Malignant transformation of an untreated congenital sacrococcygeal teratoma: a amplification at 8q and 12p detected by comparative genomic hybridization

Cancer Genetics and Cytogenetics

Volumn 197, Issue 1, 2010, Pages 95-98

  Golas, Mariola Monika ^a,b   Gunawan, Bastian ^b,c   Raab, Björn Werner ^b   Füzesi, László ^b   Lange, Bettina ^b,d  

^a AARHUS UNIVERSITY   (Denmark)

^b UNIVERSITY OF GÖTTINGEN   (Germany)

^c Institute of Pathology   (Germany)

^d UNIVERSITY OF HEIDELBERG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CISPLATIN; ETOPOSIDE; IFOSFAMIDE;

ADENOCARCINOMA; ADULT; ANAMNESIS; CANCER COMBINATION CHEMOTHERAPY; CANCER RELAPSE; CASE REPORT; CHROMOSOME 12P; CHROMOSOME 8Q; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; COMPARATIVE GENOMIC HYBRIDIZATION; COMPUTER ASSISTED TOMOGRAPHY; CONGENITAL TUMOR; GENE AMPLIFICATION; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; LETTER; MALE; MALIGNANT TRANSFORMATION; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; SACROCOCCYX TERATOMA; SACROCOCCYX TUMOR;

CELL TRANSFORMATION, NEOPLASTIC; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 12; CHROMOSOMES, HUMAN, PAIR 8; COMPARATIVE GENOMIC HYBRIDIZATION; GENE AMPLIFICATION; HUMANS; MALE; MIDDLE AGED; SACROCOCCYGEAL REGION; TERATOMA;

EID: 74749106744     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cancergencyto.2009.10.013     Document Type: Letter

References (20)

1. Schropp K.P., Lobe T.E., Rao B., Mutabagani K., Kay G.A., Gilchrist B.F., Philippe P.G., and Boles Jr. E.T. Sacrococcygeal teratoma: the experience of four decades. J Pediatr Surg 27 (1992) 1075-1079
2. Biskup W., Calaminus G., Schneider D.T., Leuschner I., and Göbel U. Teratoma with malignant transformation: experiences of the cooperative GPOH protocols MAKEI 83/86/89/96. Klin Padiatr 218 (2006) 303-308
3. Lahdenne P., Heikinheimo M., Nikkanen V., Klemi P., Siimes M.A., and Rapola J. Neonatal benign sacrococcygeal teratoma may recur in adulthood and give rise to malignancy. Cancer 72 (1993) 3727-3731
4. Currarino G., Coln D., and Votteler T. Triad of anorectal, sacral, and presacral anomalies. AJR Am J Roentgenol 137 (1981) 395-398
5. Kuhlgatz J., Sander B., Golas M.M., Gunawan B., Schulze T., Schulten H.J., Wardelmann E., and Füzesi L. Differential diagnosis of gastrointestinal leiomyoma versus gastrointestinal stromal tumor. Int J Colorectal Dis 21 (2006) 84-88
6. Surti U., Hoffner L., Chakravarti A., and Ferrell R.E. Genetics and biology of human ovarian teratomas: I. Cytogenetic analysis and mechanism of origin. Am J Hum Genet 47 (1990) 635-643
7. Bussey K.J., Lawce H.J., Olson S.B., Arthur D.C., Kalousek D.K., Krailo M., Giller R., Heifetz S., Womer R., and Magenis R.E. Chromosome abnormalities of eighty-one pediatric germ cell tumors: sex-, age-, site-, and histopathology-related differences: a Children's Cancer Group study. Genes Chromosomes Cancer 25 (1999) 134-146
8. Mostert M., Rosenberg C., Stoop H., Schuyer M., Timmer A., Oosterhuis W., and Looijenga L. Comparative genomic and in situ hybridization of germ cell tumors of the infantile testis. Lab Invest 80 (2000) 1055-1064
9. van Echten J., Oosterhuis J.W., Looijenga L.H., van de Pol M., Wiersema J., te Meerman G.J., Schaffordt Koops H., Sleijfer D.T., and de Jong B. No recurrent structural abnormalities apart from i(12p) in primary germ cell tumors of the adult testis. Genes Chromosomes Cancer 14 (1995) 133-144
10. Poulos C., Cheng L., Zhang S., Gersell D.J., and Ulbright T.M. Analysis of ovarian teratomas for isochromosome 12p: evidence supporting a dual histogenetic pathway for teratomatous elements. Mod Pathol 19 (2006) 766-771
11. Hoffner L., Deka R., Chakravarti A., and Surti U. Cytogenetics and origins of pediatric germ cell tumors. Cancer Genet Cytogenet 74 (1994) 54-58
12. Noguera R., Navarro S., Carda C., Peydró-Olaya A., and Llombart-Bosch A. Near-haploidy in a malignant sacrococcygeal teratoma. Cancer Genet Cytogenet 108 (1999) 70-74
13. Wax J.R., Benn P., Steinfeld J.D., and Ingardia C.J. Prenatally diagnosed sacrococcygeal teratoma: a unique expression of trisomy 1q. Cancer Genet Cytogenet 117 (2000) 84-86
14. Veltman I., van Asseldonk M., Schepens M., Stoop H., Looijenga L., Wouters C., Govaerts L., Suijkerbuijk R., and van Kessel A. A novel case of infantile sacral teratoma and a constitutional t(12;15)(q13;q25) pat. Cancer Genet Cytogenet 136 (2002) 17-22
15. Veltman I.M., Schepens M.T., Looijenga L.H., Strong L.C., and van Kessel A.G. Germ cell tumours in neonates and infants: a distinct subgroup?. APMIS 111 (2003) 152-160
16. Le Caignec C., Winer N., Boceno M., Delnatte C., Podevin G., Liet J.M., Quere M.P., Joubert M., and Rival J.M. Prenatal diagnosis of sacrococcygeal teratoma with constitutional partial monosomy 7q/trisomy 2p. Prenat Diagn 23 (2003) 981-984
17. Noumoff J.S., LiVolsi V.A., Deger R.B., Montone K.T., and Faruqi S.A. Chromosome analysis and comparison of the benign cystic and malignant squamous component of an ovarian teratoma. Cancer Genet Cytogenet 125 (2001) 59-62
18. De Angelis P.M., Stokke T., Beigi M., Mjåland O., and Clausen O.P. Prognostic significance of recurrent chromosomal aberrations detected by comparative genomic hybridization in sporadic colorectal cancer. Int J Colorectal Dis 16 (2001) 38-45
19. Aragane H., Sakakura C., Nakanishi M., Yasuoka R., Fujita Y., Taniguchi H., Hagiwara A., Yamaguchi T., Abe T., Inazawa J., and Yamagishi H. Chromosomal aberrations in colorectal cancers and liver metastases analyzed by comparative genomic hybridization. Int J Cancer 94 (2001) 623-629
20. He Q.J., Zeng W.F., Sham J.S., Xie D., Yang X.W., Lin H.L., Zhan W.H., Lin F., Zeng S.D., Nie D., Ma L.F., Li C.J., Lu S., and Guan X.Y. Recurrent genetic alterations in 26 colorectal carcinomas and 21 adenomas from Chinese patients. Cancer Genet Cytogenet 144 (2003) 112-118