Espey John, Acosta Stephen, Kolarczyk Lavinia, Long Jason
Department of Cardiothoracic Surgery, University of North Carolina-Chapel Hill, 101 Manning Drive, Chapel Hill, NC, 27705, USA.
Department of Anesthesiology, University of North Carolina-Chapel Hill, 101 Manning Drive, Chapel Hill, NC, 27705, USA.
J Cardiothorac Surg. 2020 Mar 30;15(1):54. doi: 10.1186/s13019-020-01093-3.
The first reported case of cardiac herniation was in 1948 and occurred following pericardiectomy during a lung cancer resection. Although rare, this potentially fatal surgical complication may occur following any operation in which a pericardial incision or resection is performed. The majority of literature on cardiac herniation involves case reports after intrapericardial pneumonectomy. Currently, there are no reports of cardiac herniation after thymectomy with pericardial resection.
A 44-year-old Asian female with symptomatic myasthenia gravis was referred for thymectomy. Originally thought to have Bell's Palsy, her symptoms began with right eyelid drooping and facial weakness. Over time, she developed difficulty holding her head up, upper extremity weakness, difficulty chewing and dysarthria. These symptoms worsened with activity. She was found to have positive acetylcholine receptor binding antibody on her myasthenia gravis panel. A preoperative CT scan demonstrated a 3.5 cm × 2 cm anterior mediastinal mass along the right heart border and phrenic nerve. A complete thymectomy, via right-sided robotic-assisted approach was performed en bloc with a portion of the right phrenic nerve and a 4 cm × 4 cm portion of pericardium overlying the right atrium and superior right ventricle. Upon undocking of the robot and closure of the port sites, the patient became acutely hypotensive (lowest recorded blood pressure 43/31 mmHg). The camera was reinserted and demonstrated partial cardiac herniation through the anterior pericardial defect toward the right chest. An emergent midline sternotomy was performed and the heart was manually reduced. The patient's hemodynamics stabilized. A vented Gore-Tex 6 cm × 6 cm patch was sewn along the pericardial edges with interrupted 4-0 prolene to close the pericardial defect.
This potentially fatal complication, although rare, should always be considered whenever there is hemodynamic instability entry or resection of the pericardium during surgery. We now routinely sew in a pericardial patch using our robotic surgical system for any defect over 3 cm × 3 cm that extends from the mid- to inferior portions of the heart.
首例心脏疝的报告病例于1948年出现,发生在肺癌切除术中的心包切除术后。尽管这种潜在致命的手术并发症很罕见,但在任何进行心包切开或切除的手术之后都可能发生。关于心脏疝的大多数文献都涉及心包内肺切除术后的病例报告。目前,尚无胸腺切除并心包切除术后发生心脏疝的报告。
一名44岁有症状的重症肌无力亚洲女性被转诊进行胸腺切除术。她最初被认为患有贝尔氏面瘫,症状始于右眼睑下垂和面部无力。随着时间的推移,她出现抬头困难、上肢无力、咀嚼困难和构音障碍。这些症状在活动时会加重。在她的重症肌无力检查中发现乙酰胆碱受体结合抗体呈阳性。术前CT扫描显示沿右心缘和膈神经有一个3.5厘米×2厘米的前纵隔肿块。通过右侧机器人辅助入路进行了完整的胸腺切除术,整块切除了部分右膈神经以及覆盖右心房和右心室上部的4厘米×4厘米的心包部分。在机器人撤离和关闭切口部位后,患者突然出现低血压(记录到的最低血压为43/31毫米汞柱)。重新插入摄像头后发现心脏通过心包前部缺损部分疝入右胸。紧急进行了正中胸骨切开术,并手动将心脏复位。患者的血流动力学稳定。用4-0聚丙烯缝线沿心包边缘间断缝合一块6厘米×6厘米的带孔戈尔特斯补片以封闭心包缺损。
这种潜在致命的并发症虽然罕见,但在手术中有血流动力学不稳定、进入或切除心包的任何情况下都应始终予以考虑。现在,对于任何从心脏中部至下部延伸且超过3厘米×3厘米的缺损,我们在使用机器人手术系统时会常规缝合心包补片。