th, 2020 - Plasma renin activity (PRA) is generally increased in patients with pheochromocytoma (PCC) due to low circulating plasma volume and activation of β-1 adrenergic receptor signaling. However, there has been no study on the aldosterone renin ratio (A...

Molecular diagnosis and treatment of multiple endocrine neoplasia type 2B in Ethnic Han...
https://doi.org/10.2174/1871530320666200910112230
Endocrine, Metabolic & Immune Disorders Drug Targets; Zhang ZW, Guo X et. al.

Sep 11th, 2020 - Multiple endocrine neoplasia type 2B (MEN 2B) is mainly caused by M918T RET germline mutation, and characterized by medullary thyroid carcinoma (MTC), pheochromocytoma (PHEO) and non-endocrine features. However, the diagnosis and treatment are usu...

Child Neurology: Pheochromocytoma unveiled by reversible cerebral vasoconstriction synd...
https://doi.org/10.1212/WNL.0000000000010801
Neurology Lagacé M, Graeber B et. al.

Sep 10th, 2020 - Child Neurology: Pheochromocytoma unveiled by reversible cerebral vasoconstriction syndrome in a child with NF-1.|2020|Lagacé M,Graeber B,Huh L,|

FDG PET/CT Findings in a Patient With Ovarian Metastasis of Pheochromocytoma.
https://doi.org/10.1097/RLU.0000000000003269
Clinical Nuclear Medicine; Jiang Y, Hou G et. al.

Sep 10th, 2020 - Pheochromocytoma metastasizing to the ovary is extremely rare. We report the case of a 59-year-old woman who underwent right adrenal pheochromocytoma resection 14 years ago and remained asymptomatic until recently when she complained of palpitatio...

Laparoscopic transperitoneal left partial adrenalectomy for familial pheochromocytoma (...
https://doi.org/10.1016/j.jviscsurg.2020.08.007
Journal of Visceral Surgery; Najah H, Gaye D et. al.

Sep 6th, 2020 - Laparoscopic transperitoneal left partial adrenalectomy for familial pheochromocytoma (with video).|2020|Najah H,Gaye D,Haissaguerre M,|

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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  19 results see all →

Clinicaltrials.gov  3,827 results

Neuroendocrine tumors - Care at Mayo Clinic - Mayo Clinic
https://www.mayoclinic.org/diseases-conditions/neuroendocrine-tumors/care-at-mayo-clinic/mac-20354135

Sep 15th, 2020 - Neuroendocrine tumors care at Mayo Clinic Mayo Clinic experts are skilled in the diagnosis and treatment of neuroendocrine tumors, including: Neuroendocrine tumors of the digestive system and pancreas, sometimes called gastroenteropancreatic neuro...

Patients with pheochromocytoma exhibit low aldosterone renin ratio-preliminary reports.
https://doi.org/10.1186/s12902-020-00620-6
BMC Endocrine Disorders; Yamada T, Fukuoka H et. al.

Sep 12th, 2020 - Plasma renin activity (PRA) is generally increased in patients with pheochromocytoma (PCC) due to low circulating plasma volume and activation of β-1 adrenergic receptor signaling. However, there has been no study on the aldosterone renin ratio (A...

Molecular diagnosis and treatment of multiple endocrine neoplasia type 2B in Ethnic Han...
https://doi.org/10.2174/1871530320666200910112230
Endocrine, Metabolic & Immune Disorders Drug Targets; Zhang ZW, Guo X et. al.

Sep 11th, 2020 - Multiple endocrine neoplasia type 2B (MEN 2B) is mainly caused by M918T RET germline mutation, and characterized by medullary thyroid carcinoma (MTC), pheochromocytoma (PHEO) and non-endocrine features. However, the diagnosis and treatment are usu...

Child Neurology: Pheochromocytoma unveiled by reversible cerebral vasoconstriction synd...
https://doi.org/10.1212/WNL.0000000000010801
Neurology Lagacé M, Graeber B et. al.

Sep 10th, 2020 - Child Neurology: Pheochromocytoma unveiled by reversible cerebral vasoconstriction syndrome in a child with NF-1.|2020|Lagacé M,Graeber B,Huh L,|

FDG PET/CT Findings in a Patient With Ovarian Metastasis of Pheochromocytoma.
https://doi.org/10.1097/RLU.0000000000003269
Clinical Nuclear Medicine; Jiang Y, Hou G et. al.

Sep 10th, 2020 - Pheochromocytoma metastasizing to the ovary is extremely rare. We report the case of a 59-year-old woman who underwent right adrenal pheochromocytoma resection 14 years ago and remained asymptomatic until recently when she complained of palpitatio...

see more →

News  35 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...

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,...

A rare case of hypoglycemia induced by a classic gastrointestinal stromal tumor
https://www.mdedge.com/hematology-oncology/article/141476/gastroenterology/rare-case-hypoglycemia-induced-classic
Gupta et al

Jun 29th, 2017 - Hypoglycemia, a frequently encountered medical emergency, is usually seen in patients with diabetes, most commonly as a result of iatrogenesis. However, it can also be encountered in nondiabetic patients.

Pheochromocytoma linked to higher risk of postop complications
https://www.mdedge.com/internalmedicine/article/131839/general-surgery/pheochromocytoma-linked-higher-risk-postop
Michele G. Sullivan

Feb 21st, 2017 - LAS VEGAS – Patients with pheochromocytoma are likely to have preoperative comorbidities that predispose them to postoperative cardiopulmonary complications, leading to a longer length of stay and greater hospital charges. A 5-year national databa.

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Patient Education  15 results see all →