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dc.contributor.authorRäsänen, J.E.
dc.contributor.authorNeittaanmäki, N.
dc.contributor.authorJeskanen, L.
dc.contributor.authorPölönen, I.
dc.contributor.authorSnellman, E.
dc.contributor.authorGrönroos, M.
dc.date.accessioned2019-09-03T12:06:39Z
dc.date.available2019-09-03T12:06:39Z
dc.date.issued2020
dc.identifier.citationRäsänen, J.E., Neittaanmäki, N., Jeskanen, L., Pölönen, I., Snellman, E., & Grönroos, M. (2020). Ablative fractional laser‐assisted photodynamic therapy for lentigo maligna : a prospective pilot study. <i>Journal of the European Academy of Dermatology and Venereology</i>, <i>34</i>(3), 510-517. <a href="https://doi.org/10.1111/jdv.15925" target="_blank">https://doi.org/10.1111/jdv.15925</a>
dc.identifier.otherCONVID_32689124
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/65412
dc.description.abstractBackground Lentigo maligna (LM) is an in‐situ form of melanoma carrying a risk of progression to invasive lentigo maligna melanoma (LMM). LM poses a clinical challenge, with subclinical extension and high recurrence rates after incomplete surgery. Alternative treatment methods have been investigated with varying results. Photodynamic therapy (PDT) with methylaminolaevulinate (MAL) has already proved promising in this respect. Objectives To investigate the efficacy of ablative fractional laser (AFL)‐assisted PDT with 5‐aminolaevulinic acid nanoemulsion (BF‐200 ALA) for treating LM. Methods In this non‐sponsored, prospective pilot study ten histologically verified LMs were treated with AFL‐assisted PDT three times at two week intervals using a light dose of 90 J/cm2 per treatment session. Local anaesthesia with ropivacain was used. Four weeks after the last PDT treatment the lesions were treated surgically with a wide excision and sent for histopathological examination. The primary outcome was complete histopathological clearance of the LM from the surgical specimen. Patient‐reported pain during illumination and the severity of the skin reaction after the PDT treatments were monitored as secondary outcomes. Results The complete histopathological clearance rate was 7 out of 10 LMs (70%). The pain during illumination was tolerable, with the mean pain scores for the PDT sessions on a visual assessment scale ranging from 2.9 to 3.8. Some severe skin reactions occurred during the treatment period, however. Conclusions AFL‐assisted PDT showed moderate efficacy in terms of histological clearance. It could constitute an alternative treatment for lentigo maligna but due to the side‐effects it should only be considered in inoperable cases.en
dc.format.mimetypeapplication/pdf
dc.languageeng
dc.language.isoeng
dc.publisherWiley-Blackwell Publishing Ltd.
dc.relation.ispartofseriesJournal of the European Academy of Dermatology and Venereology
dc.rightsIn Copyright
dc.subject.otherlentigo maligna
dc.subject.otherphotodynamic therapy
dc.subject.otherablative fractional laser
dc.subject.other5-aminolaevulinic acid nanoemulsion
dc.subject.otherBF-200 ALA
dc.titleAblative fractional laser‐assisted photodynamic therapy for lentigo maligna : a prospective pilot study
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-201909034018
dc.contributor.laitosInformaatioteknologian tiedekuntafi
dc.contributor.laitosFaculty of Information Technologyen
dc.contributor.oppiaineTietotekniikkafi
dc.contributor.oppiaineMathematical Information Technologyen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.format.pagerange510-517
dc.relation.issn0926-9959
dc.relation.numberinseries3
dc.relation.volume34
dc.type.versionacceptedVersion
dc.rights.copyright© European Academy of Dermatology and Venereology, 2019
dc.rights.accesslevelopenAccessfi
dc.subject.ysomelanooma
dc.subject.ysofotodynaaminen hoito
dc.subject.ysolaserhoito
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p15128
jyx.subject.urihttp://www.yso.fi/onto/yso/p2912
jyx.subject.urihttp://www.yso.fi/onto/yso/p18993
dc.rights.urlhttp://rightsstatements.org/page/InC/1.0/?language=en
dc.relation.doi10.1111/jdv.15925
jyx.fundinginformationThis study has been supported by the Cancer Foundation of Finland and by the Tampere University Hospital.
dc.type.okmA1


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