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

Pheochromocytoma in an 8-year-old patient with multiple endocrine neoplasia type 2A: implications for screening.

Journal of surgical oncology - 1 Sept 2013

Rowland Kathryn J, Chernock Rebecca D, Moley Jeffrey F

Abstract excerpt

Childhood pheochromocytoma in the setting of multiple endocrine neoplasia type 2 (MEN2) remains rare and has not been reported under the age of 12. We present an 8-year-old female with known MEN 2A, C634Y RET mutation, diagnosed with a 6 cm pheochromocytoma requiring laparoscopic adrenalectomy. G...

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 Child
Share to Early Detection of Cancer

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to RET gene

Share to Multiple Endocrine Neoplasia Type 2a

Share to Mutation

Share to Pheochromocytoma

Share to Proto-Oncogene Proteins c-ret

Source

Open in PubMed Open full text

Identifiers

PMID: 23868299
DOI: 10.1002/jso.23378
PMCID: PMC3983847

Genes

RET

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-23868299-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Pheochromocytoma in an 8-year-old patient with multiple endocrine neoplasia type 2A: implications for screening.PMID 23868299Read ↗

Phaeochromocytoma in multiple endocrine neoplasia type 2: RET codon‐specific penetrance and changes in management during the last four decadesSemantic proximity Read ↗

[The clinical patterns and RET proto-oncogene identification of pheochromocytoma in 13 multiple endocrine neoplasia type 2A pedigrees].Semantic proximity Read ↗

Hereditary medullary thyroid carcinoma: how molecular genetics made multiple endocrine neoplasia type 2 a paediatric disease.Semantic proximity Read ↗

Multiple endocrine neoplasia type 2B--genetic basis and clinical expression.Semantic proximity Read ↗

The clinical spectrum of multiple endocrine neoplasia type 2a caused by the rare intracellular RET mutation S891A.Semantic proximity Read ↗

100-Year evolution of precision medicine and surgery for multiple endocrine neoplasia type 2A.Semantic proximity Read ↗

The RET E616Q Variant is a Gain of Function Mutation Present in a Family with Features of Multiple Endocrine Neoplasia 2A.Semantic proximity Read ↗

A newly detected mutation of the RET protooncogene in exon 8 as a cause of multiple endocrine neoplasia type 2A.Semantic proximity Read ↗

Late diagnosis of type 2B multiple endocrine neoplasia (MEN 2B) in a 23 year-old patient.Semantic proximity Read ↗

Pheochromocytomas in Multiple Endocrine Neoplasia Type 2.Semantic proximity Read ↗

Pheochromocytoma: a review.Semantic proximity Read ↗

RET proto-oncogene testing in infants presenting with Hirschsprung disease identifies 2 new multiple endocrine neoplasia 2A kindreds.Semantic proximity Read ↗

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