[早期结直肠癌前哨淋巴结的淋巴显像定位:单中心研究的结果和多中心方案的建议]。

S Sandrucci, B Mussa, M Goss, A Repici, M Bellò, G Bisi, A Mussa
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引用次数: 0

摘要

在结直肠癌中,前哨淋巴结清扫可能有助于识别原发肿瘤部位的任何异常肠系膜淋巴引流模式(前/跳过转移);假设准确的病理分期对治疗决策至关重要,我们正在进行一项研究,以评估前哨淋巴结技术在结直肠肿瘤中的可行性及其在预测区域淋巴结转移以适当分期方面的总体准确性。从2001年2月到2004年9月,我们纳入了30例直肠病变或变性结肠息肉未经内镜彻底切除的患者。在结肠或直肠病变的情况下,在手术前下午,用低分子量白蛋白胶体标记500Mci / 99mTc,体积为2ml,通过内镜途径在肿瘤周围的四个基本点进行粘膜下注射。闪烁图像是用装有通用准直器的伽马照相机获得的。干预当天,使用手持式伽马探测探头(scitiprobe m100, pol - tech, Italy)在体内和离体检测“热”节点。这些淋巴结在体内用针标记;标准切除标本,离体解剖SLN,单独送病理检查。在直肠病变的情况下,前哨淋巴结在体外搜索到直肠肠系膜脂肪。所有淋巴结,包括蓝淋巴结和热淋巴结,分别包埋,制作石蜡切片,进行苏木精和伊红染色。前哨淋巴结被提交多序列切片,以寻找微转移。使用放射性示踪剂,30例患者中有27例成功地确定了前哨淋巴结。27例中有23例(85%)观察到sln与淋巴结状态的一致性;2例(7.4%)患者被抢了风头,因为SLN是唯一的转移部位。在另外两个病例中,我们观察到阴性前哨淋巴结和非前哨淋巴结之间没有一致性(假阴性率,7.4%)。从这一经验出发,我们提出了一项关于前哨淋巴结技术在直肠癌和早期结直肠癌筛查中的价值的多中心试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Lymphoscintigraphic localization of sentinel lymph nodes in colorectal carcinoma in early stage: results of a single center study and proposal of a multicenter protocol].

In colorectal cancer the sentinel node dissection may help to identify any unusual mesenteric lymphatic drainage pattern from the primary tumor site (ex/skip metastases); assuming that accurate pathological staging is critical for therapeutic decisions we are conducing a study to evaluate the feasibility of the sentinel node technique in colorectal neoplasms and its overall accuracy in predicting regional lymph nodes metastases for appropriate staging. From February 2001 to September 2004 we included in this study 30 patients with rectal lesions or degenerate colonic polyps not radically excised by endoscopy. Lymphatic mapping was performed with low molecular weight albumin colloid labelled with 500Mci of 99mTc in a 2 ml volume and injected submucosally by an endoscopic route at the four cardinal points around the tumor, the afternoon before the surgical procedure, both in case of colonic or rectal lesions. Scintigraphic images were obtained with a gamma camera fitted with a general purpose collimator. The day of the intervention, a hand held gamma detecting probe (Scintiprobe m100, Pol-Hi-Tech, Italy) was employed to detect the "hot" nodes, in vivo and ex vivo. These lymph nodes were tagged with a stitch in vivo; the specimen was removed by a standard resection and SLN were dissected ex vivo and sent separately for pathological examination. In case of rectal lesions, the sentinel nodes were searched ex vivo into mesorectal fat in case. All lymph nodes, including blue or hot ones, were embedded separately for preparation of paraffin sections and haematoxylin and eosin staining. Sentinel lymph node were submitted to multi-seriate sections in order to look for micrometastases. Using the radioactive tracer, sentinel lymph nodes were successfully identified in 27 out of 30 patients. Concordance between SLNs and nodal status was observed in 23 out of 27 cases (85%); two patients (7.4%) were upstaged, as SLN was the only site of metastases. In another two cases we observed no concordance between negative sentinel node and non sentinel nodes (false negative rate, 7.4%). Starting from this experience we are proposing a multicentric trial concerning the value of sentinel node technique in rectal cancer and in early colorectal cancers detected by screening programs.

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