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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Format: | Article |
Language: | English |
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Wiley
2014-01-01
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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. |
format | Article |
id | doaj-art-1dcb154faf5a4e8ba984a3093efb2429 |
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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