微淋巴管密度对直肠癌手术远端切除长度的临床意义

目的研究低位直肠癌的微淋巴管密度（LVD）与直肠癌远端扩散（DIS）长度的关系，探讨LVD在低位直肠癌手术时对决定远端切除长度的价值。方法92例低位直肠癌手术标本通过苏木精．伊红染色测定DIS，利用淋巴管内皮细胞透明质酸受体（LYVE-1）免疫组织化学法测定LVD，分析LVD与DIS及直肠癌其他临床病理学因素间的关系。结果44例（47．8％）患者有DIS，为（0．31±0．09）cm；其中有23例（52．3％）淋巴管内癌栓。癌缘LVD明显高于癌内，DIS组明显高于无DIS组。相关分析显示，DIS组中，癌缘LVD与DIS呈正相关（r=0．755，P〈0．01）；当癌缘LVD超过38时，DIS均超过1cm。LVD还与浸润程度、淋巴结转移和淋巴浸润有关。结论淋巴管内癌栓是直肠癌DIS的主要形式．LVD与DIS的相关关系有助于决定低位直肠癌手术中的远端切除长度。     

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低位直肠癌是指肿瘤下缘距肛缘 7cm以下或位于直肠下 1 /3段的直肠癌。随着对直肠癌转移规律的认识和吻合技术、吻合器械等的发展,保留肛门括约肌的根治术 (简称保肛根治术 )在低位直肠癌的手术中所占比例已高达80%,成为主流术式。1　低位直肠癌保肛根治术的理论基础对低位直肠癌来说,癌肿远侧肠管切除的安全距离是决定能否保肛的主要因素。近 30年的研究表明,直肠癌通过直接浸润、淋巴管癌栓、小静脉癌栓等途径向远侧肠壁内浸润的发生率为 8% ~24%,浸润范围绝大多数在 1cm以内, 1~2cm者仅 2 7% ~5%,超过 2cm者 0~2 5%。临床资料显示切…     

大切片CK20染色对中下段直肠癌远端转移的研究

目的 探讨中下段直肠癌远端壁内浸润和系膜转移的频率、类型,确定合适的病灶远端切除长度.方法 收集中山大学肿瘤医院2004年8月至2005年12月中下段直肠癌标本34例,山东省立医院2006年10月至2007年10月中下段直肠癌标本28例,分别用HE和CK20(cytokeratin,CK)染色,观察中下段直肠癌远端癌灶存在形式及分布规律.Logistic回归分析筛选与中下段直肠癌发生远端壁内浸润和系膜转移的临床病理因素.结果 直肠癌远端肠壁浸润形式为:黏膜下或肌肉间浸润发生率为16%(10/62),扩散距离0.5～1.0 cm.直肠癌远端系膜转移形式为:淋巴结转移、脉管转移、周围神经转移、孤立癌灶,发生率为24%(15/62),扩散距离0.5～4.0 cm.CK20染色观察3例患者存在远端系膜癌灶.Logistic单因素分析显示,血CEA水平、淋巴结转移、环周切缘癌浸润(circumferential margin involvement,CMI)和TNM分期与中下段直肠癌远端肠壁浸润和系膜转移有关.多因素分析显示,TNM分期是中下段直肠癌远端转移的独立影响因素(Wald=9.567,P=0.002).结论 TNM分期是影响中下段直肠癌远端壁内浸润和系膜转移的独立因素.直肠癌手术切除远端肠管长度达1.5 cm即可,但必须保证切除远端系膜长度不少于5 cm.     

直肠癌直肠系膜播散的临床病理观察

目的探讨直肠癌根治术直肠系膜的合理切除范围。方法采用连续病理切片方法观察40例直肠癌的手术标本。结果40例直肠癌中发现直肠系膜有癌播散6例(15%),播散方式有肿瘤直接浸润、在系膜中形成孤立癌灶、血管和(或)淋巴管的转移。播散范围均在肿瘤下缘4cm之内。直肠癌直肠系膜播散与肿瘤分型、分化程度、肠壁浸润深度相关,与肿瘤大小及癌胚抗原(CEA)水平无相关。结论直肠癌根治术中直肠系膜的远端切缘应超过肿瘤下缘4cm。     

