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carcinoma syndrome
相关语句
  癌综合征
     Clinicopathological analysis of 55 patients with normal-sized ovary carcinoma syndrome
     卵巢正常大小的癌综合征55例临床病理分析
短句来源
     Objective To investigate the clinical characteristics and prognostic factors of the primary normal sized epithelial ovarian carcinoma syndrome.
     目的 探讨卵巢正常大小的原发性卵巢上皮性癌综合征的临床特点及预后因素。
短句来源
     Analysis of the Clinical Characteristics and Prognostic Factors with Primary Normal-sized Epithelial Ovarian Carcinoma Syndrome
     卵巢正常大小的原发性卵巢上皮性癌综合征的临床特点与预后影响因素
短句来源
     Objective To summarize the clinicopathological features,survival rate and prognosis of 55 patients with normal-sized ovary carcinoma syndrome(NOCS),and analyze the expressions of molecular markers of NOCS.
     目的探讨卵巢正常大小的癌综合征(NOCS)临床病理特征、存活率及预后影响因素,分析NOCS分子标志物的表达。
短句来源
     Diagnosis of Primary Normal-sized Epithelial Ovarian Carcinoma Syndrome by Transvaginal Color Doppler Sonography
     阴道超声诊断卵巢正常大小的原发性卵巢上皮性癌综合征的临床价值
短句来源
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  “carcinoma syndrome”译为未确定词的双语例句
     Clinical analysis of normal-sized primary ovary carcinoma syndrome in 16 cases
     16例卵巢正常大小的原发性卵巢上皮癌综合征的临床分析
短句来源
     Objective To evaluate clinical-pathologic features,diagnostic criteria,effetctive treatmetna and prognosis of a clinically rare"normal-sized ovary carcinoma syndrome".
     目的探讨正常大小卵巢综合征(normal-sized ovary carcinoma syndrome,NOCS)的临床特点、诊断标准及预后。
短句来源
     Normal sized ovary carcinoma syndrome Clinical and pathological analysis of 11 cases
     11例正常大小卵巢癌综合征的临床及病理分析
短句来源
     Ki-67 expression in nevoid basal cell carcinoma syndrome associated odontogenic keratocysts
     基底细胞痣综合征的牙源性角化囊肿中Ki-67表达的研究
短句来源
     Clinical and pathological analysis of 22 cases of normal-sized ovary carcinoma syndrome
     22例卵巢正常大小卵巢癌综合征的临床诊断及病理分析
短句来源
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  相似匹配句对
     SYNDROME
     Noonan氏综合征(附2例报告)
短句来源
     THE CAVERNOUS SINUS SYNDROME AND NASOPHARYNGEAL CARCINOMA
     海绵窦综合征与鼻咽癌
短句来源
     NORMAL SIZED OVARY CARCINOMA SYNDROME
     正常大小卵巢癌综合征
短句来源
     Mirizzi Syndrome
     Mirizzi's综合征
短句来源
     Nursing of carcinoma
     肿瘤的护理
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  carcinoma syndrome
Mutations at 15q13-14 are associated with the colorectal adenoma and carcinoma syndrome (CRAC) described in Ashkenazi families.
      
With identification of the Hedgehog receptor PTCH1 as a tumour suppressor gene that underlies the human nevoid basal cell carcinoma syndrome (NBCCS), the Hedgehog signalling pathway was firmly linked to cancer.
      
Mutations in the human homologue of the Drosophila patched gene (PTCH) are responsible for the hereditary disorder called nevoid basal cell carcinoma syndrome (NBCCS).
      
In this study, we used newly designed high-resolution oligonucleotide microarrays with a median distance between the probes of 776?bp (average probe interval 2,271?bp) to detect gene deletions in nevoid basal cell carcinoma syndrome (NBCCS) patients.
      
We have previously identified the human homologue of the Drosophila patched gene and have described, in this gene, mutations that give rise to naevoid basal cell carcinoma syndrome (NBCCS).
      
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Objective To evaluate clinical pathologic features, diagnostic criteria, effective treatment and prognosis of a clinically rare “normal sized ovary carcinoma syndrome”. Methods Histologic slides of 11 cases from 1984 to 1993 of normal sized ovary carcinoma syndrome were retrospectively reviewed. Seven of the 11 cases were extraovarian peritoneal serous papillary carcinoma(EPSPC). The remaining 4 cases were serous adenocarcinoma of the ovary (2 cases), malignant mesothelioma (1 case) and...

Objective To evaluate clinical pathologic features, diagnostic criteria, effective treatment and prognosis of a clinically rare “normal sized ovary carcinoma syndrome”. Methods Histologic slides of 11 cases from 1984 to 1993 of normal sized ovary carcinoma syndrome were retrospectively reviewed. Seven of the 11 cases were extraovarian peritoneal serous papillary carcinoma(EPSPC). The remaining 4 cases were serous adenocarcinoma of the ovary (2 cases), malignant mesothelioma (1 case) and metastatic poorly differentiated adenocarcinoma of unknown origin (1 case). All patients received relatively thorough surgical resection combined with multiple courses of adjuvant chemotherapy. Results The patient with malignant mesothelioma survived for 90 months, one case with EPSPC survived for 87 months up to Dec 1997. The average survival time of 9 patients who died of their diseases was 17.8 months, being longer than that reported in the literature. Conclusion Following accurate diagnosis of normal sized ovary carcinoma syndrome, radical tumor resection is the first treatment of choice. For residual tumor, postoperative chemotherapy or radiotherapy is essential to obtain better prognosis.

