Erdur Zülküf Burak, Yener Haydar Murat, Yilmaz Mehmet, Karaaltin Ayşegül Batioğlu, Inan Hakki Caner, Alaskarov Elvin, Gozen Emine Deniz
Department of Otolaryngology Head and Neck Surgery, Istanbul University Cerrahpasa School of Medicine, Istanbul, Turkey.
J Craniofac Surg. 2017 Nov;28(8):e720-e722. doi: 10.1097/SCS.0000000000003845.
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.
血管纤维瘤是鼻咽部常见的肿瘤,但细胞型在头颈部极为罕见。一名13岁男孩出现反复鼻出血和鼻塞6个月。根据临床症状和影像学检查,怀疑为青少年血管纤维瘤。在血管造影栓塞后,通过面中部脱套入路对病变进行了完整切除。组织学检查显示肿瘤由鹿角状血管和不规则纤维间质组成。在细胞丰富的间质中可见核小而固缩至大而泡状的星状成纤维细胞。这些发现确定为酷似青少年血管纤维瘤的细胞型血管纤维瘤。本文报道了一例非常罕见的鼻咽部细胞型血管纤维瘤患者。