Mach Maciej, Ostrowski Tomasz, Giba Aleksandra, Sudol Natalia, Kabala Przemyslaw, Jakuczun Wawrzyniec, Maciąg Rafał, Sajdek Michał, Gałązka Zbigniew
Department of General, Vascular, Endocrine, and Transplant Surgery, Medical University of Warsaw, Warsaw, POL.
Department of Vascular Surgery, Samodzielny Publiczny Specjalistyczny Szpital Zachodni im. św. Jana Pawła II, Grodzisk Mazowiecki, POL.
Cureus. 2025 Jul 17;17(7):e88173. doi: 10.7759/cureus.88173. eCollection 2025 Jul.
We present the case of a 62-year-old woman with a history of long-standing, poorly controlled arterial hypertension, with average home blood pressure readings of approximately 140-160/100-110 mmHg despite treatment with ramipril, who was urgently admitted due to acute critical ischemia of the left lower limb. Imaging revealed an extensive Stanford type B aortic dissection (TBAD) involving the thoracoabdominal aorta and iliac arteries, with significantly impaired perfusion of the left leg. Due to the severity of limb ischemia and limitations to immediate endovascular repair, an urgent right-to-left femoro-femoral bypass was performed as a limb-saving procedure. Postoperatively, the patient developed multiorgan complications, including acute kidney injury (AKI) requiring hemodialysis and bowel ischemia, which were managed conservatively. The definitive repair of the dissection was achieved through thoracic endovascular aortic repair (TEVAR). Several weeks later, the patient presented with a gradually enlarging, painless, pulsatile mass in the right antecubital fossa, corresponding to a prior arterial access site. Clinical features, including a palpable thrill and audible bruit, were consistent with an iatrogenic arteriovenous fistula (AVF), which was surgically excised with the preservation of arterial flow and uneventful recovery. This case underscores the complex and life-threatening course of complicated type B aortic dissection with peripheral malperfusion, the necessity of staged hybrid management, and the importance of long-term follow-up for detecting delayed iatrogenic complications associated with endovascular procedures.
我们报告了一例62岁女性患者,她有长期难以控制的动脉高血压病史,尽管使用雷米普利治疗,但家庭血压平均读数约为140 - 160/100 - 110 mmHg,因左下肢急性严重缺血而紧急入院。影像学检查显示广泛的斯坦福B型主动脉夹层(TBAD),累及胸腹主动脉和髂动脉,左腿灌注明显受损。由于肢体缺血严重且立即进行血管内修复存在局限性,遂紧急进行了右向左股-股旁路手术以挽救肢体。术后,患者出现多器官并发症,包括需要血液透析的急性肾损伤(AKI)和肠缺血,均采取保守治疗。通过胸主动脉腔内修复术(TEVAR)完成了夹层的确定性修复。几周后,患者右肘前窝出现一个逐渐增大、无痛、搏动性肿块,对应于先前的动脉穿刺部位。临床特征,包括可触及的震颤和可闻及的杂音,与医源性动静脉瘘(AVF)相符,遂通过手术切除,同时保留动脉血流,患者恢复顺利。该病例强调了伴有外周灌注不良的复杂B型主动脉夹层的复杂且危及生命的病程、分期混合治疗的必要性以及长期随访对于检测与血管内手术相关的延迟医源性并发症的重要性。