Literature DB >> 1156682

Cowden disease.

W C Gentry, W B Reed, J M Siegel.   

Abstract

Cowden disease represents an unusual, but unique syndrome which can be recognized most consistently by the development of characteristic verrucous, keratotic, papular, and nodular lesions about facial orifices, on the oral mucosa, and over the dorsal surfaces of the forearms and hands. The cause of these diverse hyperplastic changes is not known. Recognition of these lesions as signs of more extensive disease should alert the physician to examine the thyroid gland, breasts, female reproductive tract, GI tract, and skeleton for evidence of the associated changes we have enumerated. Because of the tendency for lesions of the thyroid, breast, and intestines to undergo malignant change, these patients require close observation and evaluation.

Entities:  

Mesh:

Year:  1975        PMID: 1156682

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN: 0547-6844


  3 in total

Review 1.  Cowden's disease: a case report and literature review.

Authors:  Y M Chen; D J Ott; W C Wu; D W Gelfand
Journal:  Gastrointest Radiol       Date:  1987

2.  Cowden's disease: familial goiter and skin hamartomas. A report of three cases.

Authors:  P B Sogol; M Sugawara; H E Gordon; W V Shellow; F Hernandez; J M Hershman
Journal:  West J Med       Date:  1983-09

3.  Association of multinodular goiter with breast carcinoma: Cowden's disease.

Authors:  R D Michaels; K M Shakir
Journal:  J Endocrinol Invest       Date:  1993-12       Impact factor: 4.256

  3 in total

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