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plasmacyte type
相关语句
  浆细胞型
     M/F ratio was 1.8∶1 According to histopathologic subclassification, 23 cases are organized pneumonia type, 16 cases were fibrous tissue type and 11 cases were lymphocyte plasmacyte type.
     结果 :机化肺炎型 2 3例 ,纤维组织细胞型 1 6例 ,淋巴浆细胞型 1 1例 ;
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  “plasmacyte type”译为未确定词的双语例句
     Methods: There are five cases of MCD, and three of them are plasmacyte type (PC) , two of them are hyaline vessel type (HV). Five cases are all male and the age from 43 to 62 year old.
     方法:MCD患者5例,其中浆细胞型(PC)3例,透明血管型(HV)2例,均为男性,年龄43岁~62岁(中位年龄50岁)。
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  相似匹配句对
     Type of Y.
     针对 Y.
短句来源
     illiensis type and T.
     iliensis type、T.
短句来源
     Plasmacyte in pseudotumor came fromlymphocytic cel differentiation.
     经检测炎性假瘤中的浆细胞可能多数来自淋巴细胞 ;
短句来源
     The Rare Side Effects of Thalidomide in Treating Malignant Plasmacyte Disease
     反应停治疗恶性浆细胞疾病时的罕见不良反应
短句来源
     5 of 16 cases had local inflammation infiltration with lymphocyte and plasmacyte.
     有5/16的病例局部有以淋巴细胞和浆细胞为主的炎性浸润。
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Objective:To investigate the clinical pathologic feature of inflammatory pseudotumor in the lung.Methods:50 cases of inflammatory pseudotumor in the lung were studied by clinical pathology according to pathological types invented by HUN PATHOL and MATSUBRA in 1988.Results:32 male and 18 female, age ranged 17~69 years (average age 43) were included in this study. M/F ratio was 1.8∶1 According to histopathologic subclassification, 23 cases are organized pneumonia type, 16 cases were fibrous tissue type and 11...

Objective:To investigate the clinical pathologic feature of inflammatory pseudotumor in the lung.Methods:50 cases of inflammatory pseudotumor in the lung were studied by clinical pathology according to pathological types invented by HUN PATHOL and MATSUBRA in 1988.Results:32 male and 18 female, age ranged 17~69 years (average age 43) were included in this study. M/F ratio was 1.8∶1 According to histopathologic subclassification, 23 cases are organized pneumonia type, 16 cases were fibrous tissue type and 11 cases were lymphocyte plasmacyte type.Conclusion:The all inflammatory pseudotumors in the lung are the benign tumor and male is more than female. The pathological features show that the fibroblasts hyperplasia, the blood vessel hyperplasia, the histocylymphocytes and plasmacyte infiltrate and pulmonary alveolus cell proliferate.

目的 :探讨肺炎性假瘤的病理类型和临床特点 ;方法 :根据 1 988年 (HUNPATHOL)MATSUBRA等分型方法 ,对 50例肺炎性假瘤进行临床病理分析 ;结果 :机化肺炎型 2 3例 ,纤维组织细胞型 1 6例 ,淋巴浆细胞型 1 1例 ;结论 :肺炎性假瘤其性质均为良性 ,男性多于女性 ,共同的病理特点是纤维母细胞增生、血管增生 ,组织细胞、淋巴细胞、浆细胞浸润 ,肺泡细胞增殖

Objective: To analyze the clinical manifestations and pathological feature of multicenter Castleman disease (MCD). Methods: There are five cases of MCD, and three of them are plasmacyte type (PC) , two of them are hyaline vessel type (HV). Five cases are all male and the age from 43 to 62 year old. Four cases of MCD accept chemotherapy including COP, and they maintain therapy with glucocorticoid or thalidomide plus interferon. One patient give up treatment. Results: Clinical stat: five patients...

Objective: To analyze the clinical manifestations and pathological feature of multicenter Castleman disease (MCD). Methods: There are five cases of MCD, and three of them are plasmacyte type (PC) , two of them are hyaline vessel type (HV). Five cases are all male and the age from 43 to 62 year old. Four cases of MCD accept chemotherapy including COP, and they maintain therapy with glucocorticoid or thalidomide plus interferon. One patient give up treatment. Results: Clinical stat: five patients is characterized by different fever, faint and night sweats etc. aspecific clinical symtom. And the five cases all have lymphadenopathy, as well as three of them have be found splenomegaly. Laboratory result: there are three patients are found to be anaemia and renal function lesion. Four patients presented hypergammaglobulinemia . In the bone marrow, there four cases show plasmocyte increasing or eosinophilia. Therapeutic efficacy: one case free survive eight years after COP four courses; two patients achieved partly remission after chemotherapy and still be following-up. Conclusion: MCD is usually characterized by polysystem damage in clinical manifestations with enlarged lymph nodes. If systemic manifestations occur earlier than lymphadenopathy, it is difficulty to diagnose MCD. This disorder must be proved by lymph node biopsied.

目的:分析多中心Castleman病(MCD)的临床病理特点。方法:MCD患者5例,其中浆细胞型(PC)3例,透明血管型(HV)2例,均为男性,年龄43岁~62岁(中位年龄50岁)。4例接受COP化疗,并分别应用糖皮质激素、沙利度胺+干扰素维持,1例放弃治疗。结果:临床情况5例分别不同程度表现发热、乏力、盗汗等非特异性全身症状,5例均存在多部位浅表淋巴结肿大,3例脾脏肿大。实验室结果:出现贫血及肾功能损害各有3例,4例患者出现多克隆高γ球蛋白血症,4例患者骨髓浆细胞或嗜酸粒细胞增多。治疗转归:1例4疗程COP治疗后生存8 a,2例治疗后达PR,带病生存4个月、8个月,仍随访中。结论:多中心CD常累及多系统损伤,且表现较淋巴结肿大为早,PC型全身症状相对较重,致使MCD早期诊断存在困难,确诊须经淋巴结病理活检证实。

 
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