Literature DB >> 21614588

The liver: another organ involved in Muir Torre syndrome?

F Morando1, M Alaibac, A Romano, M Cavallin, S Piano, M Pizzi, C Mescoli, P Pilati, A Gatta, P Angeli.   

Abstract

Muir Torre syndrome is a rare autosomal dominant cancer-predisposing syndrome characterized by the occurrence of sebaceous gland neoplasms and/or keratoacanthomas associated with visceral malignancies that belong to the spectrum of hereditary non polyposis colorectal cancer (HNPCC), i.e., tumors of gastrointestinal and genitourinary tracts. Hepatobiliary malignancy in association with Muir Torre syndrome has rarely been reported. Here, we describe a case of Muir Torre syndrome associated with an hepatocellular-carcinoma in a patient with a non-cirrhotic liver and an HNPCC-family with multiple cases of hepatocellular carcinoma.

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Year:  2012        PMID: 21614588     DOI: 10.1007/s10689-011-9450-1

Source DB:  PubMed          Journal:  Fam Cancer        ISSN: 1389-9600            Impact factor:   2.375


  29 in total

1.  Switching from tacrolimus to sirolimus halts the appearance of new sebaceous neoplasms in Muir-Torre syndrome.

Authors:  Z Levi; R Hazazi; I Kedar-Barnes; E Hodak; E Gal; E Mor; Y Niv; J Winkler
Journal:  Am J Transplant       Date:  2007-01-04       Impact factor: 8.086

2.  Attenuated familial adenomatous polyposis and Muir-Torre syndrome linked to compound biallelic constitutional MYH gene mutations.

Authors:  G Ponti; M Ponz de Leon; S Maffei; M Pedroni; L Losi; C Di Gregorio; V Gismondi; A Scarselli; P Benatti; B Roncari; S Seidenari; G Pellacani; C Varotti; E Prete; L Varesco; L Roncucci
Journal:  Clin Genet       Date:  2005-11       Impact factor: 4.438

3.  Drinking habits as cofactors of risk for alcohol induced liver damage. The Dionysos Study Group.

Authors:  S Bellentani; G Saccoccio; G Costa; C Tiribelli; F Manenti; M Sodde; L Saveria Crocè; F Sasso; G Pozzato; G Cristianini; G Brandi
Journal:  Gut       Date:  1997-12       Impact factor: 23.059

4.  Multiple sebaceous tumors.

Authors:  D Torre
Journal:  Arch Dermatol       Date:  1968-11

5.  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

6.  New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC.

Authors:  H F Vasen; P Watson; J P Mecklin; H T Lynch
Journal:  Gastroenterology       Date:  1999-06       Impact factor: 22.682

7.  Microsatellite instability mutator phenotype in hepatocellular carcinoma in non-alcoholic and non-virally infected normal livers.

Authors:  Franck Chiappini; Marine Gross-Goupil; Raphaël Saffroy; Daniel Azoulay; Jean-François Emile; Luc-Antoine Veillhan; Valérie Delvart; Stephan Chevalier; Henri Bismuth; Brigitte Debuire; Antoinette Lemoine
Journal:  Carcinogenesis       Date:  2003-12-04       Impact factor: 4.944

8.  Sebaceous neoplasia and Torre-Muir syndrome.

Authors:  A J F Lazar; S Lyle; E Calonje
Journal:  Curr Diagn Pathol       Date:  2007-08

9.  Genetic instability in pancreatic cancer and poorly differentiated type of gastric cancer.

Authors:  H J Han; A Yanagisawa; Y Kato; J G Park; Y Nakamura
Journal:  Cancer Res       Date:  1993-11-01       Impact factor: 12.701

10.  Microsatellite instability in Muir-Torre syndrome.

Authors:  R Honchel; K C Halling; D J Schaid; M Pittelkow; S N Thibodeau
Journal:  Cancer Res       Date:  1994-03-01       Impact factor: 12.701

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