Congenital Complete Tracheal Ring in a Neonate: A Case Report
Autor: | Esra Arun Ozer, Suheyla Cumurcu, Senem Alkan Özdemir, Sumer Sutcuoglu, Ozkan Ilhan, Umit Bayol |
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Jazyk: | angličtina |
Rok vydání: | 2017 |
Předmět: |
Heart Defects
Congenital medicine.medical_specialty Respiratory distress syndrome medicine.medical_treatment Tracheal stenosis Limb Deformities Congenital Anal Canal Kidney Pathology and Forensic Medicine Encephalocele VACTERL association Esophagus medicine lcsh:Pathology Humans Respiratory distress business.industry Infant Newborn Airway obstruction respiratory system medicine.disease Newborn Spine Surgery Trachea medicine.anatomical_structure Agenesis Airway management Airway business Respiratory tract lcsh:RB1-214 |
Zdroj: | Türk Patoloji Dergisi, Vol 33, Iss 3, Pp 259-261 (2017) |
ISSN: | 1309-5730 1018-5615 |
Popis: | Abnormalities of the upper airway tract lead to congenital high airway obstruction and may complicate neonatal airway management in the delivery room. Congenital complete tracheal rings are a rare and unusual tracheal anomaly, usually presenting in the neonate or infant as respiratory distress. The clinical presentation can vary from almost asymptomatic patients to near-fatal airway obstruction. It may exist as an isolated entity, or in association with other congenital malformations, in particular, cardiac anomalies along with vascular rings and pulmonary slings. Other associated anomalies have also been reported, for example, chromosomal anomalies, malformation of other parts of the respiratory tract, esophagus and skeletal systems. Here, we report an extreme case of VACTERL/TACRD association presented with congenital complete tracheal ring, encephalocele, bilateral radial agenesis with absent thumbs, equinovalgus deformity on right foot, low-set ears and micrognathia. |
Databáze: | OpenAIRE |
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