Congenital midline cervical cleft (literature survey and description of own clinical observations)

O. Lukiianets, A. Sasiuk, V. Konoplitskyi, Ya.Yu. Marunkevych, K. Pedorenko
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Abstract

Midline cervical cleft - (synonym: webbed neck, pterygium colli medianum, neck ugliness), belongs to rare congenital defects which, unfortunately, have not been widely covered in the specialized medical literature at the modern stage of the development of medicine. It is confirmed by the fact that until 2014 according to the literature search there were a little over 100 detailed descriptions of the respective pathology. Purpose - to summarize the experience accumulated by experts in order to understand deeper all the aspects of Congenital midline cervical cleft, to introduce the present position of this rare congenital malformation to colleagues, to learn the structural parts of this pathology and the tactic for its treatment. The article represents the last data from scientific literature about Congenital midline cervical cleft and the analytic results of the two medical cases with this congenital malformation in children. Studying these cases, we used general clinical tests and histological research for the removal tissues. Conclusions. The current lack of information on the midline cervical cleft as well as the results of histological examinations in different clinical cases confirm the necessity of further study of this rare congenital defect. In this case, a deeper analysis of embryological, genetic and environmental factors influencing the process of formation of this pathology can be of help. In our opinion, performing the surgery becomes appropriate before two-year age in order to prevent the relapse of this pathology and severe neck contractures in the future. The study was carried out in accordance with the principles of the Helsinki declaration. The informed consent of the patient was obtained for conducting the studies. No conflict of interests was declared by the authors.
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先天性宫颈中线裂(文献综述及自身临床观察描述)
颈中线裂(同义:网状颈、中颈翼状胬肉、颈丑)是一种罕见的先天性缺陷,遗憾的是,在现代医学发展阶段,尚未在专业医学文献中广泛报道。事实证明,直到2014年,根据文献检索,有100多篇关于各自病理的详细描述。目的:总结专家积累的经验,以便更深入地了解先天性颈中线裂的各个方面,向同行介绍这种罕见的先天性畸形的目前位置,了解这种病理的结构部位及其治疗策略。本文介绍了有关先天性颈中线裂的最新科学文献资料和对两例小儿先天性畸形的分析结果。研究这些病例,我们使用一般临床检查和组织学研究的切除组织。结论。目前关于宫颈中线裂的资料缺乏以及不同临床病例的组织学检查结果证实了对这种罕见先天性缺陷进行进一步研究的必要性。在这种情况下,更深入地分析影响这种病理形成过程的胚胎学、遗传和环境因素可能会有所帮助。我们认为,在两岁之前进行手术是合适的,以防止这种病理复发和将来严重的颈部挛缩。这项研究是按照《赫尔辛基宣言》的原则进行的。获得患者的知情同意进行研究。作者未声明存在利益冲突。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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