Literature DB >> 9793982

Laryngeal atresia or stenosis presenting as second-trimester fetal ascites--diagnosis and pathology in three independent cases.

P J Morrison1, S Macphail, D Williams, G McCusker, P McKeever, C Wright, N C Nevin.   

Abstract

Congenital atresia of the larynx is a rare abnormality. We describe three cases where prenatal diagnosis during the second trimester showed massive abdominal fetal ascites and at post-mortem, laryngeal atresia was identified in two cases, and severe laryngeal stenosis in the third. All were associated with pulmonary hyperplasia. No additional abnormalities were found in other systems. Overdistended lung tissue and ascites are resultant from aberrant laryngeal growth; laryngeal anomalies are a cause of isolated fetal ascites. The association of ascites and voluminous lungs should arouse suspicion of laryngeal atresia and should be an indication for careful pathological study of the fetal larynx.

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Year:  1998        PMID: 9793982

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  2 in total

1.  Prenatal detection of congenital high airway obstruction syndrome with encephalocele.

Authors:  Laxmi Devi Padmanabhan; Sheela Nampoothiri
Journal:  Indian J Radiol Imaging       Date:  2016 Jan-Mar

2.  Case report: Antenatal diagnosis of congenital high airway obstruction syndrome - laryngeal atresia.

Authors:  Mukesh Kumar Garg
Journal:  Indian J Radiol Imaging       Date:  2008-11
  2 in total

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