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囊性
相关语句
  cystic
    Cystic Partially Differentiated Nephroblastoma
    囊性部分分化性肾母细胞瘤
短句来源
    Multilocular cystic nephroma
    多房囊性肾瘤
短句来源
    CT diagnosis of cystic renal carcinoma
    囊性肾癌的CT诊断
短句来源
    Pathological results included renal clear cell carcinoma in 117 patients,cystic renal cell carcinoma in 3 patients,renal pelvis transitional cell carcinoma in 2 patients,chromophobe carcinoma in 1 patient,hamartoma in 2 patients,and oxyphil cell tumor in 1 patient.
    病理报告:117例肾透明细胞癌,3例囊性肾细胞癌,2例肾盂移行细胞癌,1例嫌色细胞癌,2例错构瘤,1例嗜酸细胞瘤。
短句来源
    Multilocular cystic nephroma
    多房性囊性肾瘤
短句来源
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  “囊性”译为未确定词的双语例句
    Detection of fibrosis transmembrane conductance regulator gene⊿F508 mutation in Chinese patients with congenital bilateral absence of vas deferens
    先天性双侧输精管缺如患者囊性纤维化跨膜转运调节物基因⊿F508突变的研究
短句来源
    Results:Among all 25 cases,transitional cell carcinoma was confirmed in 8 cases,renal cell carcinoma in 16 cases,renal embryonal cancer in 1 case.
    结果 :2 5例囊性肾恶性肿瘤中肾盂移行细胞癌 8例 ,肾细胞癌 16例 ,肾胚胎癌 1例。
短句来源
    Results:Renal cysts were identified by preoperative ultrasonography, computerized tomography and magnetic resonance imaging in 37%(22/59)、24%(15/61) and 35%(6/17) respectively.
    结果:B超、CT和MRI在诊断肾癌合并有肾囊肿病例时,检查出肾囊肿的准确性分别为37%、24%和35%,而全部64例病理检查中又查出15例(23%)囊性占位性病变;
短句来源
    Gro ssly,the tumor exhibited a 7.9 cm×8.9 cm×9.0 cm multilocular cyst full of coff ee- colored mucoid fluid with varying size ranging from 0.5 to 2.0 cm. Focall y thick-walled cysts with solid areas were seen.
    术后见左肾上极7.9cm×8.9cm×9.0cm多房囊性肿瘤,边界清楚,内充满咖啡色粘稠液体,囊腔直径0.5~2.0cm,部分囊壁较厚呈实性。
短句来源
    T1 in 8 and T2 in 1. Nuclear grade and pathological stage were lower in those with CRCC than in those with RCC (P=0. 0001, 0.045).
    肿瘤分期T1期8例(88.9%)、T2期1例(11.1%),均低于同期非囊性肾细胞癌(P=0.000 1和0.045)。
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  cystic
The Mutation Spectrum of the CFTR Gene in Cystic Fibrosis Patients from Bashkortostan
      
Mutations of CFTR were studied in patients with cystic fibrosis (CF) from Bashkortostan.
      
Polymorphisms of the Cytochrome P450 (CYP1A1, CYP2E1) and Microsomal Epoxide Hydrolase (mEPHX) Genes in Cystic Fibrosis and Chro
      
Frequencies of CYP1A1, CYP2E1, and mEPHX polymorphic variants were analyzed in cystic fibrosis, chronic obstructive lung disease, bronchiectatic disease, chronic nonobstructive bronchitis, and recurring bronchitis.
      
Mutations in CYP1A1 and mEPHX were shown to modify the severity of respiratory disorders in cystic fibrosis, the combination of CYP1A1 genotype Val/Val with the "very slow" mEPHX phenotype being most unfavorable (odds ratio OR = 12.30).
      
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Two cases of cystic partially differentiated nephroblastoma are reported, Grossly, the lesion is polycystic in appearance. Microscopically the cysts vary in size and are lined by cuboidal or flattened epithelial cells. Highly differentiated nephroblastoma elements can be seen in the septa of the cysts. This tumor may have its origin in the metanephrogenic blastoma, occurs frequently in children under 2 years of age, and is benign in nature. Quite a few terms have been applied to this disease, however in the...

Two cases of cystic partially differentiated nephroblastoma are reported, Grossly, the lesion is polycystic in appearance. Microscopically the cysts vary in size and are lined by cuboidal or flattened epithelial cells. Highly differentiated nephroblastoma elements can be seen in the septa of the cysts. This tumor may have its origin in the metanephrogenic blastoma, occurs frequently in children under 2 years of age, and is benign in nature. Quite a few terms have been applied to this disease, however in the author's opinion, the term cystic partially differentiated nephroblastoma seems to be appropriate. It should be classified as a subgroup of nephroblastoma.

本文报告2例罕见的儿童肾肿瘤。大体特征为多囊。镜下,囊大小不一,多由立方形到扁平上皮细胞衬覆;囊之间的间隔中,见典型肾母细胞瘤的某些成分,但分化较高、量较少。组织发生,可能与肾母细胞瘤相同,起源于后肾胚芽。该瘤多见于2岁以下儿童,绝大多数为良性。文献中名称甚多,以称囊性部分分化性肾母细胞瘤较为恰当,可列为肾母细胞瘤的亚型。

Multilocular cystic nephroma(MCN)is a very rare renal tumor. Histogenesis of the tumor has not been clarified and the designation has been confused. Both the clinical and pathologic manifestations are similar to nephroblastoma and renal cystic diseases in some ways. The prognosis is very good.

多房囊性肾瘤是十分罕见的肾脏肿瘤,其组织起源不清,命名混乱,临床表现和病理形态学与肾母细胞瘤以及多囊性肾脏病变有相似之处,而治疗和预后与Wilm’s瘤却有很大差别。本文报告1例,综合文献对其命名、组织发生和病变性质、病理特征、鉴别诊断、治疗及其预后进行讨论。

Malignant rhabdoid tumor of thekidney is rare.This paper reports 2cases proved pathologically.It is hig-hly malignant with distinctive clinicalcomputed tomographic and pathologicfeatures.The CT characteristic findi-ngs included extensive destruction ofrenal parenchyma and forming a mai-nly cystic lesion with central soft-masslike“melting ice”.Subcapsular fluidcollection and invasive nodules wereobserved.In addition,the renal pelviswas also involved frequently.

肾恶性横纹肌样瘤是一罕见的高度恶性肿瘤,临床、CT和病理表现均有特殊之处。本文报告2例,均经病理诊断。作者认为肾脏广泛破坏,形成以囊性变为主并存“溶冰状”改变的软组织肿块,累及肾盂、伴肾包膜侵袭结节和肾包膜下积液是本病的CT特点。

 
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