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Rapid improvement of calcinosis in juvenile dermatomyositis with alendronate therapy.

Abstract
A 6-year-old boy with improving juvenile dermatomyositis (JDM) developed severe and debilitating calcinosis, unresponsive to diltiazem and probenecid. Alendronate produced dramatic improvement within 1 month and by 12 months calcinosis had virtually resolved. The response was followed by bone mineral content measurements.
AuthorsGeoffrey R Ambler, Jeffrey Chaitow, Maureen Rogers, David W McDonald, Robert A Ouvrier
JournalThe Journal of rheumatology (J Rheumatol) Vol. 32 Issue 9 Pg. 1837-9 (Sep 2005) ISSN: 0315-162X [Print] Canada
PMID16142885 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Prednisone
  • Alendronate
  • Methotrexate
Topics
  • Alendronate (administration & dosage)
  • Calcinosis (diagnostic imaging, drug therapy, etiology)
  • Child
  • Dermatomyositis (complications, diagnostic imaging, drug therapy)
  • Dose-Response Relationship, Drug
  • Drug Administration Schedule
  • Drug Therapy, Combination
  • Follow-Up Studies
  • Humans
  • Male
  • Methotrexate (administration & dosage)
  • Prednisone (administration & dosage)
  • Radiography
  • Risk Assessment
  • Severity of Illness Index
  • Treatment Outcome

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