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先天性气管狭窄中完全性气管环的组织学特征。

Histological features of complete tracheal rings in congenital tracheal stenosis.

机构信息

Department of Pediatric Surgery, Kobe Children's Hospital, 1-6-7, Minatojima Minami-cho, Chuo-ku, Kobe, 650-0047, Japan.

出版信息

Pediatr Surg Int. 2021 Feb;37(2):257-260. doi: 10.1007/s00383-020-04803-z. Epub 2021 Jan 2.

Abstract

PURPOSE

Congenital tracheal stenosis is a disease in which complete tracheal cartilage rings (CTCR) cause airway narrowing. Although tracheal cartilage malformation has been suggested as a cause of CTCR, no histological studies have been performed. Here, we report a comparison of the tissues from CTCR and normal tracheal cartilage.

METHODS

Thirty-one infants who underwent slide tracheoplasty at our institution from May 2016 to August 2019 were included. Tissues from ten autopsy cases without tracheal lesions were used as controls. The survey items were tracheal cartilage cell density, cartilage thickness, and chondrocyte findings.

RESULTS

The median cartilage cell density from cases was 23/125 × 125 µm and from controls was 23.5/125 × 125 µm (p = 0.90). The median cartilage thickness from cases was 689 µm and from controls was 840 µm (p = 0.11). Comparing the ventral and dorsal sides of the CTCR tissues, the cell density was significantly different (median ventral 23/125 × 125 µm; median dorsal 19.5/125 × 125 µm; p = 0.034). There were no significant findings in the chondrocytes of the CTCR tissues.

CONCLUSION

CTCR tissues did not differ in cartilage density and thickness from normal tracheal cartilage.

摘要

目的

先天性气管狭窄是一种由完全性气管软骨环(CTCR)导致气道狭窄的疾病。虽然气管软骨畸形已被认为是 CTCR 的病因之一,但尚未进行组织学研究。在此,我们报告了 CTCR 与正常气管软骨组织的比较。

方法

纳入 2016 年 5 月至 2019 年 8 月在我院行滑动气管成形术的 31 例婴儿。将 10 例无气管病变的尸检组织作为对照。调查项目包括气管软骨细胞密度、软骨厚度和软骨细胞发现。

结果

病例的软骨细胞密度中位数为 23/125×125µm,对照组为 23.5/125×125µm(p=0.90)。病例的软骨厚度中位数为 689µm,对照组为 840µm(p=0.11)。比较 CTCR 组织的腹侧和背侧,细胞密度有显著差异(中位数腹侧 23/125×125µm;中位数背侧 19.5/125×125µm;p=0.034)。CTCR 组织的软骨细胞无明显异常。

结论

CTCR 组织的软骨密度和厚度与正常气管软骨无差异。

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