Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Molecular and therapeutic advances in the diagnosis and management of malignant pheochromocytomas and paragangliomas.

The oncologist - 1 Jan 2013

Lowery Aoife J, Walsh Siun, McDermott Enda W, Prichard Ruth S

Abstract excerpt

Pheochromocytomas (PCCs) and paragangliomas (PGLs) are rare catecholamine-secreting tumors derived from chromaffin cells originating in the neural crest. These tumors represent a significant diagnostic and therapeutic challenge because the diagnosis of malignancy is frequently made in retrospect by the development of metastatic or recurrent disease. Complete surgical resection offers the only potential for cure;...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adrenal Gland Neoplasms
Share to Adrenalectomy
Share to Diagnostic Imaging

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to MicroRNAs

Share to Neoplasm Recurrence, Local

Share to Paraganglioma

Share to Pheochromocytoma

Share to Prognosis

Source

Open in PubMed Open full text

Identifiers

PMID: 23576482
DOI: 10.1634/theoncologist.2012-0410
PMCID: PMC3639526

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Molecular and therapeutic advances in the diagnosis and management of malignant pheochromocytomas and paragangliomas.PMID 23576482Read ↗

Update of Pheochromocytoma Syndromes: Genetics, Biochemical Evaluation, and ImagingSemantic proximity Read ↗

Multidisciplinary practice guidelines for the diagnosis, genetic counseling and treatment of pheochromocytomas and paragangliomas.Semantic proximity Read ↗

Pheochromocytoma and Paraganglioma: Genetics, Diagnosis, and Treatment.Semantic proximity Read ↗

Pheochromocytomas and Paragangliomas: From Genetic Diversity to Targeted TherapiesSemantic proximity Read ↗

Current Management of Pheochromocytoma/Paraganglioma: A Guide for the Practicing Clinician in the Era of Precision MedicineSemantic proximity Read ↗

Pheochromocytomas and Paragangliomas: New Developments with Regard to Classification, Genetics, and Cell of OriginSemantic proximity Read ↗

Diagnosis for Pheochromocytoma and Paraganglioma: A Joint Position Statement of the Korean Pheochromocytoma and Paraganglioma Task ForceSemantic proximity Read ↗

Clinical Syndromes and Genetic Screening Strategies of Pheochromocytoma and ParagangliomaSemantic proximity Read ↗

Pheochromocytomas and Paragangliomas: An Update on Recent Molecular Genetic Advances and Criteria for Malignancy.Semantic proximity Read ↗

Pheochromocytoma: current approaches and future directions.Semantic proximity Read ↗

Rethinking pheochromocytomas and paragangliomas from a genomic perspective.Semantic proximity Read ↗

Pheochromocytoma/paraganglioma: recent updates in genetics, biochemistry, immunohistochemistry, metabolomics, imaging and therapeutic optionsSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.