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鼻咽部动静脉畸形:一例报告

Arteriovenous malformation of the nasopharynx: a case report.

作者信息

Coskun Berna Uslu, Sozen Esra, Basak Tulay, Alkan Seyhan, Dadas Burhan

机构信息

Sisli Etfal Teaching and Training Hospital, Otorhinolaryngology Department, Istanbul, Turkey.

出版信息

Int J Pediatr Otorhinolaryngol. 2005 Sep;69(9):1287-90. doi: 10.1016/j.ijporl.2005.03.050.

Abstract

Arteriovenous malformation (AVM) of the head and neck is a rare vascular anomaly but when present is persistent and progressive in nature and can represent itself truly as a lethal benign disease. We present here an unusual case of an AVM with the size of 1.5 cm x 0.8 cm at the adenoid tissue found in an 8-year-old boy, which is not previously reported in the literature where we treated the patient with surgery alone. Although bleeding is a common presentation with vascular malformations, we have not seen any bleeding in our case. After the surgery, paranasal sinus and neck CT were undertaken. They showed no other AVM.

摘要

头颈部动静脉畸形(AVM)是一种罕见的血管异常,但一旦出现,其本质上具有持续性和进展性,可表现为一种真正的致命性良性疾病。我们在此报告一例不寻常的AVM病例,该病例发生在一名8岁男孩的腺样体组织中,大小为1.5厘米×0.8厘米,此前文献中未见报道,我们仅通过手术对该患者进行了治疗。尽管出血是血管畸形的常见表现,但我们的病例中未出现任何出血情况。手术后,进行了鼻窦和颈部CT检查。检查结果显示未发现其他AVM。

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