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肾细胞肿瘤
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  renal cell tumors
     Conclusion Nephron sparing surgery or partial nephrectomy in seleced cases were indicated for T_1,T_2 renal cell tumors.
     结论 保肾手术或肾部分切除术适合于浸润黏膜固有层(T1)、浸润肌层(T2 )的肾细胞肿瘤
短句来源
     Results Of 229 renal cell tumors which comprised of 89.1%(229/257) of simultaneously removed renal parenchymal neoplasms,223 cases were classified renal cell carcinoma(RCC),6 cases were oncocytoma.
     结果229例肾细胞肿瘤占同期肾实质肿瘤89.1%(229/257),其中223例(97.4%)为肾细胞癌,6例(2.6%)为肾嗜酸细胞腺瘤。
短句来源
     Methods A consecutive series of 229 cases of renal cell tumors were reviewed clinically and pathologically. All cases were reclassified in accordance with the WHO classification(2004).
     方法复习229例连续肾细胞肿瘤的临床资料、大体标本、HE切片、免疫组化染色结果,按2004年WHO肾细胞肿瘤分类标准重新分类,并随访。
短句来源
  相似匹配句对
     Renal Cell Carcinoma and Tumor Vessel Formation
     细胞癌与肿瘤血管形成
短句来源
     (2) lyse tumor cells;
     溶解肿瘤细胞
短句来源
     ISLET CELL TUMORS
     胰岛细胞肿瘤
短句来源
     The Assessment of Immunity Status of Antitumor in Patients with Renal Cell Carcinoma
     细胞癌患者肿瘤免疫状况的监测
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     Relationship between mutation of tumor suppressorgene p53 and renal cell carcinoma
     肿瘤抑制基因P53突变与细胞癌的关系
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  renal cell tumors
The World Health Organization (WHO) has recently developed a new histologic classification of renal cell tumors that has demonstrated prognostic utility.
      
Molecular genetics and diagnosis of renal cell tumors
      
Experssion of the human fes cellular oncogene in renal cell tumors
      
Renal cell tumors were screened for expression of the cellular oncogenes c-abl, c-fes, c-fms, c-myc, c-ras, and c-sis in dot blot hybridization analysis.
      
Elevated concentrations of the β-subunit of S100 protein in renal cell tumors in rats
      
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Purpose: To improve the diagnosis and treatment of renal papillary renal cell carcinoma (PRCC). Methods: Clinical data of 8 cases of patients with PRCC were reviewed retrospectively and analyzed in the light of literature. Results: All 8 cases underwent radical nephrectomy. Follow up of 4 to 60 months demonstrated that 1 case died of encephalic metastasis 13 months after operation and the other 7 cases have been living without tumor. Conclusions; PRCC is a unusual renal cell carcinoma. Morphologic, cytochemical,...

Purpose: To improve the diagnosis and treatment of renal papillary renal cell carcinoma (PRCC). Methods: Clinical data of 8 cases of patients with PRCC were reviewed retrospectively and analyzed in the light of literature. Results: All 8 cases underwent radical nephrectomy. Follow up of 4 to 60 months demonstrated that 1 case died of encephalic metastasis 13 months after operation and the other 7 cases have been living without tumor. Conclusions; PRCC is a unusual renal cell carcinoma. Morphologic, cytochemical, and genotypic features of PRCC are different to that of non-PRCC. Definite diagnosis depends on imaging examination, the typical pathological and cytochemical, and genotypic features. Open operation is the treatment of choice.

目的:提高乳头状肾细胞癌的诊治水平。方法:8例均作影像学检查,IVU示患侧肾脏外形增大;CT示患侧肾脏有类圆形、界限清楚、中心有肿瘤坏死引起的低密度灶。8例患者均接受肾癌根治术,其中2例经腹腔途径,6例经11肋间切口。结果:随访4-60个月,除1例于术后13个月死于颅内转移外,其余均生存。结论:乳头状肾细胞癌是较罕见的肾细胞肿瘤,其形态学和遗传学与非乳头状肾细胞癌有明显不同;其确诊有赖于影像学检查、典型病理检查及分子遗传学特征分析;治疗仍以手术为主。

Objective To study the clinical curative effect of nephron sparing surgeries which have been performed selectively for incidental renal cell tumors less than 4cm in length.Methods Selecting the tumor size less than 4cm as the strict indication for nepron sparing surgery under in situ hypothermia anatrophic partial nephrectomy.Results Tumor size:1~2cm,3 cases;2~3cm,8 cases;3~4cm,4 cases.And en bloc removal of 0.5~1cm renal tissue together with the tumor and sent for frozen section.No blood transfusion for...

Objective To study the clinical curative effect of nephron sparing surgeries which have been performed selectively for incidental renal cell tumors less than 4cm in length.Methods Selecting the tumor size less than 4cm as the strict indication for nepron sparing surgery under in situ hypothermia anatrophic partial nephrectomy.Results Tumor size:1~2cm,3 cases;2~3cm,8 cases;3~4cm,4 cases.And en bloc removal of 0.5~1cm renal tissue together with the tumor and sent for frozen section.No blood transfusion for 10 cases and 5 cases requiring,units of 1~2 blood transfusion.Conclusion Nephron sparing surgery or partial nephrectomy in seleced cases were indicated for T_1,T_2 renal cell tumors.

