A dermatopathic Juvenile Dermatomyositis; An Unexpected Case in Childhood

被引：1

作者：

Hassas Yeganeh, Mehrnoush ^{[1
]}

Ahmadi, Pooria ^{[2
]}

Nilipour, Yalda ^{[3
]}

Musavi Khorshidi, Mohaddeseh Sadat ^{[4
]}

Sinaei, Reza ^{[5
]}

Fathi, Mohammad Reza ^{[6
]}

Shiari, Reza ^{[1
]}

机构：

[1] Shahid Beheshti Univ Med Sci, Dept Pediat, Div Pediat Rheumatol, Tehran, Iran

[2] Shahid Beheshti Univ Med Sci, Med Sch, Tehran, Iran

[3] Shahid Beheshti Univ Med Sci, Pediat Pathol Res Ctr, Res Inst Children S Hlth, Tehran, Iran

[4] Shahid Beheshti Univ Med Sci, Dept Pediat, Tehran, Iran

[5] Kerman Univ Med Sci, Pediat Rheumatol, Kerman, Iran

[6] Ahwaz Jundishapur Univ Med Sci, Pediat Rheumatol, Ahvaz, Iran

来源：

IRANIAN JOURNAL OF CHILD NEUROLOGY | 2020年 / 14卷 / 03期

关键词：

Dermatopathic; Juvenile Dermatomyositis; Treatment; POLYMYOSITIS; RITUXIMAB;

D O I：

10.22037/ijcn.v14i3.21686

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

Juvenile dermatomyositis (JDM) is a rare idiopathic inflammatory disease, which usually presents with skin rashes along with muscle weakness. We report a case of JDM in a 10-year-old girl with no skin manifestations presenting with progressive muscle weakness and fatigue. Further laboratory investigations, along with a muscle biopsy, confirmed the diagnosis of adermatopathic JDM. The patient was treated with intravenous immunoglobulin, corticosteroids, methotrexate, hydroxychloroquine, pamidronate, and rituximab. Following treatment, patients' symptoms subsided, and she gained normal muscular strength over a year.

引用

页码：89 / 92

页数：4

共 7 条

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