| Literature DB >> 19900773 |
Atsuko Furuta1, Mutsuo Kudo, Ken-ichi Kanai, Seido Ohki, Harumi Suzaki.
Abstract
Carcinoid tumors arise from neuroendocrine cells, many of which are present in the digestive tract and lungs. There have been few reports of carcinoid tumors occurring in the nose and paranasal sinus area, and they are very rare. We encountered a patient with a carcinoid tumor that arose in the nose and paranasal sinuses, and we report the case with a review of the literature. The patient was a 75-year-old woman who began to experience right-sided nasal obstruction, and when her nose began to bleed on the right-side she was examined in our department. A tumor lesion that easily bled and had filled the right nasal cavity was observed. CT revealed a mass lesion with a marked contrast enhancement in the right nasal cavity, ethmoid sinus, and sphenoid sinus, and MRI showed numerous flow voids in the interior that seemed to be tumor blood vessels. The tumor was excised through a lateral rhinotomy. The histopathological diagnosis was a carcinoid tumor. Tumor recurrence was subsequently detected in the vicinity of the opening of the sphenoid sinus, and because the tumor was tending to grow larger, the tumor was resected. The patient has been followed up in the outpatient clinic, recurrence-free. Copyright (c) 2009 Elsevier Ireland Ltd. All rights reserved.Entities:
Mesh:
Year: 2009 PMID: 19900773 DOI: 10.1016/j.anl.2009.09.007
Source DB: PubMed Journal: Auris Nasus Larynx ISSN: 0385-8146 Impact factor: 1.863