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Magnetic Resonance Imaging Evaluation in Patients with Linear Morphea Treated with Methotrexate and High-Dose Corticosteroid

BACKGROUND: Morphea is an inflammatory disease of the connective tissue that may lead to thickening and hardening of the skin due to fibrosis. The aim of this study was to document magnetic resonance imaging (MRI) changes in patients with linear morphea who were treated with methotrexate (MTX) and h...

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Autores principales: Shahidi-Dadras, Mohammad, Abdollahimajd, Fahimeh, Jahangard, Razieh, Javinani, Ali, Ashraf-Ganjouei, Amir, Toossi, Parviz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6051098/
https://www.ncbi.nlm.nih.gov/pubmed/30057597
http://dx.doi.org/10.1155/2018/8391218
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author Shahidi-Dadras, Mohammad
Abdollahimajd, Fahimeh
Jahangard, Razieh
Javinani, Ali
Ashraf-Ganjouei, Amir
Toossi, Parviz
author_facet Shahidi-Dadras, Mohammad
Abdollahimajd, Fahimeh
Jahangard, Razieh
Javinani, Ali
Ashraf-Ganjouei, Amir
Toossi, Parviz
author_sort Shahidi-Dadras, Mohammad
collection PubMed
description BACKGROUND: Morphea is an inflammatory disease of the connective tissue that may lead to thickening and hardening of the skin due to fibrosis. The aim of this study was to document magnetic resonance imaging (MRI) changes in patients with linear morphea who were treated with methotrexate (MTX) and high-dose corticosteroid. METHODS: This study was conducted on 33 patients from the outpatient's dermatology clinic of our institute, who fulfilled the inclusion criteria. Patients received 15 mg/week of MTX and monthly pulses of methylprednisolone for three days in six months. The effectiveness of the treatment was evaluated by MRI, modified LS skin severity index (mLoSSI), and localized scleroderma damage index (LoSDI). RESULTS: All parameters of mLoSSI and LoSDI including erythema, skin thickness, new lesion/lesion extension, dermal atrophy, subcutaneous atrophy, and dyspigmentation were also noticeably improved after treatment. Subcutaneous fat enhancement was the most common finding in MRI. MRI scores were significantly associated with clinical markers both before and after the treatment with the exception of skin thickness and new lesion/lesion extension which were not associated with MRI scores before and after the treatment, respectively. LIMITATIONS: The lack of correlative laboratory disease activity markers, control group, and clearly defined criteria to judge the MRI changes. CONCLUSION: MRI could be a promising tool for the assessment of musculoskeletal and dermal involvement and also monitoring treatment response in patients with morphea.
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spelling pubmed-60510982018-07-29 Magnetic Resonance Imaging Evaluation in Patients with Linear Morphea Treated with Methotrexate and High-Dose Corticosteroid Shahidi-Dadras, Mohammad Abdollahimajd, Fahimeh Jahangard, Razieh Javinani, Ali Ashraf-Ganjouei, Amir Toossi, Parviz Dermatol Res Pract Clinical Study BACKGROUND: Morphea is an inflammatory disease of the connective tissue that may lead to thickening and hardening of the skin due to fibrosis. The aim of this study was to document magnetic resonance imaging (MRI) changes in patients with linear morphea who were treated with methotrexate (MTX) and high-dose corticosteroid. METHODS: This study was conducted on 33 patients from the outpatient's dermatology clinic of our institute, who fulfilled the inclusion criteria. Patients received 15 mg/week of MTX and monthly pulses of methylprednisolone for three days in six months. The effectiveness of the treatment was evaluated by MRI, modified LS skin severity index (mLoSSI), and localized scleroderma damage index (LoSDI). RESULTS: All parameters of mLoSSI and LoSDI including erythema, skin thickness, new lesion/lesion extension, dermal atrophy, subcutaneous atrophy, and dyspigmentation were also noticeably improved after treatment. Subcutaneous fat enhancement was the most common finding in MRI. MRI scores were significantly associated with clinical markers both before and after the treatment with the exception of skin thickness and new lesion/lesion extension which were not associated with MRI scores before and after the treatment, respectively. LIMITATIONS: The lack of correlative laboratory disease activity markers, control group, and clearly defined criteria to judge the MRI changes. CONCLUSION: MRI could be a promising tool for the assessment of musculoskeletal and dermal involvement and also monitoring treatment response in patients with morphea. Hindawi 2018-07-02 /pmc/articles/PMC6051098/ /pubmed/30057597 http://dx.doi.org/10.1155/2018/8391218 Text en Copyright © 2018 Mohammad Shahidi-Dadras et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Study
Shahidi-Dadras, Mohammad
Abdollahimajd, Fahimeh
Jahangard, Razieh
Javinani, Ali
Ashraf-Ganjouei, Amir
Toossi, Parviz
Magnetic Resonance Imaging Evaluation in Patients with Linear Morphea Treated with Methotrexate and High-Dose Corticosteroid
title Magnetic Resonance Imaging Evaluation in Patients with Linear Morphea Treated with Methotrexate and High-Dose Corticosteroid
title_full Magnetic Resonance Imaging Evaluation in Patients with Linear Morphea Treated with Methotrexate and High-Dose Corticosteroid
title_fullStr Magnetic Resonance Imaging Evaluation in Patients with Linear Morphea Treated with Methotrexate and High-Dose Corticosteroid
title_full_unstemmed Magnetic Resonance Imaging Evaluation in Patients with Linear Morphea Treated with Methotrexate and High-Dose Corticosteroid
title_short Magnetic Resonance Imaging Evaluation in Patients with Linear Morphea Treated with Methotrexate and High-Dose Corticosteroid
title_sort magnetic resonance imaging evaluation in patients with linear morphea treated with methotrexate and high-dose corticosteroid
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6051098/
https://www.ncbi.nlm.nih.gov/pubmed/30057597
http://dx.doi.org/10.1155/2018/8391218
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