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   pheochromocytoma 在 泌尿科学 分类中 的翻译结果: 查询用时:0.009秒
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pheochromocytoma
相关语句
  嗜铬细胞瘤
    The diagnosis and treatment of pheochromocytoma of the urinary bladder
    膀胱嗜铬细胞瘤的诊断和治疗
短句来源
    Pheochromocytoma of Urinary Bladder,Report of 7 Cases
    膀胱嗜铬细胞瘤(附7例报告)
短句来源
    Diagnosis and treatment of pheochromocytoma of the urinary bladder
    膀胱嗜铬细胞瘤的诊断和治疗
短句来源
    Diagnosis and treatment of pheochromocytoma in urinary bladder
    膀胱壁内嗜铬细胞瘤的诊断与治疗
短句来源
    Diagnosis and treatment of pheochromocytoma in urinary bladder
    膀胱嗜铬细胞瘤的诊断与治疗
短句来源
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  “pheochromocytoma”译为未确定词的双语例句
    Coexisting primary aldosteronism and pheochromocytoma (report of 4 cases)
    肾上腺皮髓质混合性病变(附四例报告)
短句来源
    In only 1 cases the adrenal tumor was metastatic from the renal cell carcinoma,the other 2 being an adrenal adenoma and a pheochromocytoma.
    1例肾癌并发肾上腺转移癌者术后随访2年,健在。
短句来源
    Results Multiple position radioimmunoimaging and single position radio immunoimaging showed radioactivity concentration area at bladder cancer and no radioactivity concentration for normal bladder except in 1 case with pheochromocytoma of the bladder. The tumors can be detected as small as less than 1.0cm in diameter. Sensitivity was 94.1 %,and specificity 87.5%.
    结果 膀胱癌患者不同体位γ显像在肿瘤部位有明显放射性浓聚 ,膀胱癌显像阳性率 (灵敏度 )为 94.1% ,特异性为 87.5 %。
短句来源
    Methods The clinical data of 4 cases of coexisting primary aldosteronism and pheochromocytoma were retrospectively analyzed.
    方法 回顾分析 4例肾上腺皮髓质混合性病变资料。
短句来源
    Two cases were preoperatively suspected of having bladder pheochromocytoma and took α-receptor blocker for 2 weeks.
    术前确诊 2例 ,口服α受体阻滞剂 2周。
短句来源
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  pheochromocytoma
Effects of Human Presenilin 1 Isoforms on Proliferation and Survival of Rat Pheochromocytoma Cell Line PC12
      
Influence of phospholipases A2 from snake venoms on survival and neurite outgrowth in pheochromocytoma cell line PC12
      
Thyroidectomy was performed in four asymptomatic carriers of RET mutations from three MEN 2A families (in two families, affected relatives had bilateral pheochromocytoma).
      
Pheochromocytoma patients had more pronounced perioperative BP oscillations, needed more antihypertensive drugs, analgesics and required prolonged hospital stay than patients with other adrenal tumors.
      
Diagnosis and treatment of pheochromocytoma in urinary bladder
      
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Phcochromocytoma of the urinary bladder is a rare disease, which probably accounts for Jess than 0.06 percent of all tumors of the urinary bladder We report 4 cases of vesical pheochromocytoma, among which, one is benign; 3 are malignant, and one of them associated with pregnancy. The importance of preoperative localization and aggressive .operative treatment are emphasized. After operation, the patients should closely be fol]owed-up in order to watch out for the recurrence or metastasis of the tumor

膀胱嗜铬细胞瘤罕见,约占全部膀胱肿瘤的0.06%。我们报告了4例膀胱嗜铬细胞瘤,其中1例良性、3例恶性,且1例为妊娠合并嗜铬细胞瘤。本文强调了术前定位诊断的重要性和积极的外科手术治疗方法,术后应密切随诊,警惕肿瘤转移和复发。

Pheochromocytoma of the urinary bladder is a rare type of extraadrenal pheo-chromocytoma.Seven cases of pheochromocytoma of the urinary bladder were reported.The characteristic clinical manifestations are hypertension,micturitional attacks in-cluding headache,palpitation,hematuria,blurred vision dr sweating.Preoperativediagnosis can be established by the determination of elevated levels of catecholamineand their metabolites in blood and urine.Computed tomography is the recommendedinitial localizing procedure...

Pheochromocytoma of the urinary bladder is a rare type of extraadrenal pheo-chromocytoma.Seven cases of pheochromocytoma of the urinary bladder were reported.The characteristic clinical manifestations are hypertension,micturitional attacks in-cluding headache,palpitation,hematuria,blurred vision dr sweating.Preoperativediagnosis can be established by the determination of elevated levels of catecholamineand their metabolites in blood and urine.Computed tomography is the recommendedinitial localizing procedure in anatomic localization.Treatment is surgical removalof the tumor in the urinary bladder,most patients can be cured by surgery.

膀胱嗜铬细胞瘤为一种罕见的异位嗜铬细胞瘤,本文报告了我院收治的7例。膀胱嗜铬细胞瘤最具特征性的临床表现是与排尿有关的高血压发作,及头痛、心悸、血尿、视物模糊或大汗。通过测定血、尿中升高的儿茶酚胺及其代谢产物可确立术前诊断,定位诊断则首推 CT检查。膀胱嗜铬细胞瘤的治疗为手术切除肿瘤,大多数病人可获痊愈。

Diagnosis and management of 27 cases of adrenal tumor and hyperplasia have been presented in this paper,which included 8 cases of Cushing's syndrom,16 cases of pheochromocytoma,1 case of primary aldosteronism,1 case of medulla hyperplasia and 1 case of non-functioning adrenal tumor. The level diagnosis was mainly by means of CT and retroperitoneal pneumography.All the patients were mainly treated by surgical operations.Experimence in the management has been discussed.

27例肾上腺肿瘤及增生中皮质醇症8例、嗜铬细胞瘤16例、原发性醛固酮增多症、髓质增生症及无功能性肿瘤各1例。定位诊断主要为CT检查及腹膜后注气造影。皮质醇症术前应有效地控制血糖;嗜铬细胞瘤术前使用皮质激素有助于患者顺利地度过手术关。本组患者以手术治疗为主,并阐述了手术治疗的经验。

 
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