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Original Article

Familial Adenomatous Polyposis Coli and Clear Cell Sarcoma of the Kidney

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Pages 133-141 | Received 14 Aug 1992, Accepted 14 Sep 1992, Published online: 09 Jul 2009

References

  • Bodmer W F, Bailey C, Bodmer J, et al. Localization of the gene for familial adenomatous polyposis on chromosome 5. Nature 1987; 328: 614–6
  • Bussey H JR. Familial Polyposis Coli: Family Studies, Histopathology, Differential Diagnosis, and Results of Treatment. Johns Hopkins University Press, Baltimore 1975
  • Cohen S B. Familial polyposis coli and its extracolonic manifestations. J Med Genet 1982; 19: 193–203
  • Gardner E J. Follow up study of a family group exhibiting dominant inheritance for a syndrome including intestinal polyps, osteomas, fibromas and epidermal cysts. Am J Genet Hum 1962; 14: 376–90
  • Turcot J, Despres J P, St Pierre F. Malignant tumors of the central nervous system associated with familial polyposis of the colon. Dis Colon Rectum 1959; 2: 465–8
  • Kingston J E, Herbert A, Draper G J, Mann J R. Association between hepatoblastoma and polyposis coli. Arch Dis Child 1983; 58: 959–62
  • Watanabe H, Enjoji M, Yao T, et al. Gastric lesions in familial adenomatous coli. Their incidence and histologic analysis. Hum Pathol 1978; 9: 269–83
  • Schneider N R, Cubilla A L, Changanti R SK. Association of endocrine neoplasia with familial multiple colon polyps. Am J Hum Genet 1980; 32: 128A
  • Perkins J T, Blackstone M O, Riddell R H. Adenomatous polyposis coli and multiple endocrine neoplasm type 2b. Cancer 1985; 55: 375–81
  • Knudson A G, Jr. Hereditary cancer, oncogenes, and antioncogenes. Cancer Res 1985; 45: 1473–43
  • Li F P, Fraumeni J F, Jr. Soft tissue sarcomas, breast cancer, and other neoplasms: A familial syndrome. Am Intern Med 1969; 71: 747–52
  • Wiggs J, Nordenskjold M, Yandell D, et al. Prediction of the risk of hereditary retinoblastoma using DNA polymorphisms within the retinoblastoma gene. N Engl J Med 1988; 318: 151–7
  • Sotelo-Avila C, Gonzalez-Crussi F, Fowler J W. Complete and incomplete forms of Beckwith-Wiedemann syndrome: Their oncogenic potential. J Pediatr 1980; 96: 47–50
  • Miller R W, Fraumeni J F, Jr, Manning M D. Association of Wilms' tumor with aniridia hemihy-pertrophy and other congenital malformations. N Engl J Med 1964; 270: 922–7
  • Herrera L, Kakati S, Gibas L, Pietrzak E, Sandberg A. Brief clinical report: Gardner syndrome in a man with an interstitial deletion of 5q. Am J Med Genet 1986; 25: 473–6
  • Vogelstein B, Fearon E, Hamilton S, et al. Genetic alterations during colorectal tumor development. N Engl J Med 1988; 319: 525–32
  • Joslyn G, Carlson M, Thliveris A, et al. Identification of deletion mutations and three new genes at the familial polyposis locus. Cell 1991; 66: 601–13
  • Groden J, Thliveris A, Samowitz W, et al. Identification and characterization of the familial adenomatous polyposis coli gene. Cell 1991; 66: 589–600
  • Beckwith J B. Wilms' tumor and other renal tumors of childhood: A selective review from the National Wilms' Tumor Study Pathology Center. Hum Pathol 1983; 14: 481–92
  • Marsden H B, Lawler W, Kumar P M. Bone metastasizing renal tumor of childhood. Morphological and clinical features and differences from Wilms' tumor. Cancer 1978; 42: 1922–28
  • Punnett H H, Halligan G E, Zaeri N, Karmazin N. Translocation 10; 17 in clear cell sarcoma of the kidney. A first report. Cancer Genet Cytogenet 1989; 41: 123–8
  • Yoshida M A, Ikeuchi T, Iwama T, et al. Chromosome changes in desmoid tumors developed in patients with familial adenomatous polyposis. Jpn J Cancer Res 1991; 82: 916–21
  • Akira H, Nakatsuru S, Miyoshi Y, et al. The APC gene responsible for familial adenomatous polyposis is mutated in human gastric cancer. Cancer Res 1992; 52: 3231–3
  • Takai S, Iwama T, Tonomura A. Chromosome instability in cultured skin fibroblasts from patients with familial polyposis coli and Peutz-Jeghers' syndrome. Jpn J Cancer Res 1986; 77: 759–66
  • Marczynska B, Hoijer J, Spragia L, et al. Chromosomal and c-K-ras oncogene alterations induced by a chemical carcinogen and phorbol esters in skin fibroblasts of individuals with familial polyposis coli. Carcinogenesis 1988; 9: 1897–1900
  • Lebo R V, Conneally P M, Flandermeyer R R, . The multilocus Charcot-Marie-Tooth syndrome. Charcot-Marie-Tooth Disorders: Pathophysiology, Molecular Genetics and Therapy, A Liss, et al. Alan R. Liss, New York 1990; 307–34
  • Prockop D J, Olsen A, Kontusaari S, et al. Mutations in human procollagen genes: Consequences of the mutations in man and in transgenic mice. Ann NY Acad Sci 1990; 580: 330–9

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