中下段直肠癌远端壁内浸润和系膜转移的研究

目的 探讨中下段直肠癌远端壁内浸润和系膜转移的频率、类型,确定合适的远端切除长度.方法 对中山大学肿瘤医院2004年8月至2005年12月中下段直肠癌标本34例和山东省立医院2006年10月至2007年10月中下段直肠癌标本28例做病理学检查.用Logistic回归分析筛选与中下段直肠癌发生远端壁内浸润和系膜转移的临床病理因素.结果 直肠癌远端肠壁浸润形式为:黏膜下或肌肉间浸润,发生率为16%(10/62),浸润距离为0.5～1.0 cm.直肠癌远端系膜转移形式为:淋巴结转移、脉管转移、围神经转移、孤立癌灶,转移率为19%(12/62),浸润距离为0.5-4.0cm.Logistic单因素分析:血癌胚抗原(carcinoembryonic antigen,CEA)水平、淋巴结转移、环周切缘癌浸润和Dukes分期与中下段直肠癌远端肠壁浸润和系膜转移有关.多因素分析:Dukes分期是独立影响因素.结论 Dukes分期是影响中下段直肠癌远端壁内浸润和系膜转移的独立因素(Wald=8.386,P=0.004).直肠癌手术切除远端肠管的长度最少为1.5 cm,但必须保证切除远端系膜的长度＞5.0 cm.     

直肠癌大组织切片系膜九分区法病理学研究

目的　探索直肠癌全直肠系膜切除术 (TME)的必要性和选择性全直肠系膜切除术(STME)的最佳切除范围。方法　以 31例直肠癌TME手术标本为对象 ,纵向由远及近以 5mm的间距连续取材 ,常规固定包埋 ,大组织切片机以 2 .5cm的间隔连续切片 ,HE染色 ,光学显微镜观察结果。将直肠系膜等分为内、中、外三个带 ,每带按左、右、后三个方向分为三个区 ,直肠癌在直肠系膜内的转移灶分别定位于上述九个区。结果　直肠系膜外带内癌转移 1 4例 (4 5 .2 % ) ,全部为低位直肠癌 ;远端直肠系膜 (DMR)内癌转移 2例 (6 .5 % ) ,均在原发灶下缘以远 3.0cm以内 ;环周切缘癌浸润 2例 (6 .5 % )。结论　低位直肠癌根治手术时 ,完整地切除直肠系膜非常必要 ;远端直肠系膜的切除应达到肿瘤下缘以远 4cm。     

97例直肠癌微血管计数与远端扩散长度的关系研究

目的　探讨直肠癌微血管计数 (microvesselcount,MVC)和远端扩散长度的关系 ,为手术时确定直肠癌远端切除长度提供参考指标。方法　对 1997年 1月至 2 0 0 1年 11月直肠癌根治标本 97例 ,用Ⅷ因子相关抗原 (F8 RA)单克隆抗体SP免疫组化法测定其直肠癌组织的MVC ,并连续切片 ,在光镜下观测直肠癌的远端壁内扩散长度 ,再进行分析比较。结果　远端发生扩散的直肠癌4 7例 ,平均MVC为 2 8± 5 ,明显高于没有远端扩散的 5 0例的MVC (2 0± 5 ) ,且MVC较高的直肠癌远端扩散距离也较长。结论　直肠癌手术时远端一般切除 2～ 3cm即足够 ,但MVC较高的病例 ,远端扩散距离较长 ,手术远端切除长度也要延长。术前活检确诊直肠癌的同时测定MVC ,可作为决定远端切除长度的参考指标。     

早期胃癌淋巴结转移和临床病理特征的关系(附467例报道)

目的:探讨早期胃癌病人各临床病理因素与淋巴结转移的关系,为制定合理的治疗方案提供帮助.方法:对467例早期胃癌病人进行回顾性分析,对其年龄、性别、肿瘤大小、大体类型、分化程度、浸润深度、淋巴管癌栓与淋巴结转移的关系进行单因素和多因素分析.结果:影响早期胃癌淋巴结转移的因素主要有:肿瘤大小(最大径,≤2 cm比>2 cm,P<0.01)、分化程度(分化良好比分化不佳,P<0.01)、浸润深度(黏膜层比黏膜下层,P<0.01)、淋巴管癌栓(无比有,P<0.01).Logistic回归多因素分析结果显示,肿瘤大小、分化程度、浸润深度、淋巴管癌浸润均是提示胃癌是否有淋巴结转移的独立因素.结论:早期胃癌淋巴结转移与肿瘤大小、肿瘤分化程度、浸润深度、淋巴管癌栓等因素有关.确定早期胃癌手术方案时,可参考上述因素判断淋巴结转移风险,决定是否行淋巴结清扫术.     

