Cellular Angiofibroma of the Nasopharynx
Angiofibroma is a common tumor of the nasopharynx region but cellular type is extremely rare in head and neck. A 13-year-old boy presented with frequent epistaxis and nasal obstruction persisting for 6 months. According to the clinical symptoms and imaging studies juvenile angiofibroma was suspected...
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Veröffentlicht in: | The Journal of craniofacial surgery 2017-11, Vol.28 (8), p.e720-e722 |
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container_title | The Journal of craniofacial surgery |
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creator | Erdur, Zülküf Burak Yener, Haydar Murat Yilmaz, Mehmet Karaaltin, Ayşegül Batioğlu Inan, Hakki Caner Alaskarov, Elvin Gozen, Emine Deniz |
description | Angiofibroma is a common tumor of the nasopharynx region but cellular type is extremely rare in head and neck. A 13-year-old boy presented with frequent epistaxis and nasal obstruction persisting for 6 months. According to the clinical symptoms and imaging studies juvenile angiofibroma was suspected. Following angiographic embolization total excision of the lesion by midfacial degloving approach was performed. Histological examination revealed that the tumor consisted of staghorn blood vessels and irregular fibrous stroma. Stellate fibroblasts with small pyknotic to large vesicular nuclei were seen in a highly cellular stroma. These findings identified cellular angiofibroma mimicking juvenile angiofibroma. This article is about a very rare patient of cellular angiofibroma of nasopharynx. |
doi_str_mv | 10.1097/SCS.0000000000003845 |
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A 13-year-old boy presented with frequent epistaxis and nasal obstruction persisting for 6 months. According to the clinical symptoms and imaging studies juvenile angiofibroma was suspected. Following angiographic embolization total excision of the lesion by midfacial degloving approach was performed. Histological examination revealed that the tumor consisted of staghorn blood vessels and irregular fibrous stroma. Stellate fibroblasts with small pyknotic to large vesicular nuclei were seen in a highly cellular stroma. These findings identified cellular angiofibroma mimicking juvenile angiofibroma. 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A 13-year-old boy presented with frequent epistaxis and nasal obstruction persisting for 6 months. According to the clinical symptoms and imaging studies juvenile angiofibroma was suspected. Following angiographic embolization total excision of the lesion by midfacial degloving approach was performed. Histological examination revealed that the tumor consisted of staghorn blood vessels and irregular fibrous stroma. Stellate fibroblasts with small pyknotic to large vesicular nuclei were seen in a highly cellular stroma. These findings identified cellular angiofibroma mimicking juvenile angiofibroma. 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subjects | Adolescent Angiofibroma - pathology Angiofibroma - physiopathology Angiofibroma - surgery Angiography - methods Dentistry Embolization, Therapeutic - methods Epistaxis - diagnosis Epistaxis - etiology Humans Male Nasal Obstruction - diagnosis Nasal Obstruction - etiology Nasopharyngeal Neoplasms - pathology Nasopharyngeal Neoplasms - physiopathology Nasopharyngeal Neoplasms - surgery Nasopharynx - blood supply Nasopharynx - diagnostic imaging Nasopharynx - surgery Neck Dissection - methods Treatment Outcome |
title | Cellular Angiofibroma of the Nasopharynx |
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