Coskun Berna Uslu, Sozen Esra, Basak Tulay, Alkan Seyhan, Dadas Burhan
Sisli Etfal Teaching and Training Hospital, Otorhinolaryngology Department, Istanbul, Turkey.
Int J Pediatr Otorhinolaryngol. 2005 Sep;69(9):1287-90. doi: 10.1016/j.ijporl.2005.03.050.
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.
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。