直肠癌远端壁内扩散的病理分析

５０例直肠癌切除标本，远端壁内扩散为２１例，其中１９例扩散距离〈１ｃｍ。其与癌的大体类型、大小、组织类类型和分化程度、肠壁浸润深度、淋巴结转移不同程度的关系。据此，考虚标本固定的因素，对中低位直肠远端切除长度进行了探讨。     

直肠拖出肛门外切除术治疗超低位直肠肿瘤15例报告

传统的观点认为低位直肠癌需行Miles手术,随着低位直肠癌远端肠管切除2 cm安全距离的认识、全直肠系膜切除术和吻合器技术的应用,对于低位直肠癌,直肠低位前切除术已成为主流术式。而部分直肠肿瘤距肛缘4～6 cm或肥胖、盆腔狭窄,无法经腹手术完成远端直肠的关闭、切割及直肠、     

杭州健康女性定量骨超声测定原发性骨质疏松

目的 评价杭州健康女性骨超声速度(SOS)值随增龄减少和骨质疏松患病率，建立杭州地区女性骨超声速度值参考数据库。方法 定量超声法测定1208例杭州地区健康女性桡骨远端(RAD)，第3指骨近节(PLX)，第V跖骨(MTR)和胫骨中段(TIB)的超声速度值。结果 RAD、PLX、MTR和TIBSOS峰值(Peak of SOS)均出现在40-45岁，TJB的SOS峰值出现在35—40岁，此后随年龄增长而下降。绝经后妇女在绝经后早期和晚期各有1个SOS快速减少期，前见于桡骨近端，平均年减少率为2．4％，后见于胫骨中段，平均年减少率为1．8％。各部位骨SOS累积减少率随年龄增长而增加，到85岁4部位累积减少为13％-18％。60岁以后骨质疏松性症(OP)检出率为45％-70％，OP检出率以桡骨远端最高，60-70岁平均为67％，第3指骨近端次之约50％，胫骨中段最低为36％；75岁以后分别为70％，65％和45％。结论 全身各部位骨超声速度值到达峰值的年龄不同，峰值也各有差异。绝经后妇女骨超声速度值随年龄增加减少较快，应予激素和补钙治疗，桡骨远端为本地区SOS检测和OP检出的敏感部位。     

Importance of echocardiography in prognosis of surgical outcomes in cholecystitis in elderly patients

The authors propose to use more often echocardiography (EchoCG) in examination of elderly (over 60 years) of age patients with cholecystitis that permits to increase surgical activity to 92.4%. Left ventricular ejection fraction is the most informative. When this fraction is lower than 45% surgery must be recommended on vital indications only. EchoCG was used in 155 patients with cholecystitis, 131 of them were operated. 2 (1.52%) patients died due to acute cardio-vascular insufficiency and pulmonary artery thromboembolism.     

