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Is 4q13 a recurring breakpoint in solitary fibrous tumors?
M Debiec-Rychter1, I de Wever, A Hagemeijer
1Center of Human Genetics, Katholieke Universiteit Leuven, 49, B-3000 Leuven, Herestraat, Belgium. maria.debiec-rychter@med.kuleuven.ac.be
Abstract:
Solitary fibrous tumor (SFT) is a mesenchymal neoplasm found predominantly in the subpleural region but also in many other body sites. We report a malignant solitary fibrous tumor of the peritoneum with a 47,XY,t(4;9)(q13;p23),+5 karyotype. The chromosome 4q13 breakpoint in the presented and previously published case of pleural solitary fibrous tumor with a 46,XY,t(4;15)(q13;q26) karyotype was further characterized by fluorescence in situ hybridization analysis and localized within the 5-cM interval that was flanked by regions specific to YAC clones 761A7 and 886C11. Chromosome translocations involving chromosome 4q13 may characterize a separate cytogenetic subgroup of SFT.