Literature DB >> 16455548

Cowden's syndrome with Lhermitte-Duclos disease.

T Boonpipattanapong1, N Phuenpathom, W Mitarnun.   

Abstract

Cowden's syndrome (CS) is a rare autosomal dominant condition featuring multiple hamartomas, often with mucocutaneous lesions, goitre, breast cancer, gastrointestinal polyps or even Lhermitte-Duclos disease (LDD). In this article we report the case of a 34-year-old man who was diagnosed with LDD. Subsequent examinations also revealed manifestations of CS, i.e. macrocephaly, thyroid nodules and gastrointestinal polyps.

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Year:  2005        PMID: 16455548     DOI: 10.1080/02688690500305431

Source DB:  PubMed          Journal:  Br J Neurosurg        ISSN: 0268-8697            Impact factor:   1.596


  2 in total

1.  Lhermitte Duclos disease: a rare cause of posterior fossa mass.

Authors:  Kenneth D Katz; Andrew G Bleicher; Julia K Kofler
Journal:  Intern Emerg Med       Date:  2008-02-15       Impact factor: 3.397

2.  Lhermitte-Duclos disease: A rare entity.

Authors:  J K Bhatia; H S Bhatoe; Shashi Vadhanan
Journal:  Med J Armed Forces India       Date:  2016-05-06
  2 in total

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