Wilkinson N W, Shapiro A J, Harvey S B, Stack R S, Cornum R L
Department of Surgery, Eisenhower Army Medical Center, Fort Gordon, GA 30905, USA.
JSLS. 2001 Jul-Sep;5(3):221-6.
The use of advanced laparoscopy remains controversial in the field of surgical oncology because the potential for port-site recurrence may violate sound oncologic principles. Two mechanisms are theorized to be the cause of port-site recurrences: first, indirect contamination caused by pneumoperitoneum, aerosolization, or intraperitoneal spread, and second, direct contamination by physical trocar seeding.
A VX-2 carcinoma cell suspension was transferred under the left renal capsule of 31 rabbits with either an open flank incision (16) or laparoscopy (15). Animals were observed for tumor recurrence at the video port, the working port, and the open incision. Intraoperative findings and necropsy were used to document recurrence.
The open incision technique resulted in local tumor recurrence in 1/16 animals with 16/16 viable intraabdominal tumors. The laparoscopic technique resulted in 0/15 video port-site recurrences and 9/15 working port-site recurrences, with 14/15 viable intraabdominal tumors. Recurrence at the laparoscopic working port occurred more frequently than in the open (P < 0.02) or laparoscopic video port groups (P < 0.007). No significant difference existed in recurrence between the open incision and the laparoscopic video port (P > 0.5).
Laparoscopic port-site recurrences can be reproduced using the transplantable VX-2 rabbit carcinoma model. In the VX-2 model, trocar recurrence is the result of direct contamination via surgical instrumentation of viable tumor cells. The effect of the pneumoperitoneum or intraperitoneal cytological spillage (indirect contamination) does not have any effect on trocar recurrence. This model can be used to test and improve laparoscopic techniques to minimize the risk of port-site recurrence. Until technological advances have eliminated the risk of trocar recurrences, direct contact between malignant cells and laparoscopic instruments should be performed with caution.
在外科肿瘤学领域,先进腹腔镜技术的应用仍存在争议,因为端口部位复发的可能性可能违反合理的肿瘤学原则。理论上认为端口部位复发有两种机制:第一,由气腹、雾化或腹腔内播散引起的间接污染;第二,套管针直接植入导致的直接污染。
将VX - 2癌细胞悬液通过开放侧腹切口(16只)或腹腔镜手术(15只)植入31只兔子的左肾包膜下。观察动物在视频端口、操作端口和开放切口处的肿瘤复发情况。术中发现和尸检用于记录复发情况。
开放切口技术导致1/16的动物出现局部肿瘤复发,腹腔内有16/16个存活肿瘤。腹腔镜技术导致视频端口部位复发率为0/15,操作端口部位复发率为9/15,腹腔内有14/15个存活肿瘤。腹腔镜操作端口的复发比开放组(P < 0.02)或腹腔镜视频端口组(P < 0.007)更频繁。开放切口和腹腔镜视频端口之间的复发无显著差异(P > 0.5)。
使用可移植的VX - 2兔癌模型可重现腹腔镜端口部位复发。在VX - 2模型中,套管针复发是活肿瘤细胞通过手术器械直接污染的结果。气腹或腹腔细胞学溢出(间接污染)对套管针复发没有任何影响。该模型可用于测试和改进腹腔镜技术,以尽量减少端口部位复发的风险。在技术进步消除套管针复发风险之前,应谨慎进行恶性细胞与腹腔镜器械的直接接触。