Abstract
We report a patient with a recurrent chondromyxoid fibroma, a rare benign tumor of the bone with clonal aberrations in chromosomes 2 and 5. Karyotyping, chromosome painting, interphase cytogenetics by in situ hybridization, and DNA flow cytometry were used. The karyotype was interpreted as 46,XX,der(2)ins(5;2)(q13;p21p25),der(2)ins(5;2)(q13;p21p25), der(5)ins(5;2) (q13;p21p25).
Publication types
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Case Reports
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Research Support, Non-U.S. Gov't
MeSH terms
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Adult
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Bone Neoplasms / genetics*
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Bone Neoplasms / surgery
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Chondroma / genetics*
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Chondroma / surgery
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Chromosomes, Human, Pair 1
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Chromosomes, Human, Pair 12
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Chromosomes, Human, Pair 2*
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Chromosomes, Human, Pair 5*
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Chromosomes, Human, Pair 7
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DNA, Neoplasm / analysis
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Female
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Humans
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Karyotyping
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Neoplasm Recurrence, Local / genetics*
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Neoplasm Recurrence, Local / surgery
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Radius* / surgery
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Reoperation
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Translocation, Genetic / genetics*
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Trisomy