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• W2078525087 abstract "Sacrococcygeal teratomas are frequent congenital neoplasms showing an incidence of approximately 1:35,000–40,000 live births and a female-to-male ratio of approximately 4:1 [ [1] Schropp K.P. Lobe T.E. Rao B. Mutabagani K. Kay G.A. Gilchrist B.F. Philippe P.G. Boles Jr., E.T. Sacrococcygeal teratoma: the experience of four decades. J Pediatr Surg. 1992; 27: 1075-1079 Abstract Full Text PDF PubMed Scopus (122) Google Scholar ]. Malignant transformation has been found in approximately 1% of teratoma patients [ [2] Biskup W. Calaminus G. Schneider D.T. Leuschner I. Göbel U. Teratoma with malignant transformation: experiences of the cooperative GPOH protocols MAKEI 83/86/89/96. Klin Padiatr. 2006; 218: 303-308 Crossref PubMed Scopus (39) Google Scholar ], frequently comprising squamous cell carcinoma, but also adenocarcinomas, sarcomas, and other malignancies. Thus, teratomas are suggested to be regarded as tumors with malignant potential, which calls for accurate treatment and long-term follow-up [ [3] Lahdenne P. Heikinheimo M. Nikkanen V. Klemi P. Siimes M.A. Rapola J. Neonatal benign sacrococcygeal teratoma may recur in adulthood and give rise to malignancy. Cancer. 1993; 72: 3727-3731 Crossref PubMed Scopus (22) Google Scholar ]. Little is known about untreated teratomas." @default.
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• W2078525087 date "2010-02-01" @default.
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• W2078525087 title "Malignant transformation of an untreated congenital sacrococcygeal teratoma: a amplification at 8q and 12p detected by comparative genomic hybridization" @default.
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• W2078525087 doi "https://doi.org/10.1016/j.cancergencyto.2009.10.013" @default.
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