Unrecognized juvenile dermatomyositis complicated by calcinosis universalis: a case report from Cameroon

被引:1
作者
Mandengue, C. E. [1 ]
Nouedoui, C. [1 ]
Atangana, P. J. A. [2 ]
机构
[1] Hop Gen Yaounde, Med Interne, BP 13650, Yaounde, Cameroon
[2] Inst Pasteur Cameroun, Lab Anat Pathol, Yaounde, Cameroon
来源
MEDECINE ET SANTE TROPICALES | 2013年 / 23卷 / 04期
关键词
juvenile dermatomyositis; Cameroon;
D O I
10.1684/mst.2013.0248
中图分类号
R188.11 [热带医学];
学科分类号
摘要
Juvenile dermatomyositis is a rare auto-immune disease that causes inflammation of the skin and muscles. Calcinosis may complicate its course, especially when the diagnosis is late or the corticosteroid therapy inadequate. In those cases, significant joint disability may occur. Few cases are reported in sub-Saharan Africa, probably because it is rarely recognized in these areas. We report the first Cameroonian case, occurring in a 9-year-old girl. Although she sought treatment early in the disease course, the dermatomyositis was diagnosed quite late, after the onset of calcinosis universalis and severe disability. Early diagnosis of the disease and effective treatment are essential to prevent calcinosis universalis from complicating this disease in children.
引用
收藏
页码:458 / 461
页数:4
相关论文
共 11 条
[1]  
Eddy M.C., Leelawattana R., McAlister W.H., Whyte M.P., Calcinosis universalis complicating juvenile dermatomyositis: Resolution during probenecid therapy, J Clin Endocrinol Metab, 82, pp. 3536-3542, (1997)
[2]  
Yun S.J., Lee J.B., Kim S.J., Lee S.C., Won Y.H., Kang H.C., Calcinosis cutis universalis with joint contractures complicating juvenile dermatomyositis, Dermatology, 212, pp. 401-403, (2006)
[3]  
Prieur A.M., Les dermatomyosites de l'enfant, Med Ther Pedia, 3, pp. 102-107, (2000)
[4]  
Jager C., Sirvent N., Rabasse N., Et al., Dermatomyosite juvénile dans la région niçoise. Etude rétrospective 1991-2001, Ann Dermatol Venereol, 129, pp. 1120-1124, (2002)
[5]  
Haudouin V., Les dermatomyosites juvéniles, Med Ther Pedia, 9, pp. 23-27, (2006)
[6]  
Roujeau J.C., Dermatomyosite, (2013)
[7]  
Bughin V., Megharfi W., Prieur A.M., Les outils validés pour le suivi des dermatomyosites juvéniles, Med Ther Pedia, 9, pp. 28-39, (2006)
[8]  
Martin N., Li C.K., Weddenburn L.R., Juvenile dermatomyositis: New insights and new treatment strategies, Ther Adv Musculoskelet Dis, 4, pp. 41-50, (2012)
[9]  
Ravelli A., Trail L., Ferrari C., Et al., Long-term outcome and prognosis factors of juvenile dermatomyositis. A multinational, multicenter study of 490 patients, Arthritis Care Res, 62, pp. 63-72, (2010)
[10]  
Tugnet N., Rees D.H.E., Calcinosis in dermatomyositis, Postgrad Med J, 86, (2010)