Literature DB >> 29196359

Inherited skin tumour syndromes.

Sarah Brown1, Paul Brennan1, Neil Rajan1.   

Abstract

This article provides an overview of selected genetic skin conditions where multiple inherited cutaneous tumours are a central feature. Skin tumours that arise from skin structures such as hair, sweat glands and sebaceous glands are called skin appendage tumours. These tumours are uncommon, but can have important implications for patient care. Certain appendageal tumours, particularly when multiple lesions are seen, may indicate an underlying genetic condition. These tumours may not display clinical features that allow a secure diagnosis to be made, necessitating biopsy and dermatopathological assessment. Coupled with robust clinical assessment, biopsy findings can guide genetic testing as, increasingly, the causative genes are known for these conditions. Here we review illustrative examples of appendageal tumours and relevant advances made in genetic discovery, and suggest when referral to a geneticist may need to be considered. © Royal College of Physicians 2017. All rights reserved.

Entities:  

Keywords:  Cancer; FH; FLCN; hair follicle tumours; skin tumour syndromes

Mesh:

Substances:

Year:  2017        PMID: 29196359      PMCID: PMC6297702          DOI: 10.7861/clinmedicine.17-6-562

Source DB:  PubMed          Journal:  Clin Med (Lond)        ISSN: 1470-2118            Impact factor:   2.659


  16 in total

Review 1.  Muir-Torre syndrome.

Authors:  Giovanni Ponti; Maurizio Ponz de Leon
Journal:  Lancet Oncol       Date:  2005-12       Impact factor: 41.316

2.  Multiple cutaneous and uterine leiomyomata resulting from missense mutations in the fumarate hydratase gene.

Authors:  G S Chuang; A Martinez-Mir; D E Engler; R F Gmyrek; A Zlotogorski; A M Christiano
Journal:  Clin Exp Dermatol       Date:  2006-01       Impact factor: 3.470

Review 3.  Genetics of skin appendage neoplasms and related syndromes.

Authors:  D A Lee; M E Grossman; P Schneiderman; J T Celebi
Journal:  J Med Genet       Date:  2005-11       Impact factor: 6.318

Review 4.  Diffuse and segmental variants of cutaneous leiomyomatosis: novel mutations in the fumarate hydratase gene and review of the literature.

Authors:  Sadhanna Badeloe; Michel van Geel; Maurice A M van Steensel; Jesús Bastida; Juan Ferrando; Peter M Steijlen; Jorge Frank; Pamela Poblete-Gutiérrez
Journal:  Exp Dermatol       Date:  2006-09       Impact factor: 3.960

5.  Novel mutations in FH and expansion of the spectrum of phenotypes expressed in families with hereditary leiomyomatosis and renal cell cancer.

Authors:  M-H Wei; O Toure; G M Glenn; M Pithukpakorn; L Neckers; C Stolle; P Choyke; R Grubb; L Middelton; M L Turner; M M Walther; M J Merino; B Zbar; W M Linehan; J R Toro
Journal:  J Med Genet       Date:  2005-06-03       Impact factor: 6.318

6.  Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinoma.

Authors:  Betty Gardie; Audrey Remenieras; Darouna Kattygnarath; Johny Bombled; Sandrine Lefèvre; Victoria Perrier-Trudova; Pierre Rustin; Michel Barrois; Abdelhamid Slama; Marie-Françoise Avril; Didier Bessis; Olivier Caron; Frédéric Caux; Patrick Collignon; Isabelle Coupier; Carol Cremin; Hélène Dollfus; Catherine Dugast; Bernard Escudier; Laurence Faivre; Michel Field; Brigitte Gilbert-Dussardier; Nicolas Janin; Yves Leport; Dominique Leroux; Dan Lipsker; Félicia Malthieu; Barbara McGilliwray; Christine Maugard; Arnaud Méjean; Isabelle Mortemousque; Ghislaine Plessis; Bruce Poppe; Christelle Pruvost-Balland; Serena Rooker; Joelle Roume; Nadem Soufir; Michelle Steinraths; Min-Han Tan; Christine Théodore; Luc Thomas; Pierre Vabres; Emmanuel Van Glabeke; Jean-Baptiste Meric; Virginie Verkarre; Gilbert Lenoir; Virginie Joulin; Sophie Deveaux; Veronica Cusin; Jean Feunteun; Bin Tean Teh; Brigitte Bressac-de Paillerets; Stéphane Richard
Journal:  J Med Genet       Date:  2011-03-12       Impact factor: 6.318

Review 7.  Cutaneous sebaceous neoplasms as markers of Muir-Torre syndrome: a diagnostic algorithm.

Authors:  Ossama Abbas; Meera Mahalingam
Journal:  J Cutan Pathol       Date:  2009-06       Impact factor: 1.587

Review 8.  Cowden syndrome: a critical review of the clinical literature.

Authors:  Robert Pilarski
Journal:  J Genet Couns       Date:  2008-10-30       Impact factor: 2.537

9.  Recurrent pneumothorax.

Authors:  Tom G Hopkins; Eamonn R Maher; Evan Reid; Stefan J Marciniak
Journal:  Lancet       Date:  2011-05-07       Impact factor: 79.321

10.  Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts.

Authors:  Hans F A Vasen; Ignacio Blanco; Katja Aktan-Collan; Jessica P Gopie; Angel Alonso; Stefan Aretz; Inge Bernstein; Lucio Bertario; John Burn; Gabriel Capella; Chrystelle Colas; Christoph Engel; Ian M Frayling; Maurizio Genuardi; Karl Heinimann; Frederik J Hes; Shirley V Hodgson; John A Karagiannis; Fiona Lalloo; Annika Lindblom; Jukka-Pekka Mecklin; Pal Møller; Torben Myrhoj; Fokko M Nagengast; Yann Parc; Maurizio Ponz de Leon; Laura Renkonen-Sinisalo; Julian R Sampson; Astrid Stormorken; Rolf H Sijmons; Sabine Tejpar; Huw J W Thomas; Nils Rahner; Juul T Wijnen; Heikki Juhani Järvinen; Gabriela Möslein
Journal:  Gut       Date:  2013-02-13       Impact factor: 23.059

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  1 in total

Review 1.  Hereditary leiomyomatosis and renal cell carcinoma: a case series and literature review.

Authors:  Zahraa Chayed; Lone Krøldrup Kristensen; Lilian Bomme Ousager; Karina Rønlund; Anette Bygum
Journal:  Orphanet J Rare Dis       Date:  2021-01-18       Impact factor: 4.123

  1 in total

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