足月新生儿先天性喉狭窄伴出生缺陷1例报告。

Biomedicine Hub Pub Date : 2020-07-13 eCollection Date: 2020-05-01 DOI:10.1159/000508731
Patrycja Tesmer, Katarzyna Wróblewska-Seniuk, Jan Mazela, Jarosław Szydłowski
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引用次数: 0

摘要

先天性喉狭窄是一种罕见且不寻常的异常,通常在分娩后的头几分钟出现严重危及生命的呼吸窘迫。它可能作为一个孤立的实体存在,也可能与其他先天性畸形,特别是心脏异常有关。在本文中,我们提出的情况下,一个婴儿与产前怀疑法洛四联症。分娩后,患者立即要求插管,这证明是困难的。他最终被诊断为喉狭窄,需要喉科治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Congenital Laryngeal Stenosis and Concomitant Birth Defects in a Term Newborn: A Case Report.

Congenital laryngeal stenosis is a rare and unusual anomaly that usually presents in the first minutes after delivery as severe life-threatening respiratory distress. It may exist as an isolated entity or in association with other congenital malformations, in particular cardiac anomalies. In this paper, we present the case of an infant with prenatal suspicion of tetralogy of Fallot. Immediately after delivery, the patient required intubation, which proved difficult. He was eventually diagnosed with laryngeal stenosis requiring laryngological treatment.

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