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纤维瘤
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  fibroma
    Eleven of 28 patients (39 3%) were benign tumors with 4 kinds of histologic types including 2 cases of cavarnous hemangioma, 1 case of fibroma, 1 case of leiomyoma, 7 cases of pheochromocytom.
    良性 1 1例 (占 39 3 % ) ,有 4种病理类型 ,分别为膀胱海绵状血管瘤、膀胱壁纤维瘤、膀胱平滑肌瘤、膀胱嗜铬细胞瘤。
短句来源
    One case:right testicle fibroma with calcification
    右睾丸纤维瘤伴钙化1例
短句来源
    One Case:Renal Fibroma
    肾纤维瘤1例报告
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  “纤维瘤”译为未确定词的双语例句
    Solitary fibrous tumor of the prostate(report of 2 cases)
    前列腺孤立性纤维瘤二例报告
短句来源
    Clinicopathologic analysis of solitary fibrous tumor of kidney
    肾孤立性纤维瘤临床病理观察
短句来源
    Objective To investigate the diagnosis and treatment of solitary fibrous tumor of the prostate.
    目的探讨前列腺孤立性纤维瘤的诊断和治疗。
短句来源
    Methods Two case of solitary fibrous tumor of the prostate were reviewed retrospectively.
    方法总结2例前列腺孤立性纤维瘤患者资料。
短句来源
    Objective To explore the clinical pathological features,diagnosis and differential diagnoses of solitary fibrous tumor (SFT) of the kidney.
    目的探讨肾孤立性纤维瘤的临床病理特征、诊断和鉴别诊断,提高对该肿瘤的诊断水平。
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  fibroma
The structure of these tumorlike formations is characteristic of fibroma.
      
An unusual sphenoid ridge tumor: Cementifying fibroma
      
Value of dynamic enhanced MR imaging for the differential diagnosis between ovarian fibroma and subserosal leiomyoma
      
These included hemangiomas and metastatic cancer (previously identified in dinosaurs), desmoplastic fibroma, and osteoblastoma.
      
CT and MRI of congenital sinonasal ossifying fibroma
      
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Objective To summarize the experience in the diagnosis and treatment of non epithelial tissue tumor of urinary bladder. Methods From 1953 to April 2002, a total of 28 patients with non epithelial sissue tumor in 3 925 bladder tumor cases were analyzed. Results Painless gross hematuria, pelvic mass, urinary frequency and dysuria are systoms of non epithelial bladder tumor. Ultrasonic examination, computed tomography (CT) scan, cystoscopy and biopsy is used for diagnosis of the tumor. Seventeen of 28 patients...

Objective To summarize the experience in the diagnosis and treatment of non epithelial tissue tumor of urinary bladder. Methods From 1953 to April 2002, a total of 28 patients with non epithelial sissue tumor in 3 925 bladder tumor cases were analyzed. Results Painless gross hematuria, pelvic mass, urinary frequency and dysuria are systoms of non epithelial bladder tumor. Ultrasonic examination, computed tomography (CT) scan, cystoscopy and biopsy is used for diagnosis of the tumor. Seventeen of 28 patients (61 7%) were malignant neoplasms in 7 kinds of pathologic types, which was small cell carcinoma(5 cases), rhabdomyosarcoma (4 cases), leiomyosarcoma (4 cases), lymphoma (1 case), malignant fibrous histiocytoma (1 case), liposarcoma(1 case), melanoma (1 case) respectively. Eleven of 28 patients (39 3%) were benign tumors with 4 kinds of histologic types including 2 cases of cavarnous hemangioma, 1 case of fibroma, 1 case of leiomyoma, 7 cases of pheochromocytom. All benign tumor patients were treated with partial cystectomy, transurethral bladder tumor resect (TURBT) and fulguration. In 17 malignant neoplasms patients, 7 of them received partial cystectomy, 9 received radical cystectomy, and 1 patient′s tumor was unresectable. Those malignant bladder tumor patient are followed up, but 3 years survival rates is only 8/17. Conclusions Non epithelial tissue tumor of the urinary bladder is rare with complicated pathologic types. Malignant neoplasms are more than benign tumors with very poor prognosis, benign tumors′ prognosis is good. Diagnosis rate which was confirmed before operation is low. Dip biopsy under cystoscopy may enhance the diagnosis rate. Surgical treatment is the main therapy for non epithelial tissue tumor of the urinary bladder. Because of the aggressive biologic behavior of malignant tumors, they should be identified promptly and treated appropriately. According to the histologic appearance radiotherapy and chemotherapy is mandatory in some cases.

