纳米炭淋巴结示踪剂在cN0舌鳞状细胞癌颈淋巴清扫术中的应用
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  • 英文篇名:Application of carbon nanoparticles as lymph node tracers in patients with c N0 lingual squamous cell carcinoma undergoing neck dissection
  • 作者:李婷婷 ; 蒋灿华 ; 陈洁 ; 吴立萌 ; 张瑞璞 ; 翦新春
  • 英文作者:Li Tingting;Jiang Canhua;Chen Jie;Wu Limeng;Zhang Ruipu;Jian Xinchun;Dept.of Oral and Maxillofacial Surgery,Xiangya Hospital,Central South University;
  • 关键词:舌鳞状细胞癌 ; 颈淋巴清扫术 ; 纳米炭 ; 淋巴结示踪剂
  • 英文关键词:lingual squamous cell carcinoma;;neck dissection;;carbon nanoparticles;;lymph node tracers
  • 中文刊名:HXKQ
  • 英文刊名:West China Journal of Stomatology
  • 机构:中南大学湘雅医院口腔颌面外科;
  • 出版日期:2016-08-01
  • 出版单位:华西口腔医学杂志
  • 年:2016
  • 期:v.34
  • 基金:国家自然科学基金(81271154);; 中南大学临床科研基金(2015102)~~
  • 语种:中文;
  • 页:HXKQ201604024
  • 页数:6
  • CN:04
  • ISSN:51-1169/R
  • 分类号:85-90
摘要
目的探讨纳米炭淋巴结示踪剂在c N0舌鳞状细胞癌患者颈淋巴清扫术中的应用价值。方法选取96例c N0舌鳞状细胞癌患者作为研究对象,随机分为纳米炭组(试验组,50例)和对照组(46例),其中纳米炭组患者于术前12 h在距离肿块边缘0.5 cm处黏膜下多点注射纳米炭混悬注射液(每个注射点0.1 m L,共计3~4个注射点)。根据原发肿瘤的大小及部位选择行肩胛舌骨肌上(Ⅰ~Ⅲ区)或全颈(Ⅰ~Ⅴ区)淋巴清扫术。标本离体后解剖、分离所有淋巴结,并行病理学检查,记录检获的淋巴结数目、大小、部位、病理结果。将试验组与对照组所得数据进行比较,采用SPSS 19.0统计软件包进行统计学分析。结果 31例患者行肩胛舌骨肌上颈淋巴清扫术,共检出淋巴结1 137枚,纳米炭组平均每例检出淋巴结数(43.79±19.23)枚,显著高于对照组的(30.82±8.77)枚(P=0.019),两组均以Ⅲ区检出的淋巴结数最多,但纳米炭组Ⅱ区检出的淋巴结数及构成比均显著高于对照组(P=0.000)。65例全颈淋巴清扫术共检出淋巴结3 938枚,纳米炭组平均每例检出淋巴结数为(66.67±20.02)枚,对照组为(53.03±20.98)枚,两组差异有统计学意义(P=0.026),两组在各区(Ⅰ~Ⅴ区)检出淋巴结数的构成比的差异无统计学意义(P=0.354)。两种颈淋巴清扫术式中,纳米炭组检出微小淋巴结的比例和检获淋巴结的准确率均高于对照组(P=0.000);纳米炭组中染色淋巴结癌转移的检出率高于未染色的淋巴结(P=0.000)。结论纳米炭淋巴结示踪剂可以显著提高c N0舌鳞状细胞癌患者颈淋巴清扫术中淋巴结特别是微小淋巴结的检出率,有助于提高颈淋巴清扫术的彻底性和患者临床病理分期的准确性。
        Objective This study aimed to investigate the value of carbon nanoparticles as lymph node tracers in neck dissection for c N0 lingual squamous cell carcinoma patients. Methods Ninety-six patients with c N0 lingual squamous cell carcinoma were recruited to undergo surgical treatment were randomly divided into two groups, namely, the carbon nanoparticlelabeled group(the experimental group, 50 cases) and the control group(46 cases). Carbon nanoparticle suspension was injected into the submucosal layer around the site of the primary tumor at three or four points(0.1 m L for each point) 12 h before surgery. Supraomohyoid neck dissection(SOHND, Levels Ⅰ to Ⅲ) or comprehensive neck dissection(CND, Levels Ⅰto Ⅴ) were performed based on the size and location of the primary tumor. All the lymph nodes were dissected and separated from the ex vivo surgical specimens for histopathological evaluation. The number, size, location, and pathological result of all the lymph nodes were compared between the two groups. Statistical analyses were conducted by SPSS 19.0 software. Results A total of 1 137 lymph nodes were detected in 31 SOHND patients. The average number of lymph nodes detected in the experimental group was(43.79±19.23) /case, which was significantly higher than that in the control group [(30.82±8.77) /case](P=0.019). Level Ⅲ covered the largest number of lymph nodes in the two groups. However, the number and proportion of lymph nodes found in Level Ⅱ of the experimental group were significantly higher than those of the control group(P=0.000). A total of 3 938 lymph nodes were detected in 65 CND patients. The average number of lymph nodes detected in the experimental group [(66.67±20.02) /case] was larger than that in the control group [(53.03±20.98) /case](P=0.026). The difference in the lymph node location between the two groups was not statistically significant(P=0.354). In the two neck dissection methods, both the proportion of minute lymph nodes and the accuracy of the detected lymph nodes in the experimental group were significantly larger than those in the control groups(P=0.000). Compared with the control group, more metastases were proven by the carbon nanoparticlelabeled lymph nodes(P=0.000) in the experimental group. Conclusion Carbon nanoparticles as lymph node tracers in patients with c N0 lingual squamous cell carcinoma undergoing neck dissection can increase the number of detected lymph nodes, especially the minute nodes. Such nanoparticles can further ensure the thoroughness of neck dissection and the accuracy of clinicopathological stage.
引文
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