Localized scleroderma and related comorbidities: a single centre cohort study

dc.contributor.authorKortelainen, Saara
dc.contributor.authorHieta, Niina
dc.contributor.authorRissanen, Tiia
dc.contributor.authorPaltta, Johanna
dc.contributor.authorPirilä, Laura
dc.contributor.authorKähäri, Veli-Matti
dc.contributor.organizationfi=biostatistiikka|en=Biostatistics|
dc.contributor.organizationfi=iho- ja sukupuolitautioppi|en=Dermatology and Venereology|
dc.contributor.organizationfi=sisätautioppi|en=Internal Medicine|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code1.2.246.10.2458963.20.39855016430
dc.contributor.organization-code1.2.246.10.2458963.20.40502528769
dc.contributor.organization-code1.2.246.10.2458963.20.89365200099
dc.converis.publication-id505045950
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/505045950
dc.date.accessioned2026-01-21T12:20:23Z
dc.date.available2026-01-21T12:20:23Z
dc.description.abstract<p>Background: Localized scleroderma, or morphea is a rare autoimmune disease that affects the skin and underlying tissue. It is more common in females than males. The incidence has two peaks, one in childhood and another in middle-age. Concomitant autoimmune diseases are frequently observed, whereas systemic sclerosis occurs rarely simultaneously.</p><p>Objectives: This study aimed to assess the clinical features, comorbidities, and treatments of localized scleroderma in Southwest Finland.</p><p>Methods: Patients diagnosed with localized scleroderma (ICD-10 code L94) treated between January 1, 2005 and November 30, 2020, were identified from the hospital discharge register of Turku University Hospital. Diagnoses were classified into five main types and their subtypes based on the European Dermatology Forum (EDF) criteria. Basic demographic data, associated comorbidities, treatments used, and their efficacy were collected.</p><p>Results: A total of 155 patients with morphea were included, with 125 females (80.6%) and 30 males (19.4%). The most common subtype was limited, plaque-type morphea (n=71, 45.8% of all patients), followed by the generalized type (n=57, 36.8%). Fifty-nine concomitant autoimmune diseases were identified in 45 patients (29.0%), most frequently autoimmune thyroid diseases (n=23, 14.8%). Simultaneous systemic sclerosis was rare (n=3, 1.9%). The most common malignancy was breast cancer (n=11, 7.1%). Extracutaneous manifestations were more common in pediatric-onset patients (18.5%) than in adult-onset patients (1.7%). The most commonly used systemic treatment was methotrexate (n=25, 16.1%) which was beneficial for 64% of treated patients. Phototherapy was administered to 63 patients (40.6%) and it was beneficial for 49 patients (77.8%).</p><p>Conclusions: Patients with morphea at our centre often required systemic immunomodulatory treatment or phototherapy. The incidence of the generalized subtype and the occurrence of concomitant autoimmune diseases, particularly thyroid autoimmune diseases, were relatively high. No evidence of an increased risk of malignancy was observed among these patients.</p>
dc.identifier.eissn1365-2133
dc.identifier.jour-issn0007-0963
dc.identifier.olddbid212359
dc.identifier.oldhandle10024/195377
dc.identifier.urihttps://www.utupub.fi/handle/11111/51592
dc.identifier.urlhttps://doi.org/10.1093/bjd/ljaf419
dc.identifier.urnURN:NBN:fi-fe202601215787
dc.language.isoen
dc.okm.affiliatedauthorKortelainen, Saara
dc.okm.affiliatedauthorHieta, Niina
dc.okm.affiliatedauthorRissanen, Tiia
dc.okm.affiliatedauthorPaltta, Johanna
dc.okm.affiliatedauthorPirilä, Laura
dc.okm.affiliatedauthorKähäri, Veli-Matti
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3121 Internal medicineen_GB
dc.okm.discipline3121 Sisätauditfi_FI
dc.okm.internationalcopublicationnot an international co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherOxford University Press (OUP)
dc.publisher.countryUnited Kingdomen_GB
dc.publisher.countryBritanniafi_FI
dc.publisher.country-codeGB
dc.relation.articlenumberljaf419
dc.relation.doi10.1093/bjd/ljaf419
dc.relation.ispartofjournalBritish Journal of Dermatology
dc.source.identifierhttps://www.utupub.fi/handle/10024/195377
dc.titleLocalized scleroderma and related comorbidities: a single centre cohort study
dc.year.issued2025

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