Affiliations 

  • 1 Department of Otolaryngology-Head & Neck Surgery, Faculty of Medicine, International Islamic, University Malaysia
  • 2 Department of Radioimaging, Tengku Ampuan Afzan Hospital, Kuantan, Malaysia
Med J Malaysia, 2006 Dec;61(5):644-6.
PMID: 17623972 MyJurnal

Abstract

Intranasal haemangioma is quite rare. This tumor may be confused with other intranasal vascular tumor such as juvenile nasopharyngeal angiofibroma (JNA), glomus tumors as well as other tumor such as angiosarcoma and leiomyoma. Juvenile nasopharyngeal angiofibroma is the most common vascular tumor encountered in nasal cavity. A definitive histology diagnosis pre-operatively is difficult to be obtained as the biopsy may lead into severe uncontrolled bleeding. The final diagnosis very much depends on histology after the tumor excision. Complete surgical resection of the tumor is the standard approach. In this report we describe our surgical management in approaching intranasal haemangioma endoscopically and this pathology can be considered as one of differential diagnosis for unilateral nasal mass.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.