目的 探讨保肾手术治疗肾肿瘤的临床疗效。方法 采取原位低温非萎陷性肾部分切除手术作为保肾术。结果 手术发现肿瘤1~2cm 3例,2~3cm 8例,3~4cm 4例。将肿瘤和正常肾组织0 . 5~1 .0cm整块切除,送冰冻切片。术后患者预后均良好。结论 保肾手术或肾部分切除术适合于浸润黏膜固有层(T1)、浸润肌层(T2 )的肾细胞肿瘤

Purpose To study the clinical and pathological features,histological classification and prognosis of renal cell tumors.Methods A consecutive series of 229 cases of renal cell tumors were reviewed clinically and pathologically.All cases were reclassified in accordance with the WHO classification(2004).Results Of 229 renal cell tumors which comprised of 89.1%(229/257) of simultaneously removed renal parenchymal neoplasms,223 cases were classified renal cell carcinoma(RCC),6 cases were oncocytoma.Of 223 RCCs,cases...

Purpose To study the clinical and pathological features,histological classification and prognosis of renal cell tumors.Methods A consecutive series of 229 cases of renal cell tumors were reviewed clinically and pathologically.All cases were reclassified in accordance with the WHO classification(2004).Results Of 229 renal cell tumors which comprised of 89.1%(229/257) of simultaneously removed renal parenchymal neoplasms,223 cases were classified renal cell carcinoma(RCC),6 cases were oncocytoma.Of 223 RCCs,cases were histologically classified into 180(accounting for 78.6% of renal cell tumors) clear cell renal cell carcinoma(CCRCC),19(8.3%) papillary renal cell carcinoma(PRCC),13(5.7%) chromophobe renal cell carcinoma(CRCC),1 case of CRCC with sarcomatoid change,6(2.6%) multilocular cystic renal cell carcinoma(MCRCC),2(0.9%) renal cell carcinomas associated with Xp11.2 translocations/TFE3 gene fusions(Xp11 RCC),2(0.9%) renal cell carcinoma unclassified,and 1(0.4%) carcinoma of the collecting ducts of Bellini(CCDB).The 5-year survival for CCRCC,PRCC was 75.5%,80%,respectively.Follow-up was available for 6 cases of CRCC and ranged from 8~57 months,and 1 died of metastasis 57 months after surgery.No evidence of recurrence and metastasis was found in MCRCC cases during the 2~40 months follow-up.Conclusions Renal cell tumors are a group of distinctive and heterogeneous entities in morphology,and malignant in the majority.CCRCC,PRCC and CRCC are the common histological subtypes.The clinical outcomes of the various subtypes are different.The new WHO classification is practical and progressive for clinical application.

目的研究肾细胞肿瘤的临床表现、组织学分型、形态学特征及预后。方法复习229例连续肾细胞肿瘤的临床资料、大体标本、HE切片、免疫组化染色结果,按2004年WHO肾细胞肿瘤分类标准重新分类,并随访。结果229例肾细胞肿瘤占同期肾实质肿瘤89.1%(229/257),其中223例(97.4%)为肾细胞癌,6例(2.6%)为肾嗜酸细胞腺瘤。肾细胞癌中,透明细胞癌180例(78.6%),乳头状肾细胞癌19例(8.3%),嫌色细胞癌13例(5.7%),1例嫌色细胞癌伴肉瘤变,多房性囊性肾细胞癌6例(2.6%),Xp11.2易位/TFE3基因融合相关肾细胞癌2例(0.9%),未能分类的肾细胞癌2例(0.9%),集合管癌1例(0.4%)。透明细胞癌5年生存率为75.5%;乳头状肾细胞癌5年生存率为80%;嫌色细胞癌随访6例,随访期8~57个月,1例于57个月后死于肿瘤转移;多房性囊性肾细胞癌随访2~40个月,无复发和转移。结论肾细胞肿瘤是一组形态学上各有特征的异质性肿瘤,以恶性为主,其中透明细胞癌、乳头状肾细胞癌、嫌色细胞癌最常见。不同类型肾细胞癌预后不同。WHO肾...

目的研究肾细胞肿瘤的临床表现、组织学分型、形态学特征及预后。方法复习229例连续肾细胞肿瘤的临床资料、大体标本、HE切片、免疫组化染色结果,按2004年WHO肾细胞肿瘤分类标准重新分类,并随访。结果229例肾细胞肿瘤占同期肾实质肿瘤89.1%(229/257),其中223例(97.4%)为肾细胞癌,6例(2.6%)为肾嗜酸细胞腺瘤。肾细胞癌中,透明细胞癌180例(78.6%),乳头状肾细胞癌19例(8.3%),嫌色细胞癌13例(5.7%),1例嫌色细胞癌伴肉瘤变,多房性囊性肾细胞癌6例(2.6%),Xp11.2易位/TFE3基因融合相关肾细胞癌2例(0.9%),未能分类的肾细胞癌2例(0.9%),集合管癌1例(0.4%)。透明细胞癌5年生存率为75.5%;乳头状肾细胞癌5年生存率为80%;嫌色细胞癌随访6例,随访期8~57个月,1例于57个月后死于肿瘤转移;多房性囊性肾细胞癌随访2~40个月,无复发和转移。结论肾细胞肿瘤是一组形态学上各有特征的异质性肿瘤,以恶性为主,其中透明细胞癌、乳头状肾细胞癌、嫌色细胞癌最常见。不同类型肾细胞癌预后不同。WHO肾细胞癌的组织学分型有其实用性和先进性。

 
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