Nasopharyngeal angiofibroma in patients with familial adenomatous polyposis

Francis M. Giardiello, Stanley R. Hamilton, Anne J. Krush, Johan A. Offerhaus, Susan V. Booker, Gloria M. Petersen

Research output: Contribution to journalArticle

62 Scopus citations

Abstract

Four patients with nasopharyngeal angiofibroma and familial adenomatous polyposis are reported here. Nasopharyngeal angiofibroma was 25 times more frequent in our patient population with familial adenomatous polyposis than in an age-matched hospital population. The association of these two rare conditions suggests that nasopharyngeal angiofibroma is an extracolonic manifestation of adenomatous polyposis. In addition, somatic mutation of the adenomatous polyposis coll gene, which causes adenomatous polyposis when mutated in the germline, could play a role in the pathogenesis of sporadic nasopharyngeal angiofibroma.

Original languageEnglish (US)
Pages (from-to)1550-1552
Number of pages3
JournalGastroenterology
Volume105
Issue number5
DOIs
StatePublished - Nov 1993

ASJC Scopus subject areas

  • Hepatology
  • Gastroenterology

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    Giardiello, F. M., Hamilton, S. R., Krush, A. J., Offerhaus, J. A., Booker, S. V., & Petersen, G. M. (1993). Nasopharyngeal angiofibroma in patients with familial adenomatous polyposis. Gastroenterology, 105(5), 1550-1552. https://doi.org/10.1016/0016-5085(93)90164-8