Abstract
Four case reports of mesenchymal neoplasms showing chromosomal abnormalities are presented. In a case of hemangiopericytoma trisomy 2 and centric fusion 19;21 were present. In a mastocytoma a deleted chromosome 35 was seen. A homogeneously staining region (HSR) on chromosome 1 was detected in a histiocytoma. Trisomy 5 and monosomy 31 were observed in a case of granulocytic sarcoma (chloroma). The lack of mutations in exons 1 and 2 of oncogenes N-ras, K-ras, and H-ras and exons 5, 6, 7, and 8 of tumor suppressor gene p53 in these four patients and in a larger series of investigated dogs (25 hemangiopericytomas, 12 mastocytomas, and 8 histiocytomas) is highlighted.
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CITATION STYLE
Mayr, B., Reifinger, M., Brem, G., Feil, C., & Schleger, W. (1999). Cytogenetic, ras, and p53: Studies in cases, of canine neoplasms (hemangiopericytoma, mastocytoma, histiocytoma, chloroma). In Journal of Heredity (Vol. 90, pp. 124–128). https://doi.org/10.1093/jhered/90.1.124
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