Zhang Zai-qiang, Sun Yi-lin, Niu Song-tao, Liang Xian-hong, Wang Yong-jun
Department of Neurology, Tiantan Hospital, Capital Medical University, Beijing 100050, China.
Zhonghua Yi Xue Za Zhi. 2009 May 5;89(17):1185-8.
To investigate the ultrastructural features of mitochondrial cytopathies and its diagnostic value.
Muscle biopsy specimens from 33 cases of mitochondrial cytopathies were examined by routine pathological and electron microscopic examinations.
The main pathologic changes included ragged red fibers in modified Gomori staining, hyper-intense staining myofibers in SDH, COX-negative fibers while dark counterstaining with SDH in COX/SDH double staining technique. Ultrastructural findings included subsarcolemmal and intramyofibrillar proliferation of mitochondria and the appearance of abnormal mitochondria, paracrystalline inclusions, concentric dystrophic cristae and excessive subsarcolemmal glycolipid compounds in subsarcolemmal.
The presence of proliferation and abnormality of mitochondria, electro-dense granule and paracrystalline inclusions in mitochondria provide key diagnostic evidence for the diagnosis of this disease.
探讨线粒体细胞病的超微结构特征及其诊断价值。
对33例线粒体细胞病患者的肌肉活检标本进行常规病理及电子显微镜检查。
主要病理改变包括改良Gomori染色可见破碎红纤维,琥珀酸脱氢酶(SDH)染色可见肌纤维强阳性染色,细胞色素氧化酶(COX)/SDH双重染色技术中COX阴性纤维而SDH呈深色复染。超微结构表现为肌膜下和肌原纤维内线粒体增生,出现异常线粒体、副结晶包涵体、同心性营养不良嵴以及肌膜下过量的肌膜下糖脂化合物。
线粒体的增生和异常、电子致密颗粒以及线粒体副结晶包涵体的存在为该病的诊断提供了关键诊断依据。