Skip to main content

Congenital Cancer and Congenital Abnormalities Associated with Cancer

  • Chapter
Hereditary Factors in Carcinoma

Abstract

Malignancies present at birth pose a challenge to the geneticist, embryologist, epidemiologist, and oncologist. One of the most comprehensive reviews of the subject was that of Wells20 in 1940. His criterion for the definite occurrence of a congenital malignancy included the presence of the malignancy at birth and histologic confirmation during the neonatal period. He found about 250 reported congenital neoplasms in the world literature of which only 66 fulfilled this criterion. Sarcoma constituted nearly one-half of all the congenital malignancies while neuroblastoma comprised most of the other half. No convincingly proven cases of congenital carcinoma were found though several “possible” carcinomas were reported (particularly carcinoma of the liver). The proven cases included none of the common malignancies of man, namely lung, alimentary tract, and genitalia.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

eBook
USD 16.99
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 109.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. Bloom, D.: The Syndrome of Congenital Telangiectatic Erythema and Stunted Growth, J. Pediat. 68:103–113, 1966.

    Article  PubMed  CAS  Google Scholar 

  2. Bloom, G. F., Warner, S., Gerald, P. S., and Diamond, L. K.: Chromosome abnormalities in Constitutional Aplastic Anemia, New Eng. J. Med. 274:8–14, 1966.

    Article  PubMed  CAS  Google Scholar 

  3. Dargeon, H. W.: Neuroblastoma, J. Pediat. 61:456-471, 1962.

    Article  PubMed  CAS  Google Scholar 

  4. Ederer, F., Miller, R. W., and Scotto, J.: U.S. Childhood Cancer Mortality Patterns, 1950–1959: Etiologic Implications, JAMA 192: 593–596, 1965.

    Article  PubMed  CAS  Google Scholar 

  5. Fontana, V. J., Ferrara, A., and Perciaccante, R.: Wilms’ Tumor and Associated Anomalies, Amer. J. Dis. Child. 109:459–461, 1965.

    PubMed  CAS  Google Scholar 

  6. Gaulin, E.: Simultaneous Wilms’ Tumors in Identical Twins, J. Urol. 66:547–550, 1951.

    PubMed  CAS  Google Scholar 

  7. Jagasia, K. H. and Thurman, W. G.: Wilms’ Tumor in the Adult, Arch. Intern. Med. 115: 322–325, 1956.

    Article  Google Scholar 

  8. Knudson, A. G. and Amromin, G. D.: Neuroblastoma and Gonglioneuroma in a Child with Multiple Neurofibromatosis, Implication for the Mutational Orgin of Neuroblastoma, Cancer 19: 1032–1037, 1966.

    Article  PubMed  Google Scholar 

  9. Mackay, H.: Congenital Bilateral Megalo-Ureters with Hydronephrosis, Remarkable Family History, Proc. Roy. Soc. Med. 38:546–568, 1945.

    Google Scholar 

  10. Miller, R. W., Fraumani, J. F., Jr., and Manning, M. P.: Association of Wilms’ Tumor with Aniridia, Hemihypertrophy and Other Malformation, New Eng. J. Med. 270:922–927, 1964.

    Article  PubMed  CAS  Google Scholar 

  11. Miller, R. W.: Relation Between Cancer and Congenital Defects in Man, New Eng. J. Med. 275:87–93, 1966.

    Article  PubMed  CAS  Google Scholar 

  12. Potter, E. L. and Parrish, J. M.: Neuroblastoma, Gonglioneuroma, and Fibroneuroma in Stillborn Fetus, Amer. J. Path. 18:141–152, 1952.

    Google Scholar 

  13. Reisman, M., Goldenberg, E. D., and Gordon, J.: Congenital Heart Disease and Neuroblastoma: Case Report and Brief Comment, Amer. J. Dis. Child. 111:308–310, 1956.

    Google Scholar 

  14. Sawitsky, A., Bloom, D., and German, J.: Chromosomal Breakage and Acute Leukemia in Congenital Telangiectatic Erythema and Stunted Growth, Ann. Intern. Med. 65:487–495, 1966.

    PubMed  CAS  Google Scholar 

  15. Schmid, W., Schärer, K., Baumann, T., and Fanconi, G.: Chromomenbruchigkeit bei der familiä;ren Panmylopathie (Typus Fanconi), Schweiz. Med. Wschr. 95:1461–1464, 1965.

    PubMed  CAS  Google Scholar 

  16. Scott, L. S.: Wilms’ Tumor, Diagnosis, Treatment, and Prognosis, Brit. Med. J. 1:200–203, 1956.

    Article  Google Scholar 

  17. Shaw, M. W., Falls, H. F., and Neel, J. V.: Congenital Aniridia, Amer. J. Hum. Genet. 12:389–415, 1960.

    PubMed  CAS  Google Scholar 

  18. Vawter, G. F. and Melvin, T.: Congenital Tumors of the Parotid Gland, Arch. Path. 82:242–245, 1966.

    Google Scholar 

  19. Vinik, M. and Altman, D. H.: Congenital Malignant Tumors, Cancer 19: 967–979, 1966.

    Article  PubMed  CAS  Google Scholar 

  20. Wells, H. G.: Occurrence and Significance of Congenital Malignant Neoplasms, Arch. Path. 30:535–601, 1940.

    Google Scholar 

  21. Wintrobe, M. H.: Clinical Hematology, Philadelphia: Lea and Febiger, 1961.

    Google Scholar 

Download references

Authors

Rights and permissions

Reprints and permissions

Copyright information

© 1967 Springer-Verlag Berlin · Heidelberg

About this chapter

Cite this chapter

Lynch, H.T. (1967). Congenital Cancer and Congenital Abnormalities Associated with Cancer. In: Hereditary Factors in Carcinoma. Recent Results in Cancer Research / Fortschritte der Krebsforschung / Progrès dans les recherches sur le cancer, vol 12. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-48252-6_8

Download citation

  • DOI: https://doi.org/10.1007/978-3-642-48252-6_8

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-642-48254-0

  • Online ISBN: 978-3-642-48252-6

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics