| Literature DB >> 27146659 |
Pinar Kendigelen1, Yusuf Tunali2, Ayse Tutuncu2, Gulruh Ashyralyyeva2, Senol Emre3, Guner Kaya2.
Abstract
The mucopolysaccharidosis (MPS) is a rare lysosomal storage disease. Glycosaminoglycans (GAG) accumulate in musculoskeletal system, connective tissues. Enlarged tongue, short immobile neck, and limited mobility of the cervical spine and temporomandibular joints render the airway management potentially risky. MPS children have high anesthetic risks, especially in airway management of emergency situations. The foreign-body aspiration requiring intervention with rigid bronchoscopy is an urgent and risky clinical situation. We present our experience with a challenging airway management with a three-year-old child with MPS who needed emergency bronchoscopy due to peanut aspiration.Entities:
Keywords: Airway management; Mucopolysaccharidosis; Sugammadex
Mesh:
Year: 2016 PMID: 27146659 DOI: 10.1007/s00540-016-2180-7
Source DB: PubMed Journal: J Anesth ISSN: 0913-8668 Impact factor: 2.078