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气腹后穿刺孔转移的发生

Development of port-site metastasis after pneumoperitoneum.

作者信息

Hirabayashi Y, Yamaguchi K, Shiraishi N, Adachi Y, Kitamura H, Kitano S

机构信息

Department of Surgery I, Oita Medical University, 1-1 Idaigaoka, Hasama-machi, Oita 879-5593, Japan.

出版信息

Surg Endosc. 2002 May;16(5):864-8. doi: 10.1007/s00464-001-9121-7. Epub 2002 Feb 8.

DOI:10.1007/s00464-001-9121-7
PMID:11997839
Abstract

BACKGROUND

Port-site metastasis is a critical problem in laparoscopic cancer surgery; the pathogenesis and means of prevention are still unclear. The aim of this study was to clarify by scanning electron microscopy the initial morphologic changes in the development of port-site metastasis.

METHODS

Fifteen nude mice were injected with human gastric cancer (MKN 45) cells. Mice were killed on days 0, 3, and 8 (n = 5 each day) after intraperitoneal injection of 5 x 105 cancer cells and carbon dioxide (CO2) pneumoperitoneum at 4-6 mmHg for 20 min. The abdominal wall with the port sites was harvested and examined under both light and scanning electron microscopy.

RESULTS

Immediately after CO2 pneumoperitoneum (day 0), the abdominal peritoneum was peeled away and the muscular layer was destroyed at the port site in all mice. Several cancer cells were attached to the injured port sites. On day 3, the subperitoneal tissue and muscular layer defects were replaced by granulation tissue, and several cancer cells were observed in the subperitoneal tissue. On day 8, a small nodule was macroscopically visible at the port site; it was completely covered by mesothelial cells and consisted of numerous cancer cells.

CONCLUSIONS

Free cancer cells appear to attach to the injured port sites immediately after CO2 pneumoperitoneum, and these are associated with the development of port-site metastasis after laparoscopic cancer surgery.

摘要

背景

端口部位转移是腹腔镜癌症手术中的一个关键问题;其发病机制和预防方法仍不清楚。本研究的目的是通过扫描电子显微镜阐明端口部位转移发展过程中的初始形态学变化。

方法

将15只裸鼠注射人胃癌(MKN 45)细胞。在腹腔注射5×10⁵个癌细胞并在4 - 6 mmHg下进行20分钟二氧化碳(CO₂)气腹后,于第0天、第3天和第8天处死小鼠(每天n = 5)。采集带有端口部位的腹壁,在光学显微镜和扫描电子显微镜下进行检查。

结果

在二氧化碳气腹后立即(第0天),所有小鼠端口部位的腹膜被剥离,肌肉层被破坏。有几个癌细胞附着在受损的端口部位。在第3天,腹膜下组织和肌肉层缺损被肉芽组织替代,在腹膜下组织中观察到几个癌细胞。在第8天,端口部位肉眼可见一个小结节;它完全被间皮细胞覆盖,由大量癌细胞组成。

结论

游离癌细胞似乎在二氧化碳气腹后立即附着在受损的端口部位,并且这些与腹腔镜癌症手术后端口部位转移的发生有关。

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本文引用的文献

1
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Surg Endosc. 2001 Sep;15(9):954-8. doi: 10.1007/s004640090100. Epub 2001 Jun 12.
2
Enhancement of port site metastasis by hyaluronic acid under CO2 pneumoperitoneum in a murine model.在小鼠模型中,二氧化碳气腹下透明质酸对端口部位转移的促进作用。
Surg Endosc. 2001 May;15(5):504-7. doi: 10.1007/s004640090016. Epub 2001 Feb 6.
3
Convenient murine pneumoperitoneal model for the study of laparoscopic cancer surgery.
日本一项关于结直肠癌腹腔镜手术的多中心研究。
Surg Endosc. 2006 Sep;20(9):1348-52. doi: 10.1007/s00464-004-8247-9. Epub 2006 Jul 24.
4
Influence of CO2 pneumoperitoneum on intracellular pH and signal transduction in cancer cells.二氧化碳气腹对癌细胞内pH值及信号转导的影响。
J Zhejiang Univ Sci B. 2005 Jul;6(7):650-5. doi: 10.1631/jzus.2005.B0650.
5
Increased peritoneal dissemination after laparotomy versus pneumoperitoneum in a mouse cecal cancer model.在小鼠盲肠癌模型中,剖腹手术与气腹手术后腹膜播散增加。
Surg Endosc. 2004 Dec;18(12):1795-9. doi: 10.1007/s00464-003-9322-3. Epub 2004 Oct 26.
6
Port-site metastasis after CO2 pneumoperitoneum: role of adhesion molecules and prevention with antiadhesion molecules.
Surg Endosc. 2004 Jul;18(7):1113-7. doi: 10.1007/s00464-003-9150-5. Epub 2004 May 12.
7
The effects of staging laparoscopy on trocar site and peritoneal recurrence of pancreatic cancer.分期腹腔镜检查对胰腺癌套管针穿刺部位及腹膜复发的影响。
Surg Endosc. 2004 Feb;18(2):310-3. doi: 10.1007/s00464-003-8909-z. Epub 2003 Dec 29.
Surg Laparosc Endosc Percutan Tech. 1999 Aug;9(4):279-81.
4
Intraperitoneal immunity and pneumoperitoneum.腹腔内免疫与气腹
Surg Endosc. 1999 Nov;13(11):1135-8. doi: 10.1007/s004649901189.
5
The influence of pneumoperitoneum used in laparoscopic surgery on an intraabdominal tumor growth.
Cancer. 1999 Sep 1;86(5):770-4.
6
Characteristic alterations of the peritoneum after carbon dioxide pneumoperitoneum.二氧化碳气腹后腹膜的特征性改变。
Surg Endosc. 1999 Jun;13(6):611-4. doi: 10.1007/s004649901052.
7
A model of port-site metastases of gallbladder cancer: the influence of peritoneal injury and its repair on abdominal wall metastases.胆囊癌腹壁转移模型:腹膜损伤及其修复对腹壁转移的影响。
Surgery. 1999 May;125(5):553-9.
8
Peritoneal irrigation with povidone-iodine solution after laparoscopic-assisted splenectomy significantly decreases port-tumor recurrence in a murine model.在小鼠模型中,腹腔镜辅助脾切除术后用聚维酮碘溶液进行腹腔灌洗可显著降低端口肿瘤复发率。
Dis Colon Rectum. 1999 Mar;42(3):319-26. doi: 10.1007/BF02236346.
9
Influence of cytotoxic agents on intraperitoneal tumor implantation after laparoscopy.细胞毒性药物对腹腔镜检查后腹腔内肿瘤种植的影响。
Dis Colon Rectum. 1999 Jan;42(1):10-5. doi: 10.1007/BF02235176.
10
Experimental study of the effect of intraperitoneal heparin on tumour implantation following laparoscopy.腹腔镜术后腹腔内注射肝素对肿瘤种植影响的实验研究
Br J Surg. 1999 Mar;86(3):400-4. doi: 10.1046/j.1365-2168.1999.01031.x.