A fatal presentation of dermatomyositis with facial swelling

被引:4
|
作者
Dwivedi, Nishant [1 ]
Michael, Christie [2 ]
Lew, D. Betty [2 ]
Arnold, Sandra [2 ]
Igarashi, Masanori [2 ]
Bertorini, Tulio [3 ]
Thompson, Jerome W. [4 ]
Myers, Linda K. [2 ]
Brown, Monica L. [2 ]
机构
[1] Univ Tennessee, Ctr Hlth Sci, Dept Microbiol Immunol & Biochem, Memphis, TN 38163 USA
[2] Univ Tennessee, Ctr Hlth Sci, Dept Pediat, Memphis, TN 38163 USA
[3] Univ Tennessee, Ctr Hlth Sci, Dept Med, Memphis, TN 38163 USA
[4] Univ Tennessee, Ctr Hlth Sci, Dept Otolaryngol, Memphis, TN 38163 USA
关键词
Periorbital; Edema; Sinusitis; Dermatomyositis; Juvenile; Vasculitis; JUVENILE DERMATOMYOSITIS; PERIORBITAL EDEMA; POLYMYOSITIS; REGISTRY;
D O I
10.1016/j.ijporl.2012.01.037
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Juvenile dermatomyositis (JDM) is the most common inflammatory autoimmune myopathy in children. Most common presentations consist of heliotrophic rash and/or gottron's papules in addition to proximal muscle weakness. A typical presentations have been reported. We present a 13-year-old African American male who presented with a two-week history of bilateral periorbital edema that was unresponsive to glucocorticoids. He had elevated transaminases but no detectable muscle weakness. A muscle biopsy was consistent with juvenile dermatomyositis. This case highlights the need to consider dermatomyositis in cases of facial swelling and the use of aggressive immunosuppressive therapies due to its associated vasculopathies. Published by Elsevier Ireland Ltd.
引用
收藏
页码:745 / 749
页数:5
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