目的 总结膀胱非上皮性肿瘤的诊治经验。 方法 对 1 953~ 2 0 0 2年收治的 2 8例膀胱非上皮性肿瘤患者的诊治情况进行总结、分析。 结果 膀胱非上皮性肿瘤的主要临床表现为血尿、盆腔肿块、尿频、排尿困难等症状。主要辅助检查为B超、CT、膀胱镜检查及镜下活检。本组 2 8例中 ,经术后病理检查 ,恶性肿瘤 1 7例 (占 61 7% ) ,有 7种病理类型 ,分别为膀胱横纹肌肉瘤、膀胱小细胞癌、膀胱平滑肌肉瘤、膀胱恶性淋巴瘤、膀胱恶性纤维组织细胞瘤、膀胱脂肪肉瘤、膀胱黑色素瘤 ;良性 1 1例 (占 39 3 % ) ,有 4种病理类型 ,分别为膀胱海绵状血管瘤、膀胱壁纤维瘤、膀胱平滑肌瘤、膀胱嗜铬细胞瘤。 1 1例良性肿瘤均完整切除或电灼、电切。 1 7例恶性肿瘤中 ,膀胱部分切除术 7例、膀胱全切除术 9例、无法切除 1例 ,有 7例恶性肿瘤因复发多次行手术切除。 1 7例恶性肿瘤患者均获随访 ,3年存活率 47 0 % (8/ 1 7)。 结论 膀胱非上皮性肿瘤临床少见 ,病理类型复杂 ,恶性居多且预后较差 ,良性肿瘤预后较好。术前诊断率低 ,膀胱镜下深部活检可提高诊断率。手术是该...

目的 总结膀胱非上皮性肿瘤的诊治经验。 方法 对 1 953~ 2 0 0 2年收治的 2 8例膀胱非上皮性肿瘤患者的诊治情况进行总结、分析。 结果 膀胱非上皮性肿瘤的主要临床表现为血尿、盆腔肿块、尿频、排尿困难等症状。主要辅助检查为B超、CT、膀胱镜检查及镜下活检。本组 2 8例中 ,经术后病理检查 ,恶性肿瘤 1 7例 (占 61 7% ) ,有 7种病理类型 ,分别为膀胱横纹肌肉瘤、膀胱小细胞癌、膀胱平滑肌肉瘤、膀胱恶性淋巴瘤、膀胱恶性纤维组织细胞瘤、膀胱脂肪肉瘤、膀胱黑色素瘤 ;良性 1 1例 (占 39 3 % ) ,有 4种病理类型 ,分别为膀胱海绵状血管瘤、膀胱壁纤维瘤、膀胱平滑肌瘤、膀胱嗜铬细胞瘤。 1 1例良性肿瘤均完整切除或电灼、电切。 1 7例恶性肿瘤中 ,膀胱部分切除术 7例、膀胱全切除术 9例、无法切除 1例 ,有 7例恶性肿瘤因复发多次行手术切除。 1 7例恶性肿瘤患者均获随访 ,3年存活率 47 0 % (8/ 1 7)。 结论 膀胱非上皮性肿瘤临床少见 ,病理类型复杂 ,恶性居多且预后较差 ,良性肿瘤预后较好。术前诊断率低 ,膀胱镜下深部活检可提高诊断率。手术是该病的主要治疗方法。良性肿瘤应完整切除 ,恶性肿瘤应争取广泛切除 ,结合其病理特点辅助放化疗可能提高疗效

Objective: To improve the diagnosis,therapy and prognosis of testicular tumor in Mengolian men.Methods: A retrospective review of 35 cases of testicular tumors in Mengolian men from seven medical centers dated from 1990 to 2004 was performed.Results: The usual presentation of a testicular tumor was a nodular or painless swelling of one gonad.The mean delay in diagnosis was(40.03)±(53.45) weeks.For 16 patients,delay in diagnosis was more than or equal to six months.The histologic composition of this series was...

