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儿童耳周瘘管的临床形态学特征及治疗特点

Clinical-morphological characteristics and peculiarities of treatment of paraururicular fistulas in children.

作者信息

Tkachenko Pavlo I, Starchenko Ivan I, Bilokon Serhii O, Popelo Yuliia V, Lokhmatova Nataliia M, Dolenko Olha B, Korotych Nataliia M, Hohol Andrii M, Bilokon Nataliia P

机构信息

Ukrainian Medical Stomatological Academy, Poltava, Ukraine.

出版信息

Wiad Lek. 2020;73(6):1184-1188.

Abstract

OBJECTIVE

The aim: Determining the frequency of occurrence of paraauricular fistula in children and comparing the results of their own experience regarding their clinical manifestations, treatment principles and morphological features with existing scientific data.

PATIENTS AND METHODS

Materials and methods: The results of a comprehensive examination and surgical treatment of 25 children with paraauricular fistulas.

RESULTS

Results: Most often, para-auricular fistula was observed in infants 22 - (88%). In 18 persons (72%), they were unilateral, in 10 - (40%) hereditary. In 8 - (32%), fistula was diagnosed immediately after birth. In 17 - (68%) the pathology was not clinically manifested, but was an accidental finding during the next medical examination. Morphological research has shown that congenital paraauricular fistula is a formed canal intimately associated with the epithelium and cartilage, and the presence of epithelial lining on the fistula wall with constant support of the inflammatory process makes it impossible to heal even against the background of multicomponent treatment.

CONCLUSION

Conclusions: Due to the topographic-anatomical localization, features of the clinic of the born fistula, surgical treatment does not always allow to achieve the desired results, and requires repeated interventions during recurrence. It is possible to prevent recurrence by the extensive use of additional diagnostic manipulations before surgery and careful wound control during surgical procedures.

摘要

目的

确定儿童耳前瘘管的发生率,并将自身关于其临床表现、治疗原则和形态学特征的经验结果与现有科学数据进行比较。

患者与方法

材料与方法:对25例耳前瘘管患儿进行全面检查和手术治疗的结果。

结果

结果:耳前瘘管最常出现在婴儿中,共22例(88%)。18例(72%)为单侧,10例(40%)有遗传因素。8例(32%)在出生后立即被诊断出瘘管。17例(68%)的病变在临床上未表现出来,而是在下次体检时意外发现的。形态学研究表明,先天性耳前瘘管是一条与上皮和软骨紧密相连的形成管道,瘘管壁上存在上皮衬里并持续受到炎症过程的支持,即使在多组分治疗的背景下也无法愈合。

结论

结论:由于其局部解剖定位、先天性瘘管临床特征,手术治疗并不总能达到预期效果,复发时需要重复干预。通过在手术前广泛使用额外的诊断操作以及在手术过程中仔细控制伤口,可以预防复发。

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