Juvenile polyposis coli concurrent with neurofibromatosis

Jeffrey B. Raskin, Halbert Dodd

Research output: Contribution to journalArticlepeer-review

8 Scopus citations


Juvenile polyposis coli associated with neurofibromatosis in a 24 year old white man is reported. Juvenile polyposis coli is now recognized as a distinct clinical entity. Differentiating it from the other hereditable gastrointestinal polyposis syndromes is important because of the lack of reported malignancies. Radical surgery is unnecessary unless warranted by the clinical features of bleeding or diarrhea. The known gastrointestinal and extra gastrointestinal associations with juvenile polyposis coli are reviewed along with the gastrointestinal manifestations of neurofibromatosis. This is the first reported association of neurofibromatosis with this unusual syndrome.

Original languageEnglish (US)
Pages (from-to)1374-1376
Number of pages3
JournalSouthern medical journal
Issue number10
StatePublished - Oct 1976

ASJC Scopus subject areas

  • Medicine(all)


Dive into the research topics of 'Juvenile polyposis coli concurrent with neurofibromatosis'. Together they form a unique fingerprint.

Cite this