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[Laryngeal changes in mucoviscidosis]

J Tomik¹, E Kotarba

¹Kliniki Otolaryngologicznej CM UJ, Krakowie.

Otolaryngologia Polska = the Polish Otolaryngology

|January 1, 1994

Summary

Cystic fibrosis, a hereditary disease, rarely presents with laryngological symptoms. This study observed five children with cystic fibrosis, three with nasal polyps and two with recurrent parotid gland infections.

Area of Science:

Otolaryngology
Pediatrics
Genetics

Background:

Mucoviscidosis, also known as cystic fibrosis, is a congenital, hereditary disorder affecting exocrine glands.
Laryngological manifestations of cystic fibrosis are infrequently encountered in clinical practice.

Observation:

This study examined five pediatric patients diagnosed with cystic fibrosis.
Three patients underwent surgical intervention for nasal and paranasal sinus polyps.
Two patients were monitored for recurrent parotid gland infections.

Findings:

The case series highlights the occurrence of otolaryngological symptoms in pediatric cystic fibrosis patients.
Nasal polyposis and parotid gland infections represent potential clinical presentations.

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Implications:

Increased awareness of these laryngological symptoms may aid in earlier diagnosis and management of cystic fibrosis.
Further research is warranted to elucidate the specific mechanisms linking cystic fibrosis to these otolaryngological issues.