Reverse transcriptase-polymerase chain reaction as an ancillary molecular technique in the diagnosis of small blue round cell tumors by fine-needle aspiration cytology

Am J Clin Pathol. 2010 Apr;133(4):633-45. doi: 10.1309/AJCPPJJ0PY4XZOEC.

Abstract

We evaluated the feasibility and usefulness of reverse transcriptase-polymerase chain reaction (RT-PCR) on fine-needle aspirates for categorization of small blue round cell tumors (SBRCTs). A total of 51 cases, including 25 Ewing sarcoma/peripheral primitive neuroectodermal tumors (PNETs), 11 rhabdomyosarcomas, 13 neuroblastomas, and 2 desmoplastic small round cell tumors (DSRCTs) were analyzed. The detection of the EWS-FLI1 (20/25) and EWS-ERG (4/25) fusion transcripts resolved 24 of 25 cases of Ewing sarcoma/PNET. The PAX3/7-FKHR fusion transcript was detected in 2 of 4 cases of alveolar rhabdomyosarcoma and the EWS-WT1 transcript in both cases of DSRCT. Tyrosine hydroxylase and 3,4-dihydroxyphenylalanine (dopa) decarboxylase transcripts were demonstrated in 10 of 13 cases of neuroblastoma. In comparison, immunocytochemical analysis resolved 19 (76%) of 25 Ewing sarcomas, 9 (82%) of 11 rhabdomyosarcomas, 6 (46%) of 13 neuroblastomas, and 1 (50%) of 2 DSRCTs. Overall, RT-PCR resolved 38 (86%) of 44 vs 35 (69%) of 51 cases by immunocytochemical analysis. RT-PCR is easily applied to fine-needle aspirates of SBRCT and greatly facilitates accurate tumor typing.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Biopsy, Fine-Needle / methods*
  • Humans
  • Neuroblastoma / diagnosis*
  • Neuroblastoma / drug therapy
  • Neuroblastoma / genetics
  • Neuroectodermal Tumors, Primitive, Peripheral / diagnosis*
  • Neuroectodermal Tumors, Primitive, Peripheral / drug therapy
  • Neuroectodermal Tumors, Primitive, Peripheral / genetics
  • Reverse Transcriptase Polymerase Chain Reaction / methods*
  • Rhabdomyosarcoma / diagnosis*
  • Rhabdomyosarcoma / drug therapy
  • Rhabdomyosarcoma / genetics
  • Sarcoma, Ewing / diagnosis*
  • Sarcoma, Ewing / drug therapy
  • Sarcoma, Ewing / genetics
  • Sarcoma, Small Cell / diagnosis*
  • Sarcoma, Small Cell / drug therapy
  • Sarcoma, Small Cell / genetics
  • Soft Tissue Neoplasms / diagnosis*
  • Soft Tissue Neoplasms / drug therapy
  • Soft Tissue Neoplasms / genetics