Trisomies 8 and 20 characterize a subgroup of benign fibrous lesions arising in both soft tissue and bone.

Abstract

Trisomy 8 and trisomy 20 are nonrandom aberrations in desmoid tumors. The presence of these trisomies in related benign fibrous lesions of bone has not been previously addressed. In this study, 22 specimens from 19 patients diagnosed with desmoid tumor, desmoplastic fibroma, periosteal desmoid tumor, osteofibrous dysplasia, or fibrous dysplasia were examined by cytogenetic analysis of short-term cultures and bi-color fluorescence in situ hybridization of cytological touch preparations or paraffin-embedded tissue with centromeric probes for chromosomes 8 and 20. Trisomy 8 and trisomy 20 were detected by molecular cytogenetic methodologies in 15 specimens, including 10 primary bone lesions. Traditional cytogenetic analysis revealed trisomy 8 in two cases of osteofibrous dysplasia. Our findings demonstrate that trisomy 8 and trisomy 20 are also nonrandom aberrations in histologically similar, but clinically distinct, benign fibrous lesions of bone.

• Authors: J A Bridge, S J Swarts, C Buresh, M Nelson, J M Degenhardt, S Spanier, G Maale, A Meloni, J C Lynch, J R Neff
• Journal: The American journal of pathology (Am J Pathol) Vol. 154 Issue 3 Pg. 729-33 (Mar 1999) ISSN: 0002-9440 [Print] United States
• PMID: 10079250 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S.)

Topics

• Adolescent
• Adult
• Child
• Chromosomes, Human, Pair 20
• Chromosomes, Human, Pair 8
• Female
• Fibromatosis, Aggressive (genetics)
• Fibrous Dysplasia of Bone (genetics)
• Humans
• In Situ Hybridization, Fluorescence
• Karyotyping
• Male
• Middle Aged
• Trisomy