Dhamala Ijan, Bhatta Soniya, Katel Dik P, Acharya Manish, Bashyal Krishnaprasad
Cardiothoracic and Vascular Surgery, Kathmandu Medical College, Kathmandu, NPL.
Anesthesia, All India Institute of Medical Sciences, Rishikesh, IND.
Cureus. 2025 Jul 19;17(7):e88279. doi: 10.7759/cureus.88279. eCollection 2025 Jul.
Arteriovenous malformations (AVMs) are rare congenital vascular anomalies characterized by direct connections between arteries and veins without intervening capillary beds, resulting in high-flow dynamics. While AVMs commonly affect the craniofacial region and extremities, involvement of the chest wall is exceedingly rare. We describe the case of a 19-year-old male patient who had a painless, progressively enlarging swelling in the right posterior chest wall that had been present since birth. Magnetic resonance imaging revealed a large, high-signal lesion involving subcutaneous and muscular planes of the right posterior chest wall, while computed tomography angiography demonstrated arterial feeders arising from multiple intercostal arteries, confirming the diagnosis of a high-flow AVM. A multidisciplinary approach was employed, beginning with fluoroscopy-guided embolization using polyvinyl alcohol particles and Gelfoam to devascularize the lesion. The patient had a successful en bloc surgical excision performed under general anesthesia one week later. Postoperative recovery was uneventful, and no recurrence was noted at six-month follow-up. This case underscores the importance of a staged, image-guided, and multidisciplinary treatment strategy in managing large, high-flow AVMs in rare anatomical locations such as the chest wall.
动静脉畸形(AVM)是一种罕见的先天性血管异常,其特征是动脉和静脉之间直接相连,中间没有毛细血管床,导致血流动力学呈高流量状态。虽然AVM通常影响颅面部区域和四肢,但胸壁受累极为罕见。我们描述了一例19岁男性患者的病例,该患者自出生以来右后胸壁就有一个无痛、逐渐增大的肿块。磁共振成像显示右后胸壁皮下和肌肉层面有一个大的高信号病变,而计算机断层血管造影显示有多条肋间动脉发出的动脉供血支,确诊为高流量AVM。采用了多学科方法,首先在荧光透视引导下使用聚乙烯醇颗粒和明胶海绵进行栓塞,使病变血管化。一周后,患者在全身麻醉下成功进行了整块手术切除。术后恢复顺利,六个月随访时未发现复发。该病例强调了在处理胸壁等罕见解剖部位的大型高流量AVM时,采用分阶段、影像引导和多学科治疗策略的重要性。