References
- Hartley A L, Birch J M, Kelsey A M, Jones M, Harris M, Blair V. Epidemiologie and familial aspects of hepatoblastoma. Med Pediatr Oncol 1990; 18: 103–9
- Weinberg A, Finegold M J. Primary hepatic tumors in childhood. Pathology of Neoplasia in Children and Adolescents. Vol. 18. Major Problems in Pathology, M Finegold. W. B. Sannders, Philadelphia 1986; 333–43
- Lack E E, Neave C, Vawter G F. Hepatoblastoma. A clinical and pathologic study of 54 cases. Am J Snrg Pathol 1982; 6: 693–705
- Haas J E, Muczynski K A, Krailo M, et al. Histopathology and prognosis in childhood hepatoblastoma and hepatocarcinoma. Cancer 1989; 65: 1092–5
- Ishak K G, Glnnz P R. Hepatoblastoma and hepatocarcinoma in infancy and childhood. Cancer 1967; 20: 396–422
- Benjamin E, Lendon M. Marsden HB. Hepatoblastoma as a cause of intrauterine fetal death—case report. Br Obstet Gynaecol 1981; 88: 329–32
- Napoli V M, Campbell W G. Hepatoblastoma in infant sister and brother. Cancer 1977; 39: 2647–50
- Fraumeni J F, Miller R W, Hill J A. Primary carcinoma in the liver in childhood: An epidemiologic study. J Natl Cancer Inst 1968; 40: 1087–97
- Koufos A, Hansen M F, Copeland N G, Jenkins N A, Lampkin B C, Cavenee W K. Loss of heterozygosity in three embryonal tumours suggest a common pathogenic mechanism. Nature 1985; 316: 330–4
- Haas O A, Zoubek A, Grumayer E R, Gadner H. Constitutional interstitial deletion of 11p11 and pericentric inversion of chromosome 9 in a patient with Wiedemann-Beckwith syndrome and hepatoblastoma. Cancer Genet Cytogenet 1986; 23: 95–104
- Smith's Recognizable Patterns of Human Malformation: Volume VII, in the series Major problems in clinical pediatrics. 4th ed., K L Jones. W. B. Saunders, Philadelphia 1988; 136–9
- Kubota T, Saitoh S, Matsumoto T, et al. Excess functional copy of allele at chromosomal region 11p15 may cause Wiedemann-Beckwith (EMG) syndrome. Am J Med Genet 1994; 49: 378–83
- Kingston J E, Herbert A, Draper G J, Mann J R. Association between hepatoblastoma and polyposis coli. Arch Dis Child 1983; 58: 959–62
- Li F P, Thurber W A, Seddon J, Holmes G E. Hepatoblastoma in families with polyposis coli. JAMA 1987; 257: 2475–7
- Phillips M, Dicks-Mireaux C, Kingston J, et al. Hepatoblastoma and polyposis coli (familial adenomatous polyposis). Med Pediatr Oncol 1989; 17: 441–7
- Wang-Wuu S, Soukup S, Bove K, Gotwals B, Lampkin B. Chromosome analysis of 31 Wilms' tumors. Cancer Res 1990; 50: 2786–93
- Root S, Carey J C. Survival in trisomy 18. Am J Med Genet 1994; 49: 170–4
- Robinson M G, McQuorquodale M M. Trisomy 18 and neurogenic neoplasia. J Pediatr 1981; 99: 428–9
- Geiser C F, Schindler A M. Long survival in a male with trisomy 18 and Wilms tumor. Pediatrics 1969; 44: 111–5
- Karayalcin G, Shanske A, Honigman R. Wilms' tumor in a 13 year old girl with trisomy 18. Am J Dis Child 1981; 135: 665–7
- Faucette K J, Carey J C, Lemons R L, Toledano S. Trisomy 18 and Wilms tumor. Is there an association?. Clin Res 1991; 39: 96A
- Dasouki M, Barr M, Jr. Brief clinical report: Trisomy 18 and hepatic neoplasia. Am J Med Genet 1987; 27: 203–5
- Mamlok V, Nichols M, Lockhart L, Mamlok R. Trisomy 18 and hepatoblastoma. Am J Med Genet 1989; 33: 125–6
- Tanaka K, Uemolo S, Asonuma K, et al. Hepatoblastoma in a 2-year-old girl with trisomy 18. Eur J Pediatr Surg 1992; 2: 298–300
- Lisch Z. Trisomy 1993; 15: 16–17, 13/18 Newsletter Spring/Summer
- Warkany J, Passarge E, Smith L P. Congenital malformations in autosomal trisomy syndromes. Am J Dis Child 1969; 112: 502–17
- Smith D W. Recognizable Patterns of Human Malformation. Genetic, Embryologie and Clinical Aspects. Volume VII in the series Major Problems in Clinical Pediatrics. 3rd ed. W. B. Saunders, Philadelphia 1982; 14–17
- Human Malformation and Related Anomalies, R E Stevenson, J G Hall, R M Goodman. Oxford University Press, Oxford 1993; Vol. II: 450–52
- Bolande R P. Prenatal carcinogenesis. An appraisal. Cancer 1994; 74: 1674–93
- Marois D, van Heerden J A, Carpenter H A, Sheedy P F. Congenital absence of the portal vein. Mayo Clin Proc 1979; 54: 55–9
- Barton J W, Keller M S. Liver transplantation for hepatoblastoma in a child with congenital absence of the portal vein. Pediatr Radiol 1990; 20: 113–4
- Hedbord F, Holmgren L, Sandstedt B, Ohlsson R. The cell type-specific IGF2 expression during early human development correlates to the pattern of overgrowth and neoplasia in the Beckwith-Wiedemann syndrome. Am J Pathol 1994; 145: 802–17
- Bove K E, Koffler H, McAdams A J. Nodular renal blastema, definition and possible significance. Cancer 1969; 24: 323–32
- Shanklin D R, Sotelo-Avila C. In situ tumors in fetuses, newborns and infants. Biol Neonate 1969; 14: 286–316
- Bove K E, Kiser-Debrosse B, Lewis C. Proliferation and maturation indices in nephrogenic rests and Wilms tumor: The emergence of heterogencity from dormant nodular renal blastema. Pediatr Pathol. & Lab Med 1995; 15: 223–44
- Fletcher J A, Kozakewich H P, Pavelka K, et al. Consistent cytogenetic aberrations in hepatoblastoma: A common pathway of genetic alterations in embryonal liver and skeletal muscle malignancies?. Genes Chromosom Cancer 1991; 3: 37–43
- Bardi G, Johansson B, Pandix N, et al. Trisomy 2 as the sole chromosomal abnormality in a hepatoblastoma. Genes Chromosom Cancer 1992; 4: 178–80
- Tonk V S, Wilson K S, Timmons C F, Schneider N R. Trisomy 2, trisomy 20, and del (17p) as sole chromosomal abnormalities in three cases of hepatoblastoma. Genes Chromosom Cancer 1994; 11: 199–202
- Wolman S R. Cytogenetic heterogeneity: Its role in tumor evolution. Cancer Genet Cytogenet 1986; 19: 129–40