ALK-rearranged renal cell carcinoma with gains of chromosomes 7 and 17q --- A case report

Muntha Chaudhari, Hafiz Anas Yahya, Jianming Pei, Gabriel J. DiNatale, Iryna Mahan, James Ryan Mark, Arthur S. Patchefsky, Matthew R. Zibelman, Shuanzeng Wei

Research output: Contribution to journalArticlepeer-review

Abstract

ALK-rearranged renal cell carcinoma (ALK-RCC) is a rare subtype of RCC. In this report we describe the first ALK-RCC with gains of chromosome 7 and 17q. A 39-year-old male presented with an 11.5 cm renal mass and underwent a left radical nephrectomy. The tumor cells demonstrate focal clear cytoplasm, papillary formation, and extensive sarcomatoid changes. Molecular tests showed ALK rearrangement and gains at chromosomes 7 and 17q, which are commonly seen in papillary renal cell carcinoma. Thus caution is advised when interpreting chromosomal alterations for renal cell carcinoma.

Original languageEnglish
Article number103219
Pages (from-to)103219
JournalUrology Case Reports
Volume63
DOIs
StatePublished - Nov 2025

Keywords

  • ALK rearranged
  • Case report
  • Gains of chromosomes 7 and 17q
  • Renal cell carcinoma

Fingerprint

Dive into the research topics of 'ALK-rearranged renal cell carcinoma with gains of chromosomes 7 and 17q --- A case report'. Together they form a unique fingerprint.

Cite this