Davis S, Bove K E, Wells T R, Hartsell B, Weinberg A, Gilbert E
Department of Pathology, Children's Hospital Medical Center, Cincinnati, Ohio 45229.
Pediatr Pathol. 1992 May-Jun;12(3):349-64. doi: 10.3109/15513819209023315.
Tracheal cartilaginous sleeve (TCS) is a rare congenital malformation in which discrete cartilaginous rings are replaced by a grossly uninterrupted cartilaginous sleeve. Seven previous patients with TCS have been reported in the world literature; in each instance, TCS was associated with craniosynostosis (CS). We report details of five additional patients with TCS, of whom four had a dominantly inherited CS. Gross examination of the available tracheas and bronchi demonstrates a cartilaginous sleeve with posterior interruption but lacking a normal pars membranacea. The stained and cleared tracheas all demonstrate variable ring formation, usually limited to the posterolateral aspect. The functional significance of TCS, if any, is unknown. No data are available on the prevalence of TCS in CS syndromes. The formation of TCS implies a common mesenchymal defect in which normally discrete structures fuse and is probably analogous to other mesenchymal abnormalities seen in these patients.
气管软骨套(TCS)是一种罕见的先天性畸形,其中离散的软骨环被一个明显不间断的软骨套所取代。世界文献中已报道了7例先前患有TCS的患者;在每个病例中,TCS都与颅缝早闭(CS)相关。我们报告了另外5例TCS患者的详细情况,其中4例具有显性遗传的CS。对可用气管和支气管的大体检查显示有一个软骨套,其后部中断,但缺乏正常的膜部。染色和透明处理后的气管均显示出不同程度的环状形成,通常局限于后外侧。TCS的功能意义(如果有)尚不清楚。关于CS综合征中TCS的患病率尚无数据。TCS的形成意味着一种常见的间充质缺陷,即正常离散的结构融合,可能类似于这些患者中出现的其他间充质异常。