2006
DOI: 10.2223/jped.1435
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Inflammatory myopathies in childhood: correlation between nailfold capillaroscopy findings and clinical and laboratory data

Abstract: Nailfold capillaroscopy is a non-invasive examination that offers satisfactory correlation with disease activity and could be a useful tool for the diagnosis and follow-up of inflammatory myopathies.

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Cited by 32 publications
(13 citation statements)
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“…Several studies have reported that the intensity of the morphological changes on NFC correlate with the clinical course and the more severe forms of disease, such as ulcerative complications and calcinosis. [27][28][29][30] In our study, disease activity was associated with capillaroscopic changes, indicating that NFC is an adequate method to monitor the course of JDM.…”
Section: Discussionmentioning
confidence: 85%
“…Several studies have reported that the intensity of the morphological changes on NFC correlate with the clinical course and the more severe forms of disease, such as ulcerative complications and calcinosis. [27][28][29][30] In our study, disease activity was associated with capillaroscopic changes, indicating that NFC is an adequate method to monitor the course of JDM.…”
Section: Discussionmentioning
confidence: 85%
“…NC abnormalities are associated with skin involvement in untreated patients with DM 3 and seem also to correlate with disease activity in inflammatory myopathies 1,2 . DM-specific NC changes in a scleroderma-like pattern 8 provide useful information that contributes to an early diagnosis and helps identify those cases with a poor prognosis 4 .…”
Section: Rheumatologymentioning
confidence: 99%
“…Severe nailfold capillaroscopy (NC) findings have been described but their association with disease activity and/or response to treatment have rarely been investigated [1][2][3][4][5][6][7] .…”
mentioning
confidence: 99%
“…In studies with juvenile DM, the SD pattern is most common, having a positive association with severity and clinical and laboratory activity of the disease. [39][40][41] Mixed connective tissue disease RP is one of the initial manifestations of the disease, occurring in approximately 85% of patients with MCTD and is also part of the main classification criteria for this disease. 42 SD pattern is observed in 50-65% of cases.…”
Section: Dermatomyositis and Polimyositismentioning
confidence: 99%