Unstable translocation (8;22) in a case of giant cell reparative granuloma

Cancer Genetics and Cytogenetics

Volumn 177, Issue 1, 2007, Pages 59-63

  Johnsson, Anna ^a   Collin, Anna ^a   Rydholm, Anders ^a   Domanski, Henryk A ^a   Mertens, Fredrik ^a   Mandahl, Nils ^a  

^a LUND UNIVERSITY HOSPITAL   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHROMOSOME 22Q; CHROMOSOME 8P; CHROMOSOME 8Q; CHROMOSOME ABERRATION; CHROMOSOME BANDING PATTERN; CURETTAGE; CYTOGENETICS; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GIANT CELL REPARATIVE GRANULOMA; GIANT CELL TUMOR; HUMAN; HUMAN TISSUE; METACARPAL BONE; PRIORITY JOURNAL; SKIN BIOPSY; THUMB; TREATMENT OUTCOME; TUMOR DIAGNOSIS;

BONE DISEASES; CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 22; CHROMOSOMES, HUMAN, PAIR 8; FEMALE; GRANULOMA, GIANT CELL; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MIDDLE AGED; TRANSLOCATION, GENETIC;

EID: 34547682282     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cancergencyto.2007.04.017     Document Type: Article

References (18)

1. Murphey M.D., Nomikos G.C., Flemming D.J., Gannon F.H., Temple T., and Kransdorf M.J. From the archives of the AFIP. Imaging of giant cell tumor and giant cell reparative granuloma of bone: radiologic-pathologic correlation. RadioGraphics 21 (2001) 1283-1309
2. Macdonald D.F., Binhammer P.A., Rubenstein J.D., and Fornasier V.L. Giant cell reparative granuloma of the hand: case report and review of giant cell lesions of hands and feet. Can J Surg 46 (2003) 471-473
3. Biscaglia R., Bacchini P., and Bertoni F. Giant cell tumor of the bones of the hand and foot. Cancer 88 (2000) 2022-2032
4. Buresh C.J., Seemayer T.A., Nelson M., Neff J.R., Dorfman H.D., and Bridge J. t(X;4)(q22;q31.3) in giant cell reparative granuloma. Cancer Genet Cytogenet 115 (1999) 80-81
5. Schwartz H.S., Butler M.G., Jenkins R.B., Miller D.A., and Moses H.L. Telomeric associations and consistent growth factor overexpression detected in giant cell tumor of bone. Cancer Genet Cytogenet 56 (1991) 263-276
6. Bridge J.A., Neff J.R., and Mouron B.J. Giant cell tumor of bone. Chromosomal analysis of 48 specimens and review of the literature. Cancer Genet Cytogenet 58 (1992) 2-13
7. Sciot R., Dorfman H., Brys P., Dal Cin P., De Wever I., Fletcher C.D.M., Jonsson K., Mandahl N., Mertens F., Mitelman F., Rosai J., Rydholm A., Samson I., Tallini G., Van den Berghe H., Vanni R., and Willén H. Cytogenetic-morphologic correlations in aneurysmal bone cyst, giant cell tumor of bone and combined lesions. A report from the CHAMP study group. Mod Pathol 13 (2000) 1206-1210
8. Althof P.A., Ohmori K., Zhou M., Bailey J.M., Bridge R.S., Nelson M., Neff J.R., and Bridge J.A. Cytogenetic and molecular cytogenetic findings in 43 aneurysmal bone cysts: aberrations of 17p mapped to 17p13.2 by fluorescence in situ hybridization. Mod Pathol 17 (2004) 518-525
9. Oliveira A.M., Hsi B.-L., Weremowicz S., Rosenberg A.E., Dal Cin P., Joseph N., Bridge J.A., Perez-Atayde A.R., and Fletcher J.A. USP6 (Tre2) fusion oncogenes in aneurysmal bone cyst. Cancer Res 64 (2004) 1920-1923
10. Oliveira A.M., Perez-Atayde A.R., Dal Cin P., Gebhardt M.C., Chen C.-J., Neff J.R., Demetri G.D., Rosenberg A.E., Bridge J.A., and Fletcher J.A. Aneurysmal bone cyst variant translocations upregulate USP6 transcription by promoter swapping with the ZNF9, COL1A1, TRAP150, and OMD genes. Oncogene 24 (2005) 3419-3426
11. Mandahl N., Heim S., Arheden K., Rydholm A., Willén H., and Mitelman F. Three major cytogenetic subgroups can be identified among chromosomally abnormal solitary lipomas. Hum Genet 79 (1988) 203-208
12. Dahlén A., Debiec-Rychter M., Pedeutour F., Domanski H.A., Höglund M., Bauer H.C.F., Rydholm A., Sciot R., Mandahl N., and Mertens F. Clustering of deletions on chromosome 13 in benign and low-malignant lipomatous tumors. Int J Cancer 103 (2003) 616-623
13. Tanke H., Wiegant J., van Gijlswijk R.P.M., Bezrookove V., Pattenier H., Heetebrij R.J., Talman E.G., Raap A.K., and Vrolijk J. New strategy for multi-colour fluorescence in situ hybridisation: COBRA: COmbined Binary RAtio labelling. Eur J Hum Genet 7 (1999) 2-11
14. Nilsson M., Domanski H., Mertens F., and Mandahl N. Atypical lipomatous tumor with rare structural rearrangements involving chromosomes 8 and 12. Oncol Reports 13 (2005) 649-652
15. Gisselsson D., Pettersson L., Höglund M., Heidenblad M., Gorunova L., Wiegant J., Mertens F., Dal Cin P., Mitelman F., and Mandahl N. Chromosomal breakage-fusion-bridge events cause genetic intratumor heterogeneity. Proc Natl Acad Sci USA 97 (2000) 5357-5362
16. Gisselsson D., Jonson T., Petersén A., Strömbeck B., Dal Cin P., Höglund M., Mitelman F., Mertens F., and Mandahl N. Telomere dysfunction triggers extensive DNA fragmentation and evolution of complex chromosome abnormalities in human malignant tumors. Proc Natl Acad Sci USA 98 (2001) 12683-12688
17. Sawyer J.R., Goosen L.S., Binz R.L., Swanson C.M., and Nicholas R.W. Evidence for telomeric fusions as a mechanism for recurring structural aberrations of chromosome 11 in giant cell tumors of bone. Cancer Genet Cytogenet 159 (2005) 32-36
18. Mandahl N., Mertens F., Willén H., Rydholm A., Kreicbergs A., and Mitelman F. Nonrandom pattern of telomeric associations in lipomatous tumors with ring and giant marker chromosomes. Cancer Genet Cytogenet 103 (1998) 25-34