A Rare Tumor of Nasal Cavity: Glomangiopericytoma

Glomangiopericytoma is a rare vascular neoplasm characterized by a pattern of prominent perivascular growth. A 72-year-old woman was admitted to our clinic complaining of nasal obstruction, frequent epistaxis, and facial pain. A reddish tumor filling the left nasal cavity was observed on endoscopy...

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Main Authors: Aysegul Verim, Cigdem Kalaycik Ertugay, Cigdem Tepe Karaca, Pembegul Gunes, Shahrouz Sheidaei, Cagatay Oysu
Format: Article
Language:English
Published: Wiley 2014-01-01
Series:Case Reports in Otolaryngology
Online Access:http://dx.doi.org/10.1155/2014/282958
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author Aysegul Verim
Cigdem Kalaycik Ertugay
Cigdem Tepe Karaca
Pembegul Gunes
Shahrouz Sheidaei
Cagatay Oysu
author_facet Aysegul Verim
Cigdem Kalaycik Ertugay
Cigdem Tepe Karaca
Pembegul Gunes
Shahrouz Sheidaei
Cagatay Oysu
author_sort Aysegul Verim
collection DOAJ
description Glomangiopericytoma is a rare vascular neoplasm characterized by a pattern of prominent perivascular growth. A 72-year-old woman was admitted to our clinic complaining of nasal obstruction, frequent epistaxis, and facial pain. A reddish tumor filling the left nasal cavity was observed on endoscopy and treated with endoscopic excision. Microscopically, closely packed cells interspersed with numerous thin-walled, branching staghorn vessels were seen. Glomangiopericytoma is categorized as a borderline low malignancy tumor by WHO classification. Long-term follow-up with systemic examination is necessary due to high risk of recurrence.
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institution Kabale University
issn 2090-6765
2090-6773
language English
publishDate 2014-01-01
publisher Wiley
record_format Article
series Case Reports in Otolaryngology
spelling doaj-art-1dcb154faf5a4e8ba984a3093efb24292025-02-03T01:01:04ZengWileyCase Reports in Otolaryngology2090-67652090-67732014-01-01201410.1155/2014/282958282958A Rare Tumor of Nasal Cavity: GlomangiopericytomaAysegul Verim0Cigdem Kalaycik Ertugay1Cigdem Tepe Karaca2Pembegul Gunes3Shahrouz Sheidaei4Cagatay Oysu5Department of Otorhinolaryngology/Head and Neck Surgery, Haydarpasa Numune Education and Research Hospital, 34668 Istanbul, TurkeyDepartment of Otorhinolaryngology/Head and Neck Surgery, Istanbul Hospital, Baskent University, Kulak Burun Boğaz Kliniği, Altunizade, Mahir İz Caddesi No. 43, 34662 Istanbul, TurkeyDepartment of Otorhinolaryngology/Head and Neck Surgery, Haydarpasa Numune Education and Research Hospital, 34668 Istanbul, TurkeyDepartment of Pathology, Haydarpasa Numune Education and Research Hospital, 34668 Istanbul, TurkeyDepartment of Otorhinolaryngology/Head and Neck Surgery, Haydarpasa Numune Education and Research Hospital, 34668 Istanbul, TurkeyDepartment of Otorhinolaryngology/Head and Neck Surgery, Haydarpasa Numune Education and Research Hospital, 34668 Istanbul, TurkeyGlomangiopericytoma is a rare vascular neoplasm characterized by a pattern of prominent perivascular growth. A 72-year-old woman was admitted to our clinic complaining of nasal obstruction, frequent epistaxis, and facial pain. A reddish tumor filling the left nasal cavity was observed on endoscopy and treated with endoscopic excision. Microscopically, closely packed cells interspersed with numerous thin-walled, branching staghorn vessels were seen. Glomangiopericytoma is categorized as a borderline low malignancy tumor by WHO classification. Long-term follow-up with systemic examination is necessary due to high risk of recurrence.http://dx.doi.org/10.1155/2014/282958
spellingShingle Aysegul Verim
Cigdem Kalaycik Ertugay
Cigdem Tepe Karaca
Pembegul Gunes
Shahrouz Sheidaei
Cagatay Oysu
A Rare Tumor of Nasal Cavity: Glomangiopericytoma
Case Reports in Otolaryngology
title A Rare Tumor of Nasal Cavity: Glomangiopericytoma
title_full A Rare Tumor of Nasal Cavity: Glomangiopericytoma
title_fullStr A Rare Tumor of Nasal Cavity: Glomangiopericytoma
title_full_unstemmed A Rare Tumor of Nasal Cavity: Glomangiopericytoma
title_short A Rare Tumor of Nasal Cavity: Glomangiopericytoma
title_sort rare tumor of nasal cavity glomangiopericytoma
url http://dx.doi.org/10.1155/2014/282958
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