Juvenile dermatomyositis: clinical, laboratorial, histological, therapeutical and evolutive parameters of 35 patients

This study was based on a prospective and a retrospective analysis of 35 patients who met Bohan and Peter criteria for juvenile dermatomyositis diagnosis.The mean follow-up time was three years ten months. Calcinosis was present in five (14.28 %) patients, cutaneous ulcers in four (11.42%), and syst...

Full description

Saved in:
Bibliographic Details
Main Authors: Adriana Maluf Elias Sallum, Maria Helena Bittencurt Kiss, Silvana Sachetti, Maria Bernadate Dutra Resende, Kelly Cristina Moutinho, Mary de Souza Carvalho, Clovis Arthur Almeida Silva, Suely Kazue Nagahashi Marie
Format: Article
Language:English
Published: Thieme Revinter Publicações 2002-12-01
Series:Arquivos de Neuro-Psiquiatria
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2002000600001&tlng=en
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1849744381459824640
author Adriana Maluf Elias Sallum
Maria Helena Bittencurt Kiss
Silvana Sachetti
Maria Bernadate Dutra Resende
Kelly Cristina Moutinho
Mary de Souza Carvalho
Clovis Arthur Almeida Silva
Suely Kazue Nagahashi Marie
author_facet Adriana Maluf Elias Sallum
Maria Helena Bittencurt Kiss
Silvana Sachetti
Maria Bernadate Dutra Resende
Kelly Cristina Moutinho
Mary de Souza Carvalho
Clovis Arthur Almeida Silva
Suely Kazue Nagahashi Marie
author_sort Adriana Maluf Elias Sallum
collection DOAJ
description This study was based on a prospective and a retrospective analysis of 35 patients who met Bohan and Peter criteria for juvenile dermatomyositis diagnosis.The mean follow-up time was three years ten months. Calcinosis was present in five (14.28 %) patients, cutaneous ulcers in four (11.42%), and systemic involvement in nine (27.71%) patients. All patients presented alterations in the serum levels of muscle enzymes, and all of them were submitted to muscle biopsy as a diagnostic procedure. Nine (25.71%) patients received corticotherapy prior to and 26 (74.28%) after the muscle biopsy. Chloroquine, methotrexate, cyclosporine, cyclophosphamide and intravenous immunoglobulin were used in patients with poor response to corticotherapy. Continuation of cutaneous manifestations was observed in 4 (11.43%) patients, laboratorial activity in 1 (2.85%), cutaneous and laboratorial activities in 3 (8.57%). Ten (28.57%) patients were out of activity, and 17 (48.57%) in remission at study end-point, on March 2002. Two (5.71%) patients died.
format Article
id doaj-art-a2d388f1923b4dbcbe9998e4c11b3b0c
institution DOAJ
issn 1678-4227
language English
publishDate 2002-12-01
publisher Thieme Revinter Publicações
record_format Article
series Arquivos de Neuro-Psiquiatria
spelling doaj-art-a2d388f1923b4dbcbe9998e4c11b3b0c2025-08-20T03:19:57ZengThieme Revinter PublicaçõesArquivos de Neuro-Psiquiatria1678-42272002-12-0160488989910.1590/S0004-282X2002000600001Juvenile dermatomyositis: clinical, laboratorial, histological, therapeutical and evolutive parameters of 35 patientsAdriana Maluf Elias Sallum0Maria Helena Bittencurt Kiss1Silvana Sachetti2Maria Bernadate Dutra Resende3Kelly Cristina Moutinho4Mary de Souza Carvalho5Clovis Arthur Almeida Silva6Suely Kazue Nagahashi Marie7Universidade de São PauloUniversidade de São PauloSão Paulo Medical SchoolUniversidade de São PauloUniversidade de São PauloUniversidade de São PauloUniversidade de São PauloUniversidade de São PauloThis study was based on a prospective and a retrospective analysis of 35 patients who met Bohan and Peter criteria for juvenile dermatomyositis diagnosis.The mean follow-up time was three years ten months. Calcinosis was present in five (14.28 %) patients, cutaneous ulcers in four (11.42%), and systemic involvement in nine (27.71%) patients. All patients presented alterations in the serum levels of muscle enzymes, and all of them were submitted to muscle biopsy as a diagnostic procedure. Nine (25.71%) patients received corticotherapy prior to and 26 (74.28%) after the muscle biopsy. Chloroquine, methotrexate, cyclosporine, cyclophosphamide and intravenous immunoglobulin were used in patients with poor response to corticotherapy. Continuation of cutaneous manifestations was observed in 4 (11.43%) patients, laboratorial activity in 1 (2.85%), cutaneous and laboratorial activities in 3 (8.57%). Ten (28.57%) patients were out of activity, and 17 (48.57%) in remission at study end-point, on March 2002. Two (5.71%) patients died.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2002000600001&tlng=enjuvenile dermatomyositisclinical findingsmuscle biopsytreatmentevolutionoutcome
spellingShingle Adriana Maluf Elias Sallum
Maria Helena Bittencurt Kiss
Silvana Sachetti
Maria Bernadate Dutra Resende
Kelly Cristina Moutinho
Mary de Souza Carvalho
Clovis Arthur Almeida Silva
Suely Kazue Nagahashi Marie
Juvenile dermatomyositis: clinical, laboratorial, histological, therapeutical and evolutive parameters of 35 patients
Arquivos de Neuro-Psiquiatria
juvenile dermatomyositis
clinical findings
muscle biopsy
treatment
evolution
outcome
title Juvenile dermatomyositis: clinical, laboratorial, histological, therapeutical and evolutive parameters of 35 patients
title_full Juvenile dermatomyositis: clinical, laboratorial, histological, therapeutical and evolutive parameters of 35 patients
title_fullStr Juvenile dermatomyositis: clinical, laboratorial, histological, therapeutical and evolutive parameters of 35 patients
title_full_unstemmed Juvenile dermatomyositis: clinical, laboratorial, histological, therapeutical and evolutive parameters of 35 patients
title_short Juvenile dermatomyositis: clinical, laboratorial, histological, therapeutical and evolutive parameters of 35 patients
title_sort juvenile dermatomyositis clinical laboratorial histological therapeutical and evolutive parameters of 35 patients
topic juvenile dermatomyositis
clinical findings
muscle biopsy
treatment
evolution
outcome
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2002000600001&tlng=en
work_keys_str_mv AT adrianamalufeliassallum juveniledermatomyositisclinicallaboratorialhistologicaltherapeuticalandevolutiveparametersof35patients
AT mariahelenabittencurtkiss juveniledermatomyositisclinicallaboratorialhistologicaltherapeuticalandevolutiveparametersof35patients
AT silvanasachetti juveniledermatomyositisclinicallaboratorialhistologicaltherapeuticalandevolutiveparametersof35patients
AT mariabernadatedutraresende juveniledermatomyositisclinicallaboratorialhistologicaltherapeuticalandevolutiveparametersof35patients
AT kellycristinamoutinho juveniledermatomyositisclinicallaboratorialhistologicaltherapeuticalandevolutiveparametersof35patients
AT marydesouzacarvalho juveniledermatomyositisclinicallaboratorialhistologicaltherapeuticalandevolutiveparametersof35patients
AT clovisarthuralmeidasilva juveniledermatomyositisclinicallaboratorialhistologicaltherapeuticalandevolutiveparametersof35patients
AT suelykazuenagahashimarie juveniledermatomyositisclinicallaboratorialhistologicaltherapeuticalandevolutiveparametersof35patients