| Literature DB >> 11381376 |
E Manegold1, L Tietze, K Günther, A Fleischer, B K Amo-Takyi, W Schröder, S Handt.
Abstract
Sertoli-Leydig cell tumors (SLCTs) represent a rare group of sex-cord stromal tumors of the ovary of unknown pathogenesis. We report a SLCT of intermediate differentiation with peritoneal recurrence and lymph node metastasis 12 months after removal, including cytogenetic analysis by comparative genomic hybridization and fluorescence in situ hybridization, which showed trisomy 8 as sole unbalanced karyotypic aberration. Our results provide evidence that a simple numeric chromosomal abnormality in SLCT may be associated with a malignant phenotype and suggest that the molecular pathogenesis of SLCT may be different from ovarian granulosa-stromal cell tumors.Entities:
Mesh:
Year: 2001 PMID: 11381376 DOI: 10.1053/hupa.2001.24316
Source DB: PubMed Journal: Hum Pathol ISSN: 0046-8177 Impact factor: 3.466