脊髓胶质细胞在小鼠骨癌痛形成中的作用

Objective To evaluate the role of gliocyte in the spinal cord in the development of bone cancer pain (BCP) in mice. Methods Forty male C3H/He mice aged 8-10 weeks weighing 18-22 g were randomly divided into 4 groups ( n = 10 each) : group I sham operation (group S) , group II BCP, group Ⅲ PBS and group IV minocyline (group M) . In group BCP, PBS and M, bone cancer pain was produced by injection of NCTC2472 fibrosarcoma cell suspension (2 x 105 cells) 10 μl into medullary cavity of calcaneus bone, while in group S, PBS solution 10 μl was injected instead of cancer cell suspension. In group PBS and M, PBS 5 μl and minocyline 5 μl (dissolved to 0.2 mmol/L in PBS)_were given IT immediately before cancer cell inoculation once a day for 11 consecutive days respectively. Mechanical pain threshold was measured at 1 d before cancer cell inoculation, and at 0, 3, 5, 7, 9 and 11d after cancer cell inoculation. Cold pain threshold was measured at 3, 7, 9 and 11d after cancer cell inoculation. The animals were killed after measurement of pain threshold and L4-6, segment of spinal cord was removed for determination of GFAP and CD11b expression by Western blot. Results Compared with group S, mechanical pain threshold was significantly increased at 3-11 d after cancer cell inoculation in group BCP and PBS, and at 3 and S d after cancer cell inoculation in group M, and cold pain threshold was significantly increased at 7-11 d after cancer cell inoculation, and expression of CD11b and GFAP was up-regulated in group BCP, PBS and M ( P < 0.05) . Compared with group BCP, mechanical pain threshold was significantly decreased at 3-11 d after cancer cell inoculation, cold pain threshold was significantly decreased at 7-11 d after cancer cell inoculation, and expression of CD11b and GFAP was down-regulated in group M ( P <0.05) . ConclusionThe activiton of gliocyte in the spinal cord is involved in the development of bone cancer pian in mice.     

脊髓胶质细胞在小鼠骨癌痛形成中的作用

Objective To evaluate the role of gliocyte in the spinal cord in the development of bone cancer pain (BCP) in mice. Methods Forty male C3H/He mice aged 8-10 weeks weighing 18-22 g were randomly divided into 4 groups ( n = 10 each) : group I sham operation (group S) , group II BCP, group Ⅲ PBS and group IV minocyline (group M) . In group BCP, PBS and M, bone cancer pain was produced by injection of NCTC2472 fibrosarcoma cell suspension (2 x 105 cells) 10 μl into medullary cavity of calcaneus bone, while in group S, PBS solution 10 μl was injected instead of cancer cell suspension. In group PBS and M, PBS 5 μl and minocyline 5 μl (dissolved to 0.2 mmol/L in PBS)_were given IT immediately before cancer cell inoculation once a day for 11 consecutive days respectively. Mechanical pain threshold was measured at 1 d before cancer cell inoculation, and at 0, 3, 5, 7, 9 and 11d after cancer cell inoculation. Cold pain threshold was measured at 3, 7, 9 and 11d after cancer cell inoculation. The animals were killed after measurement of pain threshold and L4-6, segment of spinal cord was removed for determination of GFAP and CD11b expression by Western blot. Results Compared with group S, mechanical pain threshold was significantly increased at 3-11 d after cancer cell inoculation in group BCP and PBS, and at 3 and S d after cancer cell inoculation in group M, and cold pain threshold was significantly increased at 7-11 d after cancer cell inoculation, and expression of CD11b and GFAP was up-regulated in group BCP, PBS and M ( P < 0.05) . Compared with group BCP, mechanical pain threshold was significantly decreased at 3-11 d after cancer cell inoculation, cold pain threshold was significantly decreased at 7-11 d after cancer cell inoculation, and expression of CD11b and GFAP was down-regulated in group M ( P <0.05) . ConclusionThe activiton of gliocyte in the spinal cord is involved in the development of bone cancer pian in mice.     

脊髓胶质细胞在小鼠骨癌痛形成中的作用

Objective To evaluate the role of gliocyte in the spinal cord in the development of bone cancer pain (BCP) in mice. Methods Forty male C3H/He mice aged 8-10 weeks weighing 18-22 g were randomly divided into 4 groups ( n = 10 each) : group I sham operation (group S) , group II BCP, group Ⅲ PBS and group IV minocyline (group M) . In group BCP, PBS and M, bone cancer pain was produced by injection of NCTC2472 fibrosarcoma cell suspension (2 x 105 cells) 10 μl into medullary cavity of calcaneus bone, while in group S, PBS solution 10 μl was injected instead of cancer cell suspension. In group PBS and M, PBS 5 μl and minocyline 5 μl (dissolved to 0.2 mmol/L in PBS)_were given IT immediately before cancer cell inoculation once a day for 11 consecutive days respectively. Mechanical pain threshold was measured at 1 d before cancer cell inoculation, and at 0, 3, 5, 7, 9 and 11d after cancer cell inoculation. Cold pain threshold was measured at 3, 7, 9 and 11d after cancer cell inoculation. The animals were killed after measurement of pain threshold and L4-6, segment of spinal cord was removed for determination of GFAP and CD11b expression by Western blot. Results Compared with group S, mechanical pain threshold was significantly increased at 3-11 d after cancer cell inoculation in group BCP and PBS, and at 3 and S d after cancer cell inoculation in group M, and cold pain threshold was significantly increased at 7-11 d after cancer cell inoculation, and expression of CD11b and GFAP was up-regulated in group BCP, PBS and M ( P < 0.05) . Compared with group BCP, mechanical pain threshold was significantly decreased at 3-11 d after cancer cell inoculation, cold pain threshold was significantly decreased at 7-11 d after cancer cell inoculation, and expression of CD11b and GFAP was down-regulated in group M ( P <0.05) . ConclusionThe activiton of gliocyte in the spinal cord is involved in the development of bone cancer pian in mice.     

