Department of Pathology, Seth GS Medical College, Mumbai, Maharashtra, India.
Department of Cardiac Surgery, Boston Children's Hospital/Harvard Medical School, Boston, MA, USA.
Indian J Pathol Microbiol. 2021 Oct-Dec;64(4):683-686. doi: 10.4103/IJPM.IJPM_363_20.
The "Ring-and-Sling" complex (RSC) comprises congenital tracheal stenosis and an abnormal origin/course of the left pulmonary artery. Based on clinical and imaging studies, the luminal narrowing is assumed to be as a result of rings cartilage (forming an "O").
This is a postmortem based study of tracheal histology in infants after an autopsy encounter of a case of RSC.
RSC was identified in an infant at autopsy. The tracheal histomorphology revealed the presence of cartilaginous plates (instead of rings) and fibro-elastotic proliferation at the site of trachealis muscle. These changes prompted a study on variations in the histology of the trachea (with no known anomaly) in 35 autopsied neonates and infants. The transverse sections of the trachea were taken at one or more levels (Level 1 - at the level of the thyroid, Level 2 - midway between the thyroid and the carina, and Level 3 - just above the carina.
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On histology, 83 sections showed the trachealis muscle on the posterior aspect. A single semicircular cartilage was identified in only 17 of the 83 sections studied (20.5%, 6 in level 1, 9 in level 2 and 2 in level 3). In the remaining 66 sections (79.5%), the cartilage was disposed as multiple plates, ranging in number from 2 to 10. No significant association was found between semicircular cartilage rings and age, sex, gestational age, and level of section (P < 0.05). However, 14 cases with sectioning at all three levels were taken into account; all levels showed more cartilaginous plates compared to single rings, which were more common at level 1 (P > 0.05).
The "ring" in RSC and normal infantile tracheas show cartilage plates with intermittent semicircular cartilage rings. These findings may have surgical implications for tracheal anomalies and bode favorable surgical outcomes.
“环带吊带”(RSC)复合体包括先天性气管狭窄和左肺动脉异常起源/走行。基于临床和影像学研究,管腔狭窄被认为是由于环状软骨(形成“O”形)。
这是一项基于尸检的 RSC 病例的婴儿气管组织学研究。
在尸检中发现 RSC 婴儿。气管组织形态学显示气管平滑肌有软骨板(而非环状)和纤维弹性增生。这些变化促使我们研究 35 例尸检新生儿和婴儿的气管组织学(无已知异常)的变化。在一个或多个水平取气管的横切面(水平 1-甲状腺水平,水平 2-甲状腺和隆突之间的中间,水平 3-隆突上方)。
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在组织学上,83 个切片显示气管后壁有气管平滑肌。在 83 个研究切片中,只有 17 个(20.5%,6 个在水平 1,9 个在水平 2,2 个在水平 3)显示单个半环状软骨。在其余 66 个切片(79.5%)中,软骨呈多个板状排列,数量从 2 到 10 不等。半环状软骨环与年龄、性别、胎龄和切片水平之间无显著相关性(P<0.05)。然而,考虑到在所有三个水平上进行了 14 例切片,所有水平显示的软骨板比单个环状软骨多,而在水平 1 更常见(P>0.05)。
RSC 和正常婴儿气管中的“环”显示有软骨板和间歇性半环状软骨环。这些发现可能对气管异常有手术意义,并预示着良好的手术结果。