We describe the case of a boy with spondyloepiphyseal dysplasia congenita. At birth, he experienced severe respiratory distress necessitating tracheotomy. Endoscopy done because mechanical ventilation failed to resolve desaturations disclosed severe tracheo-bronchomalacia. A Polyflex silicone stent was placed in the trachea (replaced by Y-Dumon stent) and 2 Palmaz metallic stents in the mainstem bronchi (overlapped with 2 Jomed stents 5 years later). Airway stenting guaranteed a suitable respiratory status and allowed a child who was expected to die at birth, to reach 13.5 years old in good conditions.
Airway stenting in a child with spondyloepiphyseal dysplasia congenita: 13-Year survival / Nenna, R., Midulla, F., Masi, L., Bacci, G.M., Frassanito, A., Baggi, R., Brandi, M.L., Avenali, S., Mirabile, L., Serio, P.. - In: INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY. - ISSN 1872-8464. - ELETTRONICO. - 99:(2017), pp. 13-16. [10.1016/j.ijporl.2017.05.008]
Airway stenting in a child with spondyloepiphyseal dysplasia congenita: 13-Year survival.
BACCI, GIACOMO MARIA;FRASSANITO, ANNA;BRANDI, MARIA LUISA;
2017
Abstract
We describe the case of a boy with spondyloepiphyseal dysplasia congenita. At birth, he experienced severe respiratory distress necessitating tracheotomy. Endoscopy done because mechanical ventilation failed to resolve desaturations disclosed severe tracheo-bronchomalacia. A Polyflex silicone stent was placed in the trachea (replaced by Y-Dumon stent) and 2 Palmaz metallic stents in the mainstem bronchi (overlapped with 2 Jomed stents 5 years later). Airway stenting guaranteed a suitable respiratory status and allowed a child who was expected to die at birth, to reach 13.5 years old in good conditions.| File | Dimensione | Formato | |
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