Objective: To improve the diagnosis,therapy and prognosis of testicular tumor in Mengolian men.Methods: A retrospective review of 35 cases of testicular tumors in Mengolian men from seven medical centers dated from 1990 to 2004 was performed.Results: The usual presentation of a testicular tumor was a nodular or painless swelling of one gonad.The mean delay in diagnosis was(40.03)±(53.45) weeks.For 16 patients,delay in diagnosis was more than or equal to six months.The histologic composition of this series was 21(60%) seminoma,10((28.6)%) nonseminoma,2((5.7)%) lymphoma,1((2.35)%) fibroneuroma and 1((2.35)%) liomyoma.Regarding stage,22,2,and 5 of 29 germ cell tumors were seen initially as stage I,II,and III,respectively.Combined therapy,including radical orchiectomy,radiotherapy and chemotherapy,were taken.29 cases have been followed for 2 months to 10 years,4 out of them died of distant matastasis,one died of other disease,one lives with tumor,the others live without relapse and metastasis. Three and 5-year survival rates for Mengolian patients with seminoma and nonseminoma were(95.0)%,(95.0)%,(57.1)% and(42.8)%,respectively. Conclusion: In this article,the rate of seminoma to germ cell tumors is higher than that of general population.There is an increased mean delay in diagnosis for Mengolian patients.Three and 5-year survival rates for nonseminoma are lower than that for seminoma.Better public awareness regarding testicular tumor in this population,advances in diagnosis and therapy will help to improve therapeutic effectiveness and prognosis.

目的:提高对蒙古族睾丸肿瘤的诊断和治疗水平。方法:多中心回顾性分析1990年2月~2004年12月35例蒙古族睾丸肿瘤患者的临床资料。结果:主要症状为无痛性睾丸肿大或结节。平均延误诊断(40.03±53.45)周,16例(45.7%)延迟诊断6个月~5年。睾丸肿瘤病理类型:精原细胞瘤21例(60%),占生殖细胞瘤的67.7%(21/31),非精原细胞瘤10例(28.6%),恶性淋巴瘤2例(5.7%),神经纤维瘤和平滑肌瘤各1例(5.7%)。生殖细胞瘤I期22例,II期2例,III期5例。治疗手段以睾丸肿瘤根治性切除和放疗及化疗为主。随访29例睾丸恶性肿瘤患者2个月~10年,其中精原细胞瘤20例,3、5年生存率分别为95.0%、95.0%;非精原细胞瘤7例,3、5年生存率分别为57.1%、42.8%;2例恶性淋巴瘤患者,1例健在,1例化疗中。结论:本组蒙古族睾丸肿瘤患者精原细胞瘤比例高于一般人群,平均延误诊断时间较长。非精原细胞瘤患者3、5年生存率均低于精原细胞瘤患者。睾丸肿瘤知识的宣教和诊疗技术的提高,有助于改善睾丸肿瘤患者的疗效和预后。

Objective To investigate the diagnosis and treatment of solitary fibrous tumor of the prostate.Methods Two case of solitary fibrous tumor of the prostate were reviewed retrospectively.One case was a 40-year-old man presenting with dysuria and perineal swelling pain gradually.B-ultrasound showed enlarged prostate with well-defined margin.The serum PSA was 1.92 ng/ml.Urodynamic study dis- played lower urinary tract obstruction curve.The other case was a 56-year-old man presenting with frequent and urgent urination,and...

