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2 Jul 2014 CHICAGO – Genetic testing has jumped to the fore in the management of patients diagnosed as having a pheochromocytoma or paraganglioma, according to new clinical practice guidelines released by the Endocrine Society. Indeed, the new guidelines call for genetic testing to be considered seriously in
Objective: The aim was to formulate clinical practice guidelines for pheochromocytoma and paraganglioma (PPGL). Participants: The Task Force included a chair selected by the Endocrine Society Clinical Guidelines Subcommittee (CGS), seven experts in the field, and a methodologist. The authors received no corporate
11 Apr 2016 Patients who have undergone surgery to remove a pheochromocytoma or paraganglioma should be followed for at least 10 years to assess for local or metastatic tumor recurrence, according to a new clinical practice guideline released by the European Society of Endocrinology. The incidence of tumor
10 Oct 2017 In 2014, the Endocrine Society (ES), the American Association for Clinical Chemistry (AACC), and the European Society of Endocrinology (ESE) released joint clinical practice guidelines for the management of pheochromocytoma and paraganglioma (referred to together as PPGL). The guidelines include
The North American Neuroendocrine Tumor Society consensus guideline for the diagnosis and management of neuroendocrine tumors: pheochromocytoma, paraganglioma, and medullary thyroid cancer. Published by: North American Neuroendocrine Tumor Society. Last published: 2010
The Clinical Guidelines Subcommittee (CGS) of the Endocrine Society deemed the diagnosis of pheochromocytoma and paraganglioma a priority area in need of practice guidelines and appointed a Task Force to formulate evidence-based
1 May 2016 The present guideline aims to propose standardised clinical care of long-term follow-up in patients operated on for a PPGL. The guideline has been developed by The European Society of Endocrinology and based on the Grading of Recommendations Assessment, Development and Evaluation (GRADE)

We continually create new guidelines and update existing guidelines to reflect the changing clinical science and meet the needs of practicing physicians. See our upcoming topics and updates to learn which guideline topics are in progress. Diagnosis and Treatment of Pheochromocytoma and Paraganglioma | 2014
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March 2018