Significance of abnormalities of chromosomes 5 and 8 in chondroblastoma

Clinical Orthopaedics and Related Research

Volumn 349, Issue , 1998, Pages 189-193

  Swarts, Sarah J ^a   Neff, James R ^a   Johansson, Sonny L ^a   Nelson, Mari ^a   Bridge, Julia A ^a,b  

^a UNIVERSITY OF NEBRASKA MEDICAL CENTER   (United States)

^b UNIVERSITY OF NEBRASKA AT OMAHA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; BONE TUMOR; CASE REPORT; CHONDROBLASTOMA; CHROMOSOME 5; CHROMOSOME 8; CHROMOSOME ABERRATION; CYTOGENETICS; HUMAN; HUMAN CELL; KARYOTYPE; MALE; PRIORITY JOURNAL;

EID: 0031967861     PISSN: 0009921X     EISSN: 15281132     Source Type: Journal    
DOI: 10.1097/00003086-199804000-00023     Document Type: Article

References (20)

1. Ahn J, Lüdecke HJ, Lindow S, et al: Cloning of the putative tumor suppressor gene for hereditary multiple exostoses (EXT1). Nature Genetics 11:137-143, 1995.
2. Bridge JA: Cytogenetic and molecular cytogenetic techniques in orthopaedic surgery. J Bone Joint Surg 75A:606-614, 1993.
3. Bridge JA: Cytogenetic and experimental models of sarcomas. Curr Opin Oncol 333-339, 1995.
4. Bridge JA, Bhatia PS, Andersen JR, Neff JR: Biologic and clinical significance of cytogenetic and molecular cytogenetic abnormalities in benign and malignant cartilaginous lesions. Cancer Genet Cytogenet 69:79-90, 1993.
5. Bridge JA, Sanger WG, Neff JR: Translocations involving chromosomes 2 and 13 in benign and malignant cartilaginous neoplasms. Cancer Genet Cytogenet 38:83-88, 1989.
6. Bridge JA, Sreekantaiah C, Mouron B, et al: Clonal chromosomal abnormalities in desmoid tumors: Implications for histopathogenesis. Cancer 69: 430-436, 1992.
7. Demetrick DJ, Zhang H, Beach DH: Chromosomal mapping of the human genes CKS1 to 8q21 and CKS2 to 9q22. Cytogenet Cell Genet 73:250-254, 1996.
8. Greco A, Ittman M, Barletta C, et al: Chromosomal localization of human genes required for G1 progression in mammalian cells. Genomics 4:240-245, 1989.
9. Huvos AG: Bone Tumors. Diagnosis, Treatment, and Prognosis. Philadelphia, WB Saunders Co 295-318, 1991.
10. Kahn LB, Wood FM, Ackerman LV: Malignant chondroblastoma. Report of two cases and review of the literature. Arch Pathol 88:371-376, 1969.
11. Kunkel MG, Dahlin DC, Young HH: Benign chondroblastoma. J Bone Joint Surg 38A:317-322, 1956.
12. Kunze E, Graewe TH, Peitsch E: Histology and biology of metastatic chondroblastoma. Review of a case with a review of the literature. Pathol Res Pract 182:113-120, 1987.
13. Mark J, Wedell B, Dahlenfors R, Grepp C, Burian P: Human benign chondroblastoma with a pseudodiploid stemline characterized by a complex and balanced translocation. Cancer Genet Cytogenet 58:14-17, 1992.
14. McBryde Jr A, Goldner JL: Chondroblastoma of bone. Am J Surg 36:94-108, 1970.
15. Mertens F, Rydholm A, Kreicbergs A, et al: Loss of chromosome band 8q24 in sporadic osteocartilaginous exostoses. Genes Chromosom Cancer 9:8-12, 1994.
16. Mitelman F (ed): An International System for Human Cytogenetic Nomenclature. Basel, Karger 1-85, 1995.
17. Reyes CV, Kathuria S: Recurrent and aggressive chondroblastoma of the pelvis with late neoplastic changes. Am J Surg Pathol 3:449-455, 1979.
18. Sandberg AA, Bridge JA: The Cytogenetics of Bone and Soft Tissue Tumors. Austin, RG Landes 7:322-323, 1994.
19. Tarkkanen M, Böhling T, Heliö H, et al: A recurrent chondromyxoid fibroma with chromosome aberrations ins(5;2)(q13;p21p25) and 2p deletion: A case report. Cancer Genet Cytogenet 65:141-146, 1993.
20. Tarkkanen M, Kaipainen A, Karaharju E, et al: Cytogenetic study of 269 consecutive patients examined for a bone tumor. Cancer Genet Cytogenet 68:1-21, 1993.