Detection of the ETV6-NTRK3 chimeric RNA of infantile fibrosarcoma/cellular congenital mesoblastic nephroma in paraffin-embedded tissue: Application to challenging pediatric renal stromal tumors

Pedram Argani, Michael Fritsch, Shri Hari S. Kadkol, Amy Schuster, J. Bruce Beckwith, Elizabeth J. Perlman

Research output: Contribution to journalArticle

Abstract

We report the development of a reverse transcriptase polymerase chain reaction assay that reliably detects the ETV6-NTRK3 chimeric RNA characteristic of infantile fibrosarcoma and the cellular variant of congenital mesoblastic nephroma (CMN) in formalin-fixed, paraffin-embedded tissue blocks. The 188 base pair polymerase chain reaction fusion product was detected in 11 of 12 cases of cellular CMN from which a larger sized control RNA band could be amplified, and even in 7 of 8 cases in which the control band was not detectable. A variety of other tumors that are in the histologic differential diagnosis of cellular CMN yielded negative results, including four classic CMNs, four rhabdoid tumors of the kidney, and four clear cell sarcomas of the kidney, confirming the assay's specificity. We further demonstrate the assay's utility by illustrating two cases of molecularly confirmed cellular CMN that mimicked rhabdoid tumor and clear cell sarcoma of the kidney. In contrast to previous reports, five mixed CMNs that had both classic and cellular areas all lacked the ETV6-NTRK3 fusion transcript. These results suggest that cases morphologically defined as mixed CMN may represent a mixed group of genetically distinct entities.

Original languageEnglish (US)
Pages (from-to)29-36
Number of pages8
JournalModern Pathology
Volume13
Issue number1
DOIs
StatePublished - Jan 2000

Keywords

  • Congenital mesoblastic nephroma
  • Infantile fibrosarcoma
  • Reverse transcriptase polymerase chain reaction

ASJC Scopus subject areas

  • Pathology and Forensic Medicine

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