der(16)t(1;16)(q21;q13) as a secondary change in alveolar rhabdomyosarcoma: A case report and review of the literature

Cancer Genetics and Cytogenetics

Volumn 87, Issue 2, 1996, Pages 179-181

  McManus, Aidan P ^a   Min, Toon ^a   Swansbury, G John ^a   Gusterson, Barry A ^a   Pinkerton, C Ross ^a   Shipley, Janet M ^a  

^a INSTITUTE OF CANCER RESEARCH   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CARCINOGENESIS; CASE REPORT; CHILDHOOD CANCER; CHROMOSOME 1Q; CHROMOSOME TRANSLOCATION 1; CHROMOSOME TRANSLOCATION 16; CYTOGENETICS; HUMAN; MALE; MUSCLE CELL; PRIORITY JOURNAL; RHABDOMYOSARCOMA; SCHOOL CHILD; TRISOMY;

EID: 0029932287     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/0165-4608(95)00267-7     Document Type: Article

References (14)

1. Variend S (1985): Small cell tumours in childhood: a review. J Pathol 145:1-25.
2. Tsokos M, Webber BL, Parham DM, Wesley RA, Miser A, Miser JS, Etcubanas E, Kinsella T, Grayson J, Glatstein E (1992): Rhabdomyosarcoma - a new classification scheme related to prognosis. Arch Pathol Lab Med 116:847-855.
3. Mitelman F (1994): Catalog of Chromosome Aberrations in cancer. New York, Wiley-Liss.
4. Sandberg AA, Bridge JA (1994): The Cytogenetics of Bone and Soft Tissue Tumors. Austin, R.G. Landes Company.
5. Scrable H, Witte D, Shimada H, Seemayer T, Wang-Wuu S, Soukup S, Koufos A, Houghton P, Lampkin B, Cavenee W (1989): Molecular differential pathology of rhabdomyosarcoma. Genes Chrom Cancer 1:23-35.
6. Atkin NB (1986): Chromosome 1 aberrations in cancer. Cancer Genet Cytogenet 21:179-185.
7. Sandberg AA (1990): The Chromosomes in Human Cancer and Leukemia, 2nd Ed. New York, Elsevier.
8. Hindkjaer J, Hammoudah SAFM, Hansen KB, Jensen PD, Koch J, Peterson B (1995): Translocation (1;16) identified by chromosome painting, and PRimed in situ-labeling (PRINS). Cancer Genet Cytogenet 79:15-20.
9. Pandis N, Heim S, Bardi G, Idvall I, Mandahl N, Mitelman F (1992): Whole-arm t(1;16) and i(1q) as sole anomalies identify gain of 1q as a primary chromosomal abnormality in breast cancer. Genes Chrom Cancer 5:235-238.
10. Mugneret F, Lizard S, Aurius A, Turc-Carel C (1988): Chromosomes in Ewing's sarcoma. II. Nonrandom additional changes, trisomy 8 and der(16)t(1;16). Cancer Genet Cytogenet 32:239-245.
11. Douglass EC, Rowe ST, Valentine M, Parnham D, Meyer WH, Thompson EI (1990): A second non-random translocation der(16)t(1;16)(q21;q13) in Ewing's sarcoma and peripheral neuroectodermal tumor. Cytogenet Cell Genet 53:87-90.
12. Douglass EC, Shapirok DN, Valentine M, Rowe ST (1993): Alveolar rhabdomyosarcoma with the t(2;13): cytogenetic findings and clinicopathologic correlations. Med Pediatr Oncol 21:83-87.
13. Wang-Wuu S, Soukup S, Ballard E, Gotwals B, Lampkin B (1988): Chromosomal analysis of sixteen human rhabdomyosarcomas. Cancer Res 48:983-987.
14. Rowe D, Gerrard M, Gibbons B, Malpas JS (1987): Two further cases of t(2;13) in alveolar rhabdomyosarcoma indicating a review of the published chromosome breakpoints. Br J Cancer 56:379-380.