Literature DB >> 24898507

[Genodermatoses with malignant skin tumors].

L Hübinger1, J Frank.   

Abstract

Cutaneous malignancies can manifest as isolated and sporadic tumors as well as multiple and disseminated tumors. In the latter case they often point to a genetic disease, which either can be restricted to the skin exclusively or also involve extracutaneous organs in the context of a hereditary tumor syndrome. Such hereditary tumor syndromes are clinically and genetically very heterogeneous. Therefore, the prevailing specific skin tumors play an important diagnostic role in the case of complex symptom constellations. Elucidation of the genetic basis of rare monogenetically inherited disorders and syndromes can contribute to a better understanding of the pathogenesis of frequently occurring cutaneous malignancies because the mutated genes often encode proteins, which have a key position in metabolic signaling pathways that are of high significance for the development of targeted therapies. Here we provide an overview of genodermatoses, which are associated with basal cell carcinomas, sebaceous carcinomas, keratoacanthomas, squamous cell carcinomas and malignant melanomas.

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Year:  2014        PMID: 24898507     DOI: 10.1007/s00105-013-2715-x

Source DB:  PubMed          Journal:  Hautarzt        ISSN: 0017-8470            Impact factor:   0.751


  46 in total

Review 1.  Xeroderma pigmentosum--bridging a gap between clinic and laboratory.

Authors:  S Moriwaki; K H Kraemer
Journal:  Photodermatol Photoimmunol Photomed       Date:  2001-04       Impact factor: 3.135

2.  [Spinocellular epitheliomas in congenital cutaneous atrophy in 2 families with high cancer morbidity].

Authors:  C HURIEZ; P AGACHE; M BOMBART; F SOUILLIART
Journal:  Bull Soc Fr Dermatol Syphiligr       Date:  1963 Jan-Mar

3.  Cancer and neurologic degeneration in xeroderma pigmentosum: long term follow-up characterises the role of DNA repair.

Authors:  Porcia T Bradford; Alisa M Goldstein; Deborah Tamura; Sikandar G Khan; Takahiro Ueda; Jennifer Boyle; Kyu-Seon Oh; Kyoko Imoto; Hiroki Inui; Shin-Ichi Moriwaki; Steffen Emmert; Kristen M Pike; Arati Raziuddin; Teri M Plona; John J DiGiovanna; Margaret A Tucker; Kenneth H Kraemer
Journal:  J Med Genet       Date:  2010-11-19       Impact factor: 6.318

4.  [Congenital hypotrichosis and milia with spontaneous regression during adolescence or Oley syndrome: a variant of Bazex-Dupré-Christol syndrome].

Authors:  V Andreani; M Richard; G Folchetti; S Varennes; N Philip; J J Grob
Journal:  Ann Dermatol Venereol       Date:  2000-03       Impact factor: 0.777

5.  Multiple sebaceous tumors.

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

6.  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

Review 7.  Crosslinks and crosstalk: human cancer syndromes and DNA repair defects.

Authors:  Mary A Risinger; Joanna Groden
Journal:  Cancer Cell       Date:  2004-12       Impact factor: 31.743

8.  Multiple familial and pigmented basal cell carcinomas in early childhood - Bazex-Dupré-Christol syndrome.

Authors:  F Abuzahra; L J M T Parren; J Frank
Journal:  J Eur Acad Dermatol Venereol       Date:  2011-03-24       Impact factor: 6.166

Review 9.  A systematic review of worldwide incidence of nonmelanoma skin cancer.

Authors:  A Lomas; J Leonardi-Bee; F Bath-Hextall
Journal:  Br J Dermatol       Date:  2012-05       Impact factor: 9.302

10.  The role of sunlight and DNA repair in melanoma and nonmelanoma skin cancer. The xeroderma pigmentosum paradigm.

Authors:  K H Kraemer; M M Lee; A D Andrews; W C Lambert
Journal:  Arch Dermatol       Date:  1994-08
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