Malignant peripheral nerve sheath tumor with rhabdomyoblastic differentiation (malignant triton tumor) with balanced t(7;9)(q11.2;p24) and unbalanced translocation der(16)t(1;16)(q23;q13)

Cancer Genetics and Cytogenetics

Volumn 149, Issue 1, 2004, Pages 23-27

  Velagaleti, Gopalrao V N ^a   Miettinen, Markku ^b   Gatalica, Zoran ^c  

^a UNIVERSITY OF TEXAS MEDICAL BRANCH   (United States)

^b ARMED FORCES INSTITUTE OF PATHOLOGY   (United States)

^c CREIGHTON UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ANAMNESIS; CANCER PATIENT; CASE REPORT; CHROMOSOME; CHROMOSOME 1; CHROMOSOME 16; CHROMOSOME 7; CHROMOSOME 7Q; CHROMOSOME 9; CHROMOSOME 9P; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION; HISTOPATHOLOGY; HUMAN; IMMUNOHISTOCHEMISTRY; IMMUNOPHENOTYPING; MALE; MALIGNANT TRITON TUMOR; MICROSCOPY; MONOSOMY; MUSCLE DEVELOPMENT; NERVE SHEATH TUMOR; NEUROFIBROMATOSIS; OUTCOMES RESEARCH; PRIORITY JOURNAL; PROGNOSIS; REVIEW; SARCOMA; SKELETAL MUSCLE; TRISOMY; TUMOR VOLUME;

EID: 0842324412     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(03)00278-4     Document Type: Article

References (37)