脊髓胶质细胞在小鼠骨癌痛形成中的作用

Objective To evaluate the role of gliocyte in the spinal cord in the development of bone cancer pain (BCP) in mice. Methods Forty male C3H/He mice aged 8-10 weeks weighing 18-22 g were randomly divided into 4 groups ( n = 10 each) : group I sham operation (group S) , group II BCP, group Ⅲ PBS and group IV minocyline (group M) . In group BCP, PBS and M, bone cancer pain was produced by injection of NCTC2472 fibrosarcoma cell suspension (2 x 105 cells) 10 μl into medullary cavity of calcaneus bone, while in group S, PBS solution 10 μl was injected instead of cancer cell suspension. In group PBS and M, PBS 5 μl and minocyline 5 μl (dissolved to 0.2 mmol/L in PBS)_were given IT immediately before cancer cell inoculation once a day for 11 consecutive days respectively. Mechanical pain threshold was measured at 1 d before cancer cell inoculation, and at 0, 3, 5, 7, 9 and 11d after cancer cell inoculation. Cold pain threshold was measured at 3, 7, 9 and 11d after cancer cell inoculation. The animals were killed after measurement of pain threshold and L4-6, segment of spinal cord was removed for determination of GFAP and CD11b expression by Western blot. Results Compared with group S, mechanical pain threshold was significantly increased at 3-11 d after cancer cell inoculation in group BCP and PBS, and at 3 and S d after cancer cell inoculation in group M, and cold pain threshold was significantly increased at 7-11 d after cancer cell inoculation, and expression of CD11b and GFAP was up-regulated in group BCP, PBS and M ( P < 0.05) . Compared with group BCP, mechanical pain threshold was significantly decreased at 3-11 d after cancer cell inoculation, cold pain threshold was significantly decreased at 7-11 d after cancer cell inoculation, and expression of CD11b and GFAP was down-regulated in group M ( P <0.05) . ConclusionThe activiton of gliocyte in the spinal cord is involved in the development of bone cancer pian in mice.     

脊髓胶质细胞在小鼠骨癌痛形成中的作用

目的 评价脊髓胶质细胞在小鼠骨癌痛形成中的作用.方法 健康雄性C3H/He小鼠40只,周龄8～10周,体重18～22 g,随机分为4组(n=10):假手术组(S组)、骨癌痛组(B组)、PBS组(P组)和米诺环素组(M组).S组跟骨骨髓腔内注射PBS 10 μl;余3组跟骨骨髓腔内注射含2×105个骨纤维肉瘤细胞的PBS 10 μl制备骨癌痛模型,于造模前即刻开始PBS组鞘内注射PBS 5μl,M组鞘内注射米诺环素(用PBS溶解为0.2 mmol/L)5μl,1次/d,连续11 d.于造模前1 d、造模后即刻、3、5、7、9、11 d时测定机械痛阈;于造模后3、7、9、11 d机械痛阈测定结束后测定冷痛阈.痛阈测定结束后处死小鼠,取脊髓组织,测定神经胶质纤维酸性蛋白(GFAP)和CD11b的表达水平.结果 与S组比较,B组和P组造模后3-11 d时、M组造模后3、5 d时机械痛阈升高,B组、P组和M组造模后7～11 d时冷痛阈升高,脊髓CD11b和GFAP表达上调(P<0.05).与B组比较,M组造模后3-11 d时机械痛阈降低,造模后7-11 d时冷痛阈降低,脊髓CD11b和GFAP表达下调(P<0.05).结论 脊髓胶质细胞(星形胶质细胞和小胶质细胞)的激活参与了小鼠骨癌痛的形成.     

