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Article

cDNA microarray analysis assists in diagnosis of malignant intrarenal pheochromocytoma originally masquerading as a renal cell carcinoma.

Journal of medical genetics - 1 Aug 2005

Takahashi M, Yang X J, McWhinney S, Sano N, Eng C, Kagawa S, Teh B T, Kanayama H-O

Abstract excerpt

Intrarenal pheochromocytoma (paraganglioma) is a very rare tumour. Its diagnosis is often difficult to establish because of its rarity and its histological similarity to renal cell carcinoma (RCC). Recently, we examined the molecular signatures of different subtypes of kidney tumours by using cDNA microarray. The signature pattern for one tumour, which was originally diagnosed as granular cell RCC, was clearly...

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Share to Carcinoma, Renal Cell
Share to Diagnosis, Differential

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to DNA, Complementary

Share to Kidney Neoplasms

Share to Oligonucleotide Array Sequence Analysis

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Share to Tomography, X-Ray Computed

Source

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Identifiers

PMID: 16061554
DOI: 10.1136/jmg.2005.031708
PMCID: PMC1736113

Genes

SDHD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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