Objective To investigate the diagnosis and treatment of solitary fibrous tumor of the prostate.Methods Two case of solitary fibrous tumor of the prostate were reviewed retrospectively.One case was a 40-year-old man presenting with dysuria and perineal swelling pain gradually.B-ultrasound showed enlarged prostate with well-defined margin.The serum PSA was 1.92 ng/ml.Urodynamic study dis- played lower urinary tract obstruction curve.The other case was a 56-year-old man presenting with frequent and urgent urination,and nocturia.Uneven prostatic hyperplasia in texture was indicated by B-ultrasound and CT.After prostatic paracentesis biopsy,the patient refused operation and resorted to radiotherapy and he was lost to follow-up.Their clinical data were analyzed in combination with the relevant literature.Results Case 1 was diagnosed with solitary fibrous tumor of the prostate and underwent transurethral resection of the prostate(TUBP)with 83g prostatic tissue resected.The patient was followed for 8 months with good voiding and no sign of recurrence.Case 2 was lost to follow-up.Pathology showed that the tumors were composed of mixture of spindle cells with dense collagenous bands in both cases.Microscopically,characteristic myxoid changes and hemangiopericytoma-like area of solitary fibrous tumor of the prostate were observed.In case 1, the mitotic rate was 1/10 hlgh-power field(HPF).Immunohistochemical test result was positive for CD_(34), CD_(99) and bcl-2,negative for S-100 and SM-A.Case 2 was diagnosed with malignant solitary fibrous tumor of the prostate.Pathology showed the mitotic rate of 4/10 HPF.Immunohistochemical test result was positive for CD_(34),CD_(99),SM-A and bcl-2,negative for S-100,CK and desmin.Conclusions Solitary fibrous tumor of the prostate is a rare tumor.Its diagnosis depends on histopathologic and immunohistochemical studies. Radical prostatectomy and TURP are main treatment options with good prognosis.

目的探讨前列腺孤立性纤维瘤的诊断和治疗。方法总结2例前列腺孤立性纤维瘤患者资料。例140岁,表现为进行性排尿困难,会阴部胀痛不适,B超示前列腺增大,周边整齐。血清PSA 1.92 ng/ml,尿流率呈下尿路梗阻尿流曲线。例256岁,主要症状为进行性尿频、尿急、夜尿增多,B超、CT提示前列腺不均匀增大,前列腺穿刺活检确诊后,患者拒绝手术转放射治疗后失访。结合文献复习讨论。结果例1行经尿道前列腺电切(TURP),切除前列腺组织83 g,随访8个月,未见肿瘤复发,排尿通畅。例2失访。病理检查,2例肿瘤均由梭形细胞和胶原束构成,镜下见特征性黏液样变和血管外皮瘤样变。例1有丝分裂相为1个/10 HP,免疫组化:CD_(34)(+),CD_(99)(+),bcl- 2(+),S-100(-),SM-A(-)。病理诊断:前列腺孤立性纤维瘤。例2有丝分裂相为4个/10 HP。免疫组化:CD_(34)(+),CD_(99)(+),bel2(+),CK(-),S-100(-),SM-A(灶性+),desmin(-)。病理诊断:前列腺孤立性纤维瘤(恶性)。结论前列腺孤立性纤维瘤...

目的探讨前列腺孤立性纤维瘤的诊断和治疗。方法总结2例前列腺孤立性纤维瘤患者资料。例140岁,表现为进行性排尿困难,会阴部胀痛不适,B超示前列腺增大,周边整齐。血清PSA 1.92 ng/ml,尿流率呈下尿路梗阻尿流曲线。例256岁,主要症状为进行性尿频、尿急、夜尿增多,B超、CT提示前列腺不均匀增大,前列腺穿刺活检确诊后,患者拒绝手术转放射治疗后失访。结合文献复习讨论。结果例1行经尿道前列腺电切(TURP),切除前列腺组织83 g,随访8个月,未见肿瘤复发,排尿通畅。例2失访。病理检查,2例肿瘤均由梭形细胞和胶原束构成,镜下见特征性黏液样变和血管外皮瘤样变。例1有丝分裂相为1个/10 HP,免疫组化:CD_(34)(+),CD_(99)(+),bcl- 2(+),S-100(-),SM-A(-)。病理诊断:前列腺孤立性纤维瘤。例2有丝分裂相为4个/10 HP。免疫组化:CD_(34)(+),CD_(99)(+),bel2(+),CK(-),S-100(-),SM-A(灶性+),desmin(-)。病理诊断:前列腺孤立性纤维瘤(恶性)。结论前列腺孤立性纤维瘤是一种罕见肿瘤,确诊依赖病理学及免疫组织化学检查。主要治疗方式是TURP和前列腺根治术,良性病变预后好。

 
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