Literature DB >> 18990276

Muir-Torre syndrome: a case report and screening recommendations.

A Pancholi1, D Collins, R Lindley, P Gandhi.   

Abstract

Muir-Torre syndrome is a rare genodermatosis (hereditary cancer syndrome associated with distinguishing cutaneous signs) characterised by occurrence of sebaceous neoplasia and visceral malignancy. Colorectal cancer is the commonest visceral malignancy associated with Muir-Torre syndrome. We discuss a case report along with recommendations for diagnosis and screening.

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Year:  2008        PMID： 18990276      PMCID： PMC2727817          DOI： 10.1308/147870808X360387

Source DB:  PubMed          Journal:  Ann R Coll Surg Engl        ISSN： 0035-8843            Impact factor:   1.891


  4 in total

1.  Muir-Torre syndrome.

Authors:  J Coldron; I Reid
Journal:  J R Coll Surg Edinb       Date:  2001-06

Review 2.  Muir-Torre syndrome: case report of a patient with concurrent jejunal and ureteral cancer and a review of the literature.

Authors:  S Akhtar; K K Oza; S A Khan; J Wright
Journal:  J Am Acad Dermatol       Date:  1999-11       Impact factor: 11.527

3.  Multiple primary carcinomata of the colon, duodenum, and larynx associated with kerato-acanthomata of the face.

Authors:  E G Muir; A J Bell; K A Barlow
Journal:  Br J Surg       Date:  1967-03       Impact factor: 6.939

4.  Muir-Torre syndrome: Diagnostic and screening guidelines.

Authors:  Brad Jones; Carol Oh; Elisabeth Mangold; Conleth A Egan
Journal:  Australas J Dermatol       Date:  2006-11       Impact factor: 2.875
  4 in total
  1 in total

1.  Generational Expression of Muir-Torre Syndrome in a Canadian Family.

Authors:  Kaitlin Alexandra Vanderbeck; R Gary Sibbald; Nirosha Murugan
Journal:  Case Rep Dermatol Med       Date:  2016-10-16
  1 in total

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