Mathew G, Watson D I, Ellis T, De Young N, Rofe A M, Jamieson G G
The Royal Adelaide Centre for Endoscopic Surgery, Department of Surgery, Royal Adelaide Hospital, Adelaide, South Australia, 5000, Australia.
Surg Endosc. 1997 Dec;11(12):1163-6. doi: 10.1007/s004649900561.
A variety of mechanisms have been proposed to explain tumor growth in port sites following laparoscopic cancer surgery. We devised two experimental models to determine whether carbon dioxide (CO2) insufflation during laparoscopic surgery influences the movement of tumor cells and leads to tumor implantation and growth in surgical wounds.
Model 1: Viable adenocarcinoma cells were introduced into the upper abdomen of six syngeneic immune-competent rats during laparoscopy with CO2 insufflation; the same procedure was followed for a further six rats during gasless laparoscopy. A length of plastic tubing introduced through the anterolateral aspect of the rats' left lower abdominal wall was used to vent the insufflation gas through the abdomen of a recipient rat for 30 min. After 21 days, the peritoneal cavity and surgical wounds of the recipient rat were examined for implanted tumor. Model 2: A suspension of radiolabeled adenocarcinoma cells was introduced into the upper abdomen of five rats during laparoscopy with CO2 insufflation and an additional five rats during gasless laparoscopy. A length of plastic tubing introduced through the anterolateral aspect of the left lower abdominal flank was used to vent the insufflation gas through phosphate-buffered saline solution. After 30 min, the solution was counted for radioactivity.
Tumor growth occurred at the site of both the insufflation and venting ports in the second rat in five of the six rats from the group undergoing insufflation, but it was found in none of the gasless laparoscopy group (p = 0.015). In the second model, significant transfer of tumor cells to the vented gas occurred only in the rats undergoing laparoscopy with insufflation (median, 2.71% versus 0% of the introduced labeled cells; p = 0.008).
Carbon dioxide insufflation results in tumor dissemination during laparoscopy, leading to port site metastasis. Gasless laparoscopy may prevent this problem.
已经提出了多种机制来解释腹腔镜癌症手术后端口部位的肿瘤生长。我们设计了两个实验模型,以确定腹腔镜手术期间二氧化碳(CO₂)气腹是否会影响肿瘤细胞的移动,并导致肿瘤在手术伤口处种植和生长。
模型1:在有CO₂气腹的腹腔镜检查期间,将活的腺癌细胞引入6只同基因免疫活性大鼠的上腹部;另外6只大鼠在无气腹腔镜检查期间采用相同的程序。通过大鼠左下腹壁前外侧引入一段塑料管,用于通过受体大鼠的腹部排出气腹气体30分钟。21天后,检查受体大鼠的腹腔和手术伤口是否有植入的肿瘤。模型2:在有CO₂气腹的腹腔镜检查期间,将放射性标记的腺癌细胞悬液引入5只大鼠的上腹部,另外5只大鼠在无气腹腔镜检查期间引入。通过左下腹侧前外侧引入一段塑料管,用于通过磷酸盐缓冲盐溶液排出气腹气体。30分钟后,对溶液进行放射性计数。
在接受气腹的组中,6只大鼠中有5只的第二只大鼠的气腹和排气端口部位出现了肿瘤生长,但在无气腹腔镜检查组中均未发现(p = 0.015)。在第二个模型中,仅在接受气腹腹腔镜检查的大鼠中发生了肿瘤细胞向排出气体的显著转移(中位数,引入的标记细胞的2.71%对0%;p = 0.008)。
二氧化碳气腹导致腹腔镜检查期间肿瘤播散,导致端口部位转移。无气腹腔镜检查可能会预防这个问题。