心膜心筋炎の合併が疑われた抗signal recognition particle(SRP)抗体陽性ミオパチーの1例

Mariko Tanaka, Naoki Gamou, Hirohiko Shizukawa, Emiko Tsuda, Shun Shimohama
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引用次数: 1

Abstract

A 79 year-old female was admitted to our hospital because of high serum creatine kinase level together with proximal muscle weakness and pain on grasping. MRI revealed inflammatory changes in femoral muscles on both sides. Muscle biopsy showed size irregularity of muscle cells, and necrosis and regeneration of fibers. Study of antibodies was also consistent with the diagnostic criteria of anti-signal recognition particle (anti-SRP) antibody-positive myopathy. On admission, the patient required pericardiocentesis for the management of exudative pericarditis. Accompanying the aggravation of myositis, negative T wave in precordial leads on ECG, ventricular extrasystoles and non-sustained ventricular tachycardia were observed. These abnormalities were resolved with the improvement of myositis by immunosuppressive treatment. These observations suggest that the myopericarditis was associated with anti-SRP antibody-positive myopathy.
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怀疑合并心膜心肌炎的抗signal recognition particle (SRP)抗体阳性肌凝片1例
一名79岁女性因血清肌酸激酶水平高并近端肌无力及抓握疼痛而入院。MRI显示两侧股肌炎性改变。肌肉活检显示肌肉细胞大小不规则,纤维坏死和再生。抗体研究也符合抗信号识别颗粒(anti-SRP)抗体阳性肌病的诊断标准。入院时,患者需要心包穿刺治疗渗出性心包炎。伴肌炎加重,心电图心前导联呈负T波,室性心动过速及非持续性室性心动过速。通过免疫抑制治疗,这些异常随着肌炎的改善而消失。这些观察结果提示心包炎与抗srp抗体阳性肌病有关。
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