脊髓胶质细胞在小鼠骨癌痛形成中的作用

Objective To evaluate the role of gliocyte in the spinal cord in the development of bone cancer pain (BCP) in mice. Methods Forty male C3H/He mice aged 8-10 weeks weighing 18-22 g were randomly divided into 4 groups ( n = 10 each) : group I sham operation (group S) , group II BCP, group Ⅲ PBS and group IV minocyline (group M) . In group BCP, PBS and M, bone cancer pain was produced by injection of NCTC2472 fibrosarcoma cell suspension (2 x 105 cells) 10 μl into medullary cavity of calcaneus bone, while in group S, PBS solution 10 μl was injected instead of cancer cell suspension. In group PBS and M, PBS 5 μl and minocyline 5 μl (dissolved to 0.2 mmol/L in PBS)_were given IT immediately before cancer cell inoculation once a day for 11 consecutive days respectively. Mechanical pain threshold was measured at 1 d before cancer cell inoculation, and at 0, 3, 5, 7, 9 and 11d after cancer cell inoculation. Cold pain threshold was measured at 3, 7, 9 and 11d after cancer cell inoculation. The animals were killed after measurement of pain threshold and L4-6, segment of spinal cord was removed for determination of GFAP and CD11b expression by Western blot. Results Compared with group S, mechanical pain threshold was significantly increased at 3-11 d after cancer cell inoculation in group BCP and PBS, and at 3 and S d after cancer cell inoculation in group M, and cold pain threshold was significantly increased at 7-11 d after cancer cell inoculation, and expression of CD11b and GFAP was up-regulated in group BCP, PBS and M ( P < 0.05) . Compared with group BCP, mechanical pain threshold was significantly decreased at 3-11 d after cancer cell inoculation, cold pain threshold was significantly decreased at 7-11 d after cancer cell inoculation, and expression of CD11b and GFAP was down-regulated in group M ( P <0.05) . ConclusionThe activiton of gliocyte in the spinal cord is involved in the development of bone cancer pian in mice.     

脊髓胶质细胞在小鼠骨癌痛形成中的作用

Objective To evaluate the role of gliocyte in the spinal cord in the development of bone cancer pain (BCP) in mice. Methods Forty male C3H/He mice aged 8-10 weeks weighing 18-22 g were randomly divided into 4 groups ( n = 10 each) : group I sham operation (group S) , group II BCP, group Ⅲ PBS and group IV minocyline (group M) . In group BCP, PBS and M, bone cancer pain was produced by injection of NCTC2472 fibrosarcoma cell suspension (2 x 105 cells) 10 μl into medullary cavity of calcaneus bone, while in group S, PBS solution 10 μl was injected instead of cancer cell suspension. In group PBS and M, PBS 5 μl and minocyline 5 μl (dissolved to 0.2 mmol/L in PBS)_were given IT immediately before cancer cell inoculation once a day for 11 consecutive days respectively. Mechanical pain threshold was measured at 1 d before cancer cell inoculation, and at 0, 3, 5, 7, 9 and 11d after cancer cell inoculation. Cold pain threshold was measured at 3, 7, 9 and 11d after cancer cell inoculation. The animals were killed after measurement of pain threshold and L4-6, segment of spinal cord was removed for determination of GFAP and CD11b expression by Western blot. Results Compared with group S, mechanical pain threshold was significantly increased at 3-11 d after cancer cell inoculation in group BCP and PBS, and at 3 and S d after cancer cell inoculation in group M, and cold pain threshold was significantly increased at 7-11 d after cancer cell inoculation, and expression of CD11b and GFAP was up-regulated in group BCP, PBS and M ( P < 0.05) . Compared with group BCP, mechanical pain threshold was significantly decreased at 3-11 d after cancer cell inoculation, cold pain threshold was significantly decreased at 7-11 d after cancer cell inoculation, and expression of CD11b and GFAP was down-regulated in group M ( P <0.05) . ConclusionThe activiton of gliocyte in the spinal cord is involved in the development of bone cancer pian in mice.