目的探讨正常大小卵巢癌综合征的临床特点、诊断标准、有效的治疗方法及其预后。方法回顾性分析1984~1993年在我院治疗及病理复核证实的11例正常大小卵巢癌综合征,其中7例为性腺外苗勒氏管肿瘤,也称卵巢外腹膜浆液性乳头状腺癌(EPSPC),2例卵巢浆液性腺癌,1例恶性间皮瘤,1例原发灶不明的转移性腺癌。上述无论何种类型,均宜最大限度切除肿瘤,术后残存肿瘤<2cm,并辅以有效多程综合化疗。结果1例恶性间皮瘤存活90个月,随访至1997年6月仍健在。1例EPSPC已存活87个月,随访至1997年11月仍健在。9例已死亡患者平均生存17.8个月,比文献报道存活时间长。结论对此综合征患者必须高度重视鉴别诊断,首选手术治疗,尽量切除癌灶(残存肿瘤<2cm),术后辅以有效化疗或放疗,以获得最佳生存和预后。

Objective To investigate the clinical characteristics and prognostic factors of the primary normal sized epithelial ovarian carcinoma syndrome. Methods The clinical records and pathologic slides of the 10 patients who satisfied the diagnostic criteria were retrospectively analyzed. Results The primary normal sized epithelial ovarian carcinoma syndrome was detected in approximately 1.92% of the patients with the epithelial ovarian carcinoma .The age of the patients at diagnosis ranged...

Objective To investigate the clinical characteristics and prognostic factors of the primary normal sized epithelial ovarian carcinoma syndrome. Methods The clinical records and pathologic slides of the 10 patients who satisfied the diagnostic criteria were retrospectively analyzed. Results The primary normal sized epithelial ovarian carcinoma syndrome was detected in approximately 1.92% of the patients with the epithelial ovarian carcinoma .The age of the patients at diagnosis ranged from 43~70 years, with a median age of 57 years. The most common presentations included anorexia, increasing abdominal girth and awareness of abdominal or pelvic mass. During the exploratory laparotomy although we often discovered the diffuse metastasis throughout the abdominal and pelvic cavity, the ovaries both appeared normal size and had a fine granularity on the external surface. The survival time of patients with remained tumors smaller than 2.0 cm was longer than those with remained tumors larger than 2.0 cm, but the Log rank evaluation indicated χ 2=0.61, P >0.05. The patients who underwent postoperative chemotherapy have been noted to achieve some long term survival. The median survival time was 20 months. Conclusion The results predict that the size of the remained tumors may be one of the important factors to the survival and the disease is sensitive to the postoperative chemotherapy.

目的 探讨卵巢正常大小的原发性卵巢上皮性癌综合征的临床特点及预后因素。方法 对 10例患者的病例资料采用回顾性分析方法。结果 本病多发生于 5 0岁以上 ,占 80 % ;以腹胀、食欲差为首发症状 ,占 90 % ;就诊晚 ,易误诊 ,误诊率 40 % ;卵巢均正常大小 ,盆腹腔有广泛种植 ,局部聚集成块 ,占 70 % ;术后残留灶直径 <2 .0cm患者的生存时间高于术后残留灶直径≥ 2 .0cm者 ,但差异无显著性 (P >0 .0 5 )。化学治疗疗程数≥ 6个者生存时间明显高于疗程数 <6个者 (P <0 .0 5 )。本组患者中位生存时间 2 0个月 ,2年存活率 5 0 % ;3年存活率 30 % ;5年存活率 2 0 %。结论 术后残留灶大小可能是影响卵巢正常大小的原发性卵巢上皮性癌综合征患者预后的重要因素。术后系统化学治疗疗效显著

Objective To improve the recognition of the hereditary nonpolyposis colorectal cancer(HNPCC) in its essence. Methods A survey of 4 pedigrees of HNPCC patients was made. Results Among the 4 families, 14 persons had colorectal cancer. The average age of the cancer onset was 43 years(from 26 to54).61.9%(13/21) of the foci were located in the proximal colon to the splenic flexure. The patients having multifocal colorectal cancer account for 35.7% (5/14) of all cases.No colorectal polyposis was found in all...

Objective To improve the recognition of the hereditary nonpolyposis colorectal cancer(HNPCC) in its essence. Methods A survey of 4 pedigrees of HNPCC patients was made. Results Among the 4 families, 14 persons had colorectal cancer. The average age of the cancer onset was 43 years(from 26 to54).61.9%(13/21) of the foci were located in the proximal colon to the splenic flexure. The patients having multifocal colorectal cancer account for 35.7% (5/14) of all cases.No colorectal polyposis was found in all cases. One of the four families had the familial carcinoma syndrome. Conclusions HNPCC patients and their family members should be followed up regularly for early diagnosis and treatment of the disease and for better prognosis.

目的 :提高对遗传性非息肉病性大肠癌本质的认识。 方法 :对四个有遗传性非息肉病性大肠癌家系进行调查。结果 :四家系共有 14例病人 ,发病时平均年龄 43岁。 6 1.9% (13/ 2 1)的癌灶位于脾曲近端的大肠。大肠多原发癌占 35 .7% (5 /14)。无结肠息肉病。四家系中之一为癌家族综合征。 结论 :对遗传性非息肉病性大肠癌病人及其家系成员要进行严密监测 ,争取疾病早诊断早治疗 ,提高治疗效果。

 
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