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进行性多发性骨化性肌炎,是一种多发于幼儿,连续或间断的使随意肌、肌膜、腱、腱膜骨膜、韧带等发生进行性骨化,最后全身变成僵硬的一种疾病。国外于1740年Freke首先报导。1858年Muenchmyer报导过18例并做了分析。1898年Stempell曾分析44例文献。1912年後藤经过多次病理检查,倡用进行性骨化性肌膜增殖症之名。以后宫崎、浦上等,详细报告了有关本症的病理解剖,到目前为止国内外文献尚不满200例。国内有关本症的报导甚少。
Progressive multiple ossification myositis, is a frequent in young children, continuous or intermittent so that arbitrary muscle, muscle, tendon, tendon periosteum, ligaments and other occurrence of ossification, and finally the whole body into a stiff disease. Freke first reported in 1740 abroad. 1858 Muenchmyer reported 18 cases and analyzed. Stempell analyzed 44 articles in 1898. After 1912 vine after many pathological examination, advocating the name of progressive ossification of sarcoidosis. After Miyazaki, Uematsu, etc., detailed report about the pathological anatomy of the disease, so far at home and abroad, the literature is still less than 200 cases. Domestic reports of this disease is rare.