Mooney M P, Siegel M I, Kimes K R, Todhunter J
Department of Anthropology, University of Pittsburgh, Pa.
Plast Reconstr Surg. 1988 Mar;81(3):336-45. doi: 10.1097/00006534-198803000-00004.
As part of an ongoing study of cleft lip and palate fetal morphology, normal and dysmorphic development of the human fetal orbicularis oris muscle was studied in a cross-sectional sample of 29 human fetuses (20 "normal" and 9 cleft lip and palate) ranging in age from 8 to 21 postmenstrual weeks. The specimens were embedded in celloidin and sectioned at 20 microns, and every tenth section was stained with hematoxylin and eosin. A computer reconstruction technique was applied to produce three-dimensional representations of the orbicularis oris muscle. The orbicularis oris muscle in the normal fetal sample with discernible lip fibers (N = 15) increased symmetrically in both fiber density and complexity from 12 to 21 weeks. Metrically, muscle volume and thickness growth curves were consistent with qualitative observations. In contrast, the unilateral cleft lip and palate fetal specimens with discernible lip fibers (N = 3) exhibited a 3.5-week delay in overall muscle development, asymmetrical fiber distribution, and abnormal fiber insertions. However, quantitatively, no significant (p greater than 0.05) differences were noted in orbicularis oris muscle thickness or volume between the normal and cleft lip and palate fetal specimens through 21 weeks. Findings suggest that orbicularis muscle deficiency, noted clinically in cleft lip and palate neonates, may be a result of perinatal functional dysmorphogenesis rather than congenital mesenchymal reduction or deficiency.
作为一项正在进行的唇腭裂胎儿形态学研究的一部分,在29例人类胎儿(20例“正常”胎儿和9例唇腭裂胎儿)的横断面样本中,研究了人类胎儿口轮匝肌的正常和畸形发育情况,这些胎儿的孕周为8至21周。标本用火棉胶包埋,切成20微米厚的切片,每隔十张切片用苏木精和伊红染色。应用计算机重建技术生成口轮匝肌的三维图像。在具有可识别唇部纤维的正常胎儿样本(N = 15)中,口轮匝肌的纤维密度和复杂性从12周龄到21周龄均呈对称增加。从测量学角度来看,肌肉体积和厚度的生长曲线与定性观察结果一致。相比之下,具有可识别唇部纤维的单侧唇腭裂胎儿标本(N = 3)在整体肌肉发育上延迟了3.5周,纤维分布不对称,且纤维插入异常。然而,在21周龄之前,正常胎儿标本与唇腭裂胎儿标本的口轮匝肌厚度或体积在定量上没有显著差异(p大于0.05)。研究结果表明,临床上在唇腭裂新生儿中观察到的口轮匝肌缺陷可能是围产期功能发育异常的结果,而非先天性间充质减少或缺陷。