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Calcinosis in juvenile dermatomyositis: frequency, risk factors and outcome

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Abstract

The aim was to retrospectively estimate the prevalence of calcinosis in patients with juvenile dermatomyositis (JDM) and to identify risk factors associated with development of calcinosis in these patients. Retrospective chart review of 39 children diagnosed with JDM between 2004 and 2015 in a tertiary care hospital was done. Patients were divided into two groups, depending on the presence or absence of calcinosis, and the two groups were compared with respect to demographic, clinical, laboratory and therapeutic characteristics. Calcinosis developed in nine (23.1 %) patients. Delay in diagnosis and initiation of treatment, prolonged duration of disease, the presence of joint contractures and cardiac involvement were significantly associated with increased frequency of calcinosis. Six out of nine (66.7 %) patients with calcinosis received alendronate therapy, out of which four showed partial reduction in calcinosis. In one case, surgical removal of tumorous clumps was done. Calcinosis remains a common complication of JDM. We found an association between calcinosis and delay in diagnosis and initiation of treatment, prolonged duration of disease and cardiac involvement. Our study suggests that alendronate may be beneficial in management of calcinosis of JDM.

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Author contributions

IS contributed to data collection, analysis and manuscript writing; SKK contributed to data collection, analysis, manuscript writing and was a guarantor for the study; and MK analyzed data and wrote manuscript.

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Correspondence to Sushil Kumar Kabra.

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Author Isha Saini declares that she has no conflict of interest. Author Mani Kalaivani declares that she has no conflict of interest, and author Sushil Kumar Kabra declares that he has no conflict of interest.

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Not required as it was retrospective chart review and none of the patients enrolled in study have been identified by name.

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Saini, I., Kalaivani, M. & Kabra, S.K. Calcinosis in juvenile dermatomyositis: frequency, risk factors and outcome. Rheumatol Int 36, 961–965 (2016). https://doi.org/10.1007/s00296-016-3467-6

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  • DOI: https://doi.org/10.1007/s00296-016-3467-6

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