| Literature DB >> 12176189 |
O Gazi Yigitbasi1, Gulen Guler, Figen Ozturk, Ercihan Guney.
Abstract
Glandular hamartoma of the larynx is an extremely rare lesion, and the number of well-documented and acceptable cases is limited. Presenting symptoms may include changes in voice, eating and activity levels, and respiratory complaints. We report on a 14-month-old infant with this rare clinical entity. Direct laryngoscopy revealed a well-mucosalized, encapsulated, firm, 0.5 cm wide and 2.5 cm long lesion that originated from the right aryepiglottic fold and reached into the nasopharynx. The mass was completely excised endoscopically. Histopathological examination revealed a hamartoma, which was composed of glandular elements, mixed with mesodermal tissues. After endoscopic removal of the hamartoma, the child was relieved of the obstruction. Copyright 2002 Elsevier Science Ireland Ltd.Entities:
Mesh:
Year: 2002 PMID: 12176189 DOI: 10.1016/s0165-5876(02)00150-7
Source DB: PubMed Journal: Int J Pediatr Otorhinolaryngol ISSN: 0165-5876 Impact factor: 1.675