先天性单侧唇裂的软组织结构,光学和电子显微镜观察

Martin Zibrín, Marianna Zábavníková, Lenka Baňacká, Katarína Holovská, Peter Kizek, T. Komorová, Andrej Jenča
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引用次数: 0

摘要

唇裂(CL)、腭裂(CP)或两者均裂(CLP)是人类最常见的先天性畸形之一,给患者及其近亲造成了沉重的负担。我们对 7 名儿童的 CL 活检材料进行了研究:其中六名是 2 到 6 个月大的婴儿,一名是 4 岁的男孩。样本是在首次唇裂手术修复时采集的。光镜(LM)血红素和伊红染色的石蜡切片以及甲苯胺蓝染色的 0.5-1 μm 杜氏切片(用于透射电子显微镜(TEM))显示,所有七名儿童都有异常的 "锯齿状 "波浪形肌纤维。常规 TEM 证实了我们的结果;我们在 TEM 中没有发现软组织的其他变化;疏松结缔组织的血管和神经纤维正常。因此,我们认为唇裂肌纤维的病理变化不可能是神经元引起的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Structure of Soft Tissues in Congenital Unilateral Cleft Lip, Light and Electron Microscopic Observations
Cleft lip (CL), palate (CP), or both (CLP) are one of the most common congenital abnormalities in humans, causing a heavy burden to the affected and their next of kin. We examined biopsy material from CL of seven children: Six 2 to 6 month-old babies and one 4-year-old boy. The samples were taken at the first surgical cleft lip repair. Light microscopy (LM) haematoxylin and eosin stained paraffin sections and toluidine blue stained 0.5–1 μm Durcupan sections from material processed for transmission electron microscopy (TEM), revealed abnormal “ragged” wavy muscle fibres in all seven children. The routine TEM confirmed our results LM; we found no other changes in the soft tissues in TEM; blood vessels of loose connective tissue and nerve fibres were normal. Therefore, we believe that myopathic changes in the cleft lip muscle fibres cannot be of neuronal origin.
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