目的:观察胃癌组织淋巴管结构和分布特点,探讨微淋巴管密度(LMVD)与肿瘤淋巴转移的相关性。材料和方法:临床各期胃癌患者,施行胃癌切除术获得胃癌癌周组织和正常区胃组织标本切片,VEGFR-3抗体免疫组化染色,标记淋巴管,计数组织中LMVD。依据临床病理特征分析LMVD变化。结果:胃癌癌周组织与正常区组织石蜡切片各56例,在癌周区处于开放状态的功能性微淋巴管增多。胃癌癌周组织LM-VD(22.10±6.99个/HP×200)较远离癌肿区正常胃组织LMVD(10.63±1.90个/HP×200)增多(P=0.000)。胃癌癌周LMVD与淋巴转移、肿瘤大小和分期有关(P〈0.05),与分型和是否侵及浆膜无关(P〉0.05)。结论:胃癌癌周LMVD与肿瘤大小、分期和淋巴转移有密切关系,可以作为肿瘤诱导生成淋巴管研究的量化指标,有助于胃癌的预后判断及治疗方案的评价。
Objective: To investigate the relationship between lymphatic microvessel density (LMVD) and clinical pathology of gastric emeinoma. Methods: The expression of VEGFR - 3 in 56 gastric cancers (GC) was detected by inununohistoehemistry (SABC), by which the LMVD was calculated. Results: The lymphangiogenesis was shown in peritumoral tissue in GCs. The LMVD of peritumoral tissue in GCs (22.10 ±6.99) was significantly higher than that of normal gastric tissue ( 10.63 ± 1.90) ( P = 0.000). LMVD with lymphatic metastasis (25.43 ± 6.33) was higher than that without lymphatic metastasis ( 16.10 ± 2.93) (P=0,000). LMVDinpTNM Ⅲ +Ⅳ (24.88±6.71) was higher than that in pTNM Ⅰ + Ⅱ (16.22±2,50) (P=0.000). LMVD with big tumor lymphatic metastasis (25.43 ± 6.33) was higher than those without lymphatic metastasis ( 16.10 ± 2.93) (P=0.000), LMVDin pTNM Ⅲ +Ⅳ (24.88±6.71) was higher than that in pTNM Ⅰ + Ⅱ(16.22±2.50) (P= 0.000), LMVD with big tumor (diarneter≥5cm) (27.18 ± 6.95) was higher than those with small tumor (diameter〈 5cm) ( 19.28 ± 5,33) ( P = 0.002). There was no significant difference between LMVD and the tumor size and histopathologie type of cancer. (P 〉 0.05). Conclusion: LMVD in GCs showed oositive relations with pTNM stage and lymphatie metastasis.