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A pediatric case of pheochromocytoma without apparent hypertension associated with von Hippel-Lindau disease.

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Clin Pediatr Endocrinol2018PMID 29662268PMC5897584stubpubmedProvenance
Source
PubMed
Retrieved
Sep 8, 2026
Layer
normalized (units and labels harmonized; values unchanged)
Run
ING-CIVIC-20260908-000001
Published

Abstract

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Linked entities

Linked entities (2)

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Validated 2

Curated evidence

Evidence citing this paper (1)

civicProvenance
Source
CIViC — Clinical Interpretation of Variants in Cancer
Dataset
CIViC evidence items
Version
civic-2026-09-08
Retrieved
Sep 8, 2026
Layer
normalized (units and labels harmonized; values unchanged)
Evidence
expert curation
License
CC0 1.0
PMID
29662268
Run
ING-CIVIC-20260908-000001
Open at source
CuratedShowing 1–1 of 1 evidence items · levels, directions and significance as curated at the source; each row links to its CIViC record.
TherapyCancerTypeLevelDirection · significanceRating (1–5)StatusEvidenceSource
VHL R161Q (c.482G>A)1
(predisposing)Von Hippel-Lindau DiseaseUNRESOLVEDPredisposingCSupports Predisposition3accepted
EID7141

A 12 year old Japanese female confirmed with the germline VHL mutation (c.482G>A) presented with pheochromocytoma. It was found that neither of her parents harboured this variation, confirming that sh… (full text at CIViC)

PMID 29662268 · Igaki et al., 2018 · Open in CIViC

civic