Jongpiputvanich Sungkom, Norapucsunton Terasak, Shuangshoti Shanop
Department of Pediatrics, Faculty of Medicine, Chulalongkorn University, Bangkok 10330, Thailand.
J Med Assoc Thai. 2004 Sep;87 Suppl 2:S55-8.
The authors retrospectively studied histopathologic findings and diagnoses of muscle specimens taken from 188 pediatric patients presenting with clinical neuromuscular disorders in King Chulalongkorn Memorial Hospital between August 1991 and December 2003. Eighty patients (67.8%) established the definite diagnosis by histopathological findings of muscle specimens. About 18.6, 17.7, 7.6, 5.9, 5.0, 3.4, 2.5 and 1.7 percent of the total number of patients were diagnosed as Duchenne muscular dystrophy, spinal muscular atrophy, congenital myopathies, mitochondrial disease, inflammatory myopathies, Becker muscular dystrophy, congenital muscular dystrophy and vacuolar myopathies respectively. Since the histopathological findings in muscle helped to establish the definite diagnosis in most pediatric patients in the present study, thus muscle biopsy is essential for establishing a definite diagnosis in any patient with a suspected neuromuscular disorder.
作者回顾性研究了1991年8月至2003年12月期间在朱拉隆功国王纪念医院就诊的188例患有临床神经肌肉疾病的儿科患者的肌肉标本的组织病理学发现和诊断。80例患者(67.8%)通过肌肉标本的组织病理学发现确诊。患者总数中分别有18.6%、17.7%、7.6%、5.9%、5.0%、3.4%、2.5%和1.7%被诊断为杜氏肌营养不良症、脊髓性肌萎缩症、先天性肌病、线粒体疾病、炎性肌病、贝氏肌营养不良症、先天性肌营养不良症和空泡性肌病。由于本研究中肌肉的组织病理学发现有助于大多数儿科患者确诊,因此肌肉活检对于任何疑似神经肌肉疾病的患者确诊至关重要。