Abstract
References
- 1. Buckmire RA, Kwon TK. Bilateral obstructing laryngeal epithelial adenomatous hamartomas. Arch Otolaryngol Head Neck Surg 2005;131:259-61. [CrossRef]
- 2. Daniel SJ. The upper airway congenital malformations. Paediatr Respir Rev 2006;7:260-3. [CrossRef]
- 3. Fine ED, Dahmas B, Arnold JE. Laryngeal hamartoma: A rare congenital abnormality. Ann Otol Rhinol Laryngol 1995;104:87-9. [CrossRef]
- 4. Karatas E, Mumbuc S, Durucu C, Kanlıkama M, Bakır K, Ekiz S. Hamartoma of the larynx causing nonspesifik symptoms in the falce vocal cord: Original image. Turkiye Klinikleri J Med Sci 2008;28:252-4.
- 5. Leung AK, Cho HY. Diagnosis of stridor in children. Am Fam Physician 1999;60:2289-96.
- 6. Linder A. Hamartoma of the larynx causing neonatal respiratory distress. J Larygol Otol 1997;112:166-8.
- 7. Makitie AA, Lehtonen H, Back L, Aaltonen LM, Leivo I. Hamartoma of the larynx: An unusual cause of dyspnea. Ann Otol Rhinol Laryngol 2003;112:841-3. [CrossRef]
- 8. Rinaldo A, Mannara GM, Fisher C, Ferlito A. Hamartoma of the larynx: a critical review of the literature. Ann Otol Rhinol Laryngol 1998;107:264-7. [CrossRef]
- 9. Yigitbasi OG, Guler G, Ozturk F, Guney E. Glandular hamartoma of the larynx. Int J Pediatr Otorhinolaryngol 2002;65:163-6. [CrossRef]
Abstract
Background: Hamartoma of the larynx is a very rare lesion, and
the number of reported cases is limited. Signs and symptoms include
stridor, changes in voice, eating and respiratory complaints. Stridor
is a sign of upper airway obstruction. Patients presenting with stridor
and severe respiratory distress necessitate urgent otolaryngologic
evaluation.
Case Report: Herein, we report a case of laryngeal hamartoma presenting
with recurrent pneumonia and persistent stridor in a 7-monthold
patient. He was admitted to hospital with the initial diagnosis of recurrent pneumonia and persistent stridor. Stridor was not responsive
to cool mist, nebulised epinephrine or dexamethasone. Cervical computed
tomography (CT) revealed a solid, nodular mass on the posterolateral
wall of larynx. The mass was excised surgically. After surgical
removal of the hamartoma, the child was relieved of the obstruction.
Conclusion: We want to emphasise that patients presenting with persistent
stridor and severe distress necessitate urgent otolaryngologic
evaluation
Keywords
References
- 1. Buckmire RA, Kwon TK. Bilateral obstructing laryngeal epithelial adenomatous hamartomas. Arch Otolaryngol Head Neck Surg 2005;131:259-61. [CrossRef]
- 2. Daniel SJ. The upper airway congenital malformations. Paediatr Respir Rev 2006;7:260-3. [CrossRef]
- 3. Fine ED, Dahmas B, Arnold JE. Laryngeal hamartoma: A rare congenital abnormality. Ann Otol Rhinol Laryngol 1995;104:87-9. [CrossRef]
- 4. Karatas E, Mumbuc S, Durucu C, Kanlıkama M, Bakır K, Ekiz S. Hamartoma of the larynx causing nonspesifik symptoms in the falce vocal cord: Original image. Turkiye Klinikleri J Med Sci 2008;28:252-4.
- 5. Leung AK, Cho HY. Diagnosis of stridor in children. Am Fam Physician 1999;60:2289-96.
- 6. Linder A. Hamartoma of the larynx causing neonatal respiratory distress. J Larygol Otol 1997;112:166-8.
- 7. Makitie AA, Lehtonen H, Back L, Aaltonen LM, Leivo I. Hamartoma of the larynx: An unusual cause of dyspnea. Ann Otol Rhinol Laryngol 2003;112:841-3. [CrossRef]
- 8. Rinaldo A, Mannara GM, Fisher C, Ferlito A. Hamartoma of the larynx: a critical review of the literature. Ann Otol Rhinol Laryngol 1998;107:264-7. [CrossRef]
- 9. Yigitbasi OG, Guler G, Ozturk F, Guney E. Glandular hamartoma of the larynx. Int J Pediatr Otorhinolaryngol 2002;65:163-6. [CrossRef]
Details
| Other ID | JA32JP42UA |
|---|---|
| Journal Section | Research Article |
| Authors | |
| Publication Date | October 1, 2014 |
| Published in Issue | Year 2014 Volume: 31 Issue: 4 |