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dc.contributorSistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP-
dc.contributor.authorSZEIMIES, R. M.-
dc.contributor.authorTOREZAN, L.-
dc.contributor.authorNIWA, A.-
dc.contributor.authorVALENTE, N.-
dc.contributor.authorUNGER, P.-
dc.contributor.authorKOHL, E.-
dc.contributor.authorSCHREML, S.-
dc.contributor.authorBABILAS, P.-
dc.contributor.authorKARRER, S.-
dc.contributor.authorFESTA-NETO, C.-
dc.date.accessioned2013-07-30T14:43:47Z-
dc.date.available2013-07-30T14:43:47Z-
dc.date.issued2012-
dc.identifier.citationBRITISH JOURNAL OF DERMATOLOGY, v.167, n.1, p.150-159, 2012-
dc.identifier.issn0007-0963-
dc.identifier.urihttps://observatorio.fm.usp.br/handle/OPI/560-
dc.description.abstractBackground The field cancerization concept in photodamaged patients suggests that the entire sun-exposed surface of the skin has an increased risk for the development of (pre)-malignant lesions, mainly epithelial tumours. Topical photodynamic therapy (PDT) is a noninvasive therapeutic method for multiple actinic keratosis (AK) with excellent outcome. Objectives To evaluate the clinical, histological and immunohistochemical changes in human skin with field cancerization after multiple sessions of PDT with methyl-aminolaevulinate (MAL). Methods Twenty-six patients with photodamaged skin and multiple AK on the face received three consecutive sessions of MAL-PDT with red light (37 J cm(-2)), 1 month apart. Biopsies before and 3 months after the last treatment session were taken from normal-appearing skin on the field-cancerized area. Immunohistochemical stainings were performed for TP-53, procollagen-I, metalloproteinase-1 (MMP-1) and tenascin-C (Tn-C). Results All 26 patients completed the study. The global score for photodamage improved considerably in all patients (P < 0.001). The AK clearance rate was 89.5% at the end of the study. Two treatment sessions were as effective as three MAL-PDT sessions. A significant decrease in atypia grade and extent of keratinocyte atypia was observed histologically (P < 0.001). Also, a significant increase in collagen deposition (P = 0.001) and improvement of solar elastosis (P = 0.002) were noticed after PDT. However, immunohistochemistry showed only a trend for decreased TP-53 expression (not significant), increased procollagen-I and MMP-1 expressions (not significant) and an increased expression of Tn-C (P = 0.024). Conclusions Clinical and histological improvement in field cancerization after multiple sessions of MAL-PDT is proven. The decrease in severity and extent of keratinocyte atypia associated with a decreased expression of TP-53 suggest a reduced carcinogenic potential of the sun-damaged area. The significant increase of new collagen deposition and the reduction of solar elastosis explain the clinical improvement of photodamaged skin.-
dc.description.sponsorshipAlmirall-
dc.description.sponsorshipBiofrontera-
dc.description.sponsorshipEnergist-
dc.description.sponsorshipGalderma-
dc.description.sponsorshipIntendis-
dc.description.sponsorshipNovartis-
dc.description.sponsorshipPhotonamic-
dc.description.sponsorshipWyeth-
dc.language.isoeng-
dc.publisherWILEY-BLACKWELL-
dc.relation.ispartofBritish Journal of Dermatology-
dc.rightsrestrictedAccess-
dc.subject.otherhuman epidermal-keratinocytes-
dc.subject.othersquamous-cell carcinoma-
dc.subject.otherintense pulsed-light-
dc.subject.other5-aminolevulinic acid-
dc.subject.otheractinic keratoses-
dc.subject.othermethyl-aminolevulinate-
dc.subject.othertenascin-c-
dc.subject.othermatrix metalloproteinases-
dc.subject.othertransplant recipients-
dc.subject.othertopical application-
dc.titleClinical, histopathological and immunohistochemical assessment of human skin field cancerization before and after photodynamic therapy-
dc.typearticle-
dc.rights.holderCopyright WILEY-BLACKWELL-
dc.identifier.doi10.1111/j.1365-2133.2012.10887.x-
dc.identifier.pmid22329784-
dc.subject.wosDermatology-
dc.type.categoryoriginal article-
dc.type.versionpublishedVersion-
hcfmusp.author.externalSZEIMIES, R. M.:Regensburg Univ Hosp, Dept Dermatol, Regensburg, Germany-
hcfmusp.author.externalNIWA, A.:Univ Sao Paulo, Hosp Clin, Dept Dermatol, Sao Paulo, Brazil-
hcfmusp.author.externalUNGER, P.:Regensburg Univ Hosp, Dept Dermatol, Regensburg, Germany-
hcfmusp.author.externalKOHL, E.:Regensburg Univ Hosp, Dept Dermatol, Regensburg, Germany-
hcfmusp.author.externalSCHREML, S.:Regensburg Univ Hosp, Dept Dermatol, Regensburg, Germany-
hcfmusp.author.externalBABILAS, P.:Regensburg Univ Hosp, Dept Dermatol, Regensburg, Germany-
hcfmusp.author.externalKARRER, S.:Regensburg Univ Hosp, Dept Dermatol, Regensburg, Germany-
hcfmusp.description.beginpage150-
hcfmusp.description.endpage159-
hcfmusp.description.issue1-
hcfmusp.description.volume167-
hcfmusp.origemWOS-
hcfmusp.origem.id2-s2.0-84863334715-
hcfmusp.origem.idWOS:000305791500024-
hcfmusp.publisher.cityHOBOKEN-
hcfmusp.publisher.countryUSA-
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dc.description.indexMEDLINE-
hcfmusp.remissive.sponsorshipNovartis-
hcfmusp.remissive.sponsorshipPfizer-
hcfmusp.remissive.sponsorshipNovartis-
hcfmusp.remissive.sponsorshipPfizer-
hcfmusp.lim.ref2012-
hcfmusp.citation.scopus100-
hcfmusp.scopus.lastupdate2022-07-29-
Appears in Collections:

Artigos e Materiais de Revistas Científicas - FM/MDT
Departamento de Dermatologia - FM/MDT

Artigos e Materiais de Revistas Científicas - HC/ICHC
Instituto Central - HC/ICHC

Artigos e Materiais de Revistas Científicas - LIM/53
LIM/53 - Laboratório de Micologia


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