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               <dc:title>Actinic Keratosis, a Chronic, Progressive Disease: Understanding Clinical Gaps to Optimise Patient Management</dc:title>
               <dc:creator>Cerio, Rino</dc:creator>
               <dc:creator>Dirschka, Thomas</dc:creator>
               <dc:creator>Dréno, Brigitte</dc:creator>
               <dc:creator>Figueras Nart, Ignasi</dc:creator>
               <dc:creator>Lear, John T.</dc:creator>
               <dc:creator>Pellacani, Giovanni</dc:creator>
               <dc:creator>Peris, Ketty</dc:creator>
               <dc:creator>Ruiz de Casas, Andrés</dc:creator>
               <dc:subject>Tumors</dc:subject>
               <dc:subject>Malalties de la pell</dc:subject>
               <dc:subject>Skin diseases</dc:subject>
               <dc:description>Actinic keratosis (AK) is a chronic, progressive disease&#xd;
of the skin that has undergone long-term sun exposure.&#xd;
The affected areas contain visible and subclinical nonvisible&#xd;
sun damage resulting in epidermal keratinocyte&#xd;
dysplasia, known by many as ‘field cancerisation’ (1),&#xd;
which is prone to AKs and sun-related skin cancer (2).&#xd;
Thus, visible AKs are clinical biomarkers for a photo-damaged&#xd;
field with subclinical damage associated with the&#xd;
unpredictable risk of progression to invasive squamous&#xd;
cell carcinoma (iSCC) (3). The aim of this multiexpert&#xd;
opinion article is to provide a discussion succinctly&#xd;
highlighting the clinical gaps for optimal management of&#xd;
AK: the lack of a universal definition and the need for a&#xd;
standardised grade assessment of AK/field cancerisation&#xd;
that also takes into account individual risk.</dc:description>
               <dc:date>2018-09-05T07:57:46Z</dc:date>
               <dc:date>2018-09-05T07:57:46Z</dc:date>
               <dc:date>2017-09-01</dc:date>
               <dc:date>2018-07-24T12:01:41Z</dc:date>
               <dc:type>info:eu-repo/semantics/article</dc:type>
               <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
               <dc:relation>Reproducció del document publicat a: https://doi.org/10.2340/00015555-2692</dc:relation>
               <dc:relation>Acta Dermato-Venereologica, 2017, vol. 97, num. 8, p. 997-998</dc:relation>
               <dc:relation>https://doi.org/10.2340/00015555-2692</dc:relation>
               <dc:rights>cc by-nc (c) Acta Dermato-Venereologica, 2017</dc:rights>
               <dc:rights>http://creativecommons.org/licenses/by-nc/3.0/es/</dc:rights>
               <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
               <dc:publisher>Acta Dermato-Venereologica</dc:publisher>
               <dc:source>Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))</dc:source>
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