Abstract
Distinctive cutaneous lesions frequently accompany and occasionally precede the intestinal lesions in Gardner's syndrome, Peutz-Jeghers syndrome, and Muir's syndrome. Awareness of the dermatologic manifestations of these entities may facilitate early diagnosis in these potentially life-threatening hereditary disorders.
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References
Smith WG. Desmoid tumors in familial multiple polyposis. Mayo Clin Proc 1959;34:31–8.
Utsunomiya J, Gocho H, Miyanaga T, et al. Peutz-Jeghers syndrome: its natural course and management. Johns Hopkins Med J 1975;136:71–82.
Housholder MS, Zeligman I. Sebaceous neoplasms associated with visceral carcinomas. Arch Dermatol 1990;116:61–4.
Anderson DE. An inherited form of large bowel cancer: Muir's syndrome. Cancer 1980;45:1103–4.
Veale AM. Intestinal polyposis, Eugenics Laboratory Memoirs XL, Galton Laboratory, London: Cambridge University Press 1965: 104.
Goodman ZD, Yardley JH, Milligan FD. Pathogenesis of colonic polyps in multiple juvenile polyposis: report of a case associated with gastric polyps and carcinoma of the rectum. Cancer 1979;43:1906–13.
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Hood, A.B., Krush, A.J. Clinical and dermatologic aspects of the hereditary intestinal polyposes. Dis Colon Rectum 26, 546–548 (1983). https://doi.org/10.1007/BF02563753
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DOI: https://doi.org/10.1007/BF02563753