1. Weiss S.W., Goldblum J.R. Enzinger and Weiss's soft tissue tumors. 4th edition :2001;Mosby, St. Louis.
2. Mertens F., Strömberg, Mandahl N., Dal Cin P., De Wever I., Fletcher C.D.M., Mitelman F., Rosai J., Rydholm A., Sciot R., Tallini G., Van den Berghe H., Vanni R., Willen H. Prognostically important chromosomal aberrations in soft tissue sarcomas: a report of the chromosome and morphology (CHAMP) study group. Cancer Res. 62:2002;3980-3984.
3. Becher R., Wake N., Gibas Z., Ochi H., Sandberg A.A. Chromosome changes in soft tissue sarcomas. J Natl Cancer Inst. 72:1984;823-831.
4. Riccardi V.M., Elder D.W. Multiple cytogenetic aberrations in neurofibrosarcomas complicating neurofibromatosis. Cancer Genet Cytogenet. 23:1986;199-209.
5. Decker H.J., Cannizzaro L.A., Mendez M.J., Leong S.P.L., Bixenman H., Berger C., Sandberg A.A. Chromosomes 17 and 22 involved in marker formation in neurofibrosarcoma in von Recklinghausen disease. Hum Genet. 85:1990;337-342.
6. Fletcher J.A., Kozakewich H.P., Hoffer F.A., Lage J.M., Weidner N., Tepper R., Pinkus G.S., Morton C.C., Corson J.M. Diagnostic relevance of clonal cytogenetic aberrations in malignant soft-tissue tumors. N Engl J Med. 324:1991;436-442.
7. Glover T.W., Stein C.K., Legius E., Andersen L.B., Brereton A., Johnson S. Molecular and cytogenetic analysis of tumors in von Recklinghausen neurofibromatosis. Genes Chromosomes Cancer. 3:1991;62-70.
8. Valdueza J.M., Hagel C., Westphal M., Hansel M., Herrmann H.D. Primary spinal malignant schwannoma: clinical histological and cytogenetic findings. Neurosurg Rev. 14:1991;283-291.
9. Bello M.J., de Campos J.M., Kusak M.E., Vaquero J., Sarasa J.L., Pestana A., Rey J.A. Clonal chromosome aberrations in neurinomas. Genes Chromosomes Cancer. 6:1993;206-211.
10. Neumann E., Kalousek D.A., Norman M.G., Steinbok P., Cochrane D.D., Goddard K. Cytogenetic analysis of 109 pediatric central nervous system tumors. Cancer Genet Cytogenet. 71:1993;40-49.
11. Rey J.A., Bello M.J., Kusak M.E., Camposde J.M., Pestana A. Involvement of 22q12 in a neurofibrosarcoma in neurofibromatosis type I. Cancer Genet Cytogenet. 66:1993;28-32.
12. Jhanwar S.C., Chen Q., Li F.P., Brennan M.F., Woodruff J.M. Cytogenetic analysis of soft tissue sarcomas: recurrent chromosome abnormalities in malignant peripheral nerve sheath tumors (MPNST). Cancer Genet Cytogenet. 78:1994;138-144.
13. Travis J.A., Sandberg A.A., Neff J.R., Bridge J.A. Cytogenetic findings in malignant triton tumor. Genes Chromosomes Cancer. 9:1994;1-7.
14. Mertens F., Heim S., Kullendorff C.M., Donner M., Hagerstrand I., Mitelman F., Mandahl N. Clonal karyotypic evolution in a pediatric neurofibrosarcoma. Cancer Genet Cytogenet. 81:1995;135-138.
15. Mertens F., Rydholm A., Bauer H.F., Limon J., Nedoszytiko B., Szadowska A., Willen H., Heim S., Mitelman F., Mandahl N. Cytogenetic findings in malignant peripheral nerve sheath tumors. Int J Cancer. 61:1995;793-798.
16. Sciot R., Dal Cin P., Fletcher C.D., de Wever I., de Vos R., van Damme B., van den Berghe H. Monosomy 22 in a malignant peripheral nerve sheath tumor of the kidney in childhood: a genetic link with other malignant paediatric renal neoplasms? Histopathology. 27:1995;373-376.
17. McComb E.N., McComb R.D., DeBoner J.M., Neff J.R., Bridge J.A. Cytogenetic analysis of a malignant triton tumor and a malignant peripheral nerve sheath tumor and a review of literature. Cancer Genet Cytogenet. 91:1996;8-12.
18. Rao U.N.M., Surti U., Hoffner L., Yaw K. Cytogenetic and histologic correlation of peripheral nerve sheath tumors of soft tissue. Cancer Genet Cytogenet. 88:1996;8-12.
19. Lothe R.A., Karhu R., Mandahl N., Mertens F., Saeter G., Heim S., Borresen-Dale A.L., Kallioniemi O.P. Gain of 17q24-qter detected by comparative genomic hybridization in malignant tumors from patients with von Recklinghausen's neurofibromatosis. Cancer Res. 56:1996;4778-4781.
20. Pauwels P., Dal Cin P., Sciot R., Lammens M., Penn O., van Nes E., Kwee W.S., van den Berghe H. Primary malignant peripheral nerve sheath tumor of the heart. Histopathology. 34:1999;56-59.
