1 Department of Pediatrics, Columbia University College of Physicians and Surgeons, Babies Hospital, Children's Medical and Surgical Center, and the Edward Daniels Faulkner Arthritis Clinic, Columbia-Presbyterian Medical Center, New York, New York
Modern treatment of childhood dermatomyositis with corticosteroids has resulted in greatly improved prognosis and style of life. The immunosuppressive drugs methotrexate and azathioprine have been utilized as ancillary agents in life-threatening disease and in children whose disease could not be adequately controlled with prednisone alone. Two patients are completely well without medication two and seven years after onset; two have received no medications for more than two years and have only subtle signs of any residual illness although they had been profoundly ill for two to three years after the onset of dermatomyositis. A fifth patient, completing the third year of disease, remains ill and continues to require medications but has improved sufficiently to return to regular class in school.
Submitted on March 12, 1976
This article has been cited by other articles:
![]() |
Y.-t. Ng, R. A. Ouvrier, and T. Wu Drug Therapy in Juvenile Dermatomyositis: Follow-Up Study J Child Neurol, March 1, 1998; 13(3): 109 - 112. [Abstract] [PDF] |
||||
![]() |
H. M. Schroter, H. B. Sarnat, D. S. Matheson, and T. P. Seland Juvenile Dermatomyositis Induced by Toxoplasmosis J Child Neurol, April 1, 1987; 2(2): 101 - 104. [Abstract] [PDF] |
||||