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Article

Multifocal renal oncocytoma in a patient with Von Hippel-Lindau mutation.

Urology - 1 Dec 2005

Fiske Joshua, Patel Rupa, Kau Eric, Pappas John G, Garcia Roberto A, Taneja Samir S

Abstract excerpt

Von Hippel-Lindau disease (VHL) is a rare genetic disease with a lifetime risk of clear cell renal cell carcinoma in approximately 70% of cases. We present a case of a 63-year-old man with bilateral, multifocal renal masses. Genetic testing results were consistent with a VHL deletion. The patient...

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Source

Identifiers

PMID: 16360474
DOI: 10.1016/j.urology.2005.06.122

Genes

VHL

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-16360474-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

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

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Multifocal renal oncocytoma in a patient with Von Hippel-Lindau mutation.PMID 16360474Read ↗

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[Von Hippel-Lindau syndrome - two sides of the same coin].Semantic proximity Read ↗

Comparison of clinical characteristics between patients with single mutation and co-mutation in hereditary renal cancer: a retrospective analysis of 115 patients with von Hippel-Lindau syndrome.Semantic proximity Read ↗

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