21. Plaat B.E.C., Molenaar W.M., Mastik M.F., Hoekstra H.J., te Meerman G.J., van den Berg E. Computer-assisted cytogenetic analysis of 51 malignant peripheral nerve sheath tumors: sporadic vs neurofibromatosis-type I-associated malignant schwannomas. Int J Cancer. 83:1999;171-178.
22. Hennig Y., Löschke S., Katenkamp D., Bartnitzke S., Bullerdiek J. A malignant triton tumor with an unbalanced translocation (1;13) (q10;q10) and an isochromosome (8)(q10) as the sole karyotypic abnormalities. Cancer Genet Cytogenet. 118:2000;80-82.
23. Schmidt H., Taubert H., Wurl P., Bache M., Bartel F., Holzhausen H.J., Hinze R. Cytogenetic characterization of six malignant peripheral nerve sheath tumors: comparison of karyotyping and comparative genomic hybridization. Cancer Genet Cytogenet. 128:2001;14-23.
24. Haddadin M.H., Hawkins A.L., Long P., Morsberger L.A., Depew D., Epstein J.I., Griffin C.A. Cytogenetic study of malignant triton tumor: a case report. Cancer Genet Cytogenet. 144:2003;100-105.
25. Trojani M., Contesso G., Coindre J.M., Rouesse J., Bui N.B., de Mascarel A., Goussot J.F., David M., Bonichon F., Lagarde C. Soft tissue sarcomas of adults: study of pathological prognostic variables and definition of histopathologic grading system. Int J Cancer. 33:1984;37-42.
26. Sovani V., Velagaleti G.V.N., Filipowicz E., Gatalica Z., Knisely A.S. Ossifying fibromyxoid tumor of soft parts: report of a case with novel cytogenetic findings. Cancer Genet Cytogenet. 127:2001;1-6.
27. Pearson P. The use of new staining techniques for human chromosome identification. J Med Genet. 9:1972;264-275.
28. Mitelman F. An international system for human cytogenetic nomenclature. 1995;S. Karger, Basel.
29. Takeda O., Homma C., Maseki N., Sakurai M., Kanda N., Schwab M., Nakamura Y., Kaneko Y. There may be two tumor suppressor genes on chromosome arm 1p closely associated with biologically distinct subtypes of neuroblastoma. Genes Chromosomes Cancer. 10:1994;30-39.
30. Schleiermacher G., Peter M., Michon J., Hugot J.P., Vielh P., Zucker J.M., Magdelenat H., Thomas G., Delattre O. Two distinct deleted regions on the short arm of chromosome 1 in neuroblastoma. Genes Chromosomes Cancer. 10:1994;275-281.
31. Meza-Zepeda L.A., Forus A., Lygren B., Dahlberg A.B., Godager L.H., South A.P., Marenholz I., Lioumi M., Florenes V.A., Maelandsmo G.M., Serra M., Mischke D., Nizetic D., Ragoussis J., Tarkkanen M., Nesland J.M., Knuutila S., Myklebost O. Positional cloning identifies a novel cyclophilin as a candidate amplified oncogene in 1q21. Oncogene. 21:2002;2261-2269.
32. Le Baccon P., Leroux D., Dascalescu C., Duley S., Marais D., Esmenjaud E., Sotto J.J., Callanan M. Novel evidence of a role for chromosome 1 pericentromeric heterochromatin in the pathogenesis of B-cell lymphoma and multiple myeloma. Genes Chromosomes Cancer. 32:2001;250-264.
33. Forus A., Berner J.M., Meza-Zepeda L.A., Saeter G., Mischke D., Fodstad O., Myklebost O. Molecular characterization of a novel amplicon at 1q21-q22 frequently observed in human sarcomas. Br J Cancer. 78:1998;495-503.
34. Zhang J., Glatfelter A.A., Taetle R., Trent J.M. Frequent alterations of evolutionary conserved regions of chromosomes 1 in human malignant melanoma. Cancer Genet Cytogenet. 111:1999;119-123.
35. McManus A.P., Min T., Swansbury G.J., Gusterson B.A., Pinkerton C.R., Shipley J.M. der(16)t(1;16)(q21;q13) as a secondary change in alveolar rhadbomyosarcoma: a case report and review of the literature. Cancer Genet Cytogenet. 87:1996;179-181.
36. Demetrick D.J., Zhang H., Beach D.H. Chromosomal mapping of genes for human CDK2 cyclin A-associated proteins p19 (SKP1A and SKP1B) and p45 (SKP2). Cytogenet Cell Genet. 73:1996;104-107.
37. Kim S.K., Ro J.Y., Kemp B.L., Lee J.S., Kwon T.J., Fong K.M., Sekido Y., Minna J.D., Hong W.K., Mao L. Identification of three distinct tumor suppressor loci on the short arm of chromosome 9 in small cell lung cancer. Cancer Res. 57:1997;400-403.