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   淋巴细胞为主型 的翻译结果: 查询用时:0.791秒
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淋巴细胞为主型
相关语句
  lymphocyte-predominant
     Differential diagnosis between nodular lymphocyte-predominant Hodgkin lymphoma and T-cell/ histiocyte-rich B-cell lymphoma
     结节性淋巴细胞为主型霍奇金淋巴瘤和富于T细胞和(或)组织细胞的B细胞淋巴瘤的鉴别诊断
短句来源
     Objective To study the differential diagnosis between nodular lymphocyte-predominant Hodgkin lymphoma (NLPHL) and T-cell/histiocyte-rich B-cell lymphoma (TCRBCL).
     目的探讨结节性淋巴细胞为主型霍奇金淋巴瘤(NLPHL)和富于T细胞和(或)组织细胞的B细胞淋巴瘤(TCRBCL)的鉴别诊断。
短句来源
     Diagnosis and differential diagnosis of nodular lymphocyte-predominant Hodgkin′s lymphoma
     结节性淋巴细胞为主型霍奇金淋巴瘤的诊断与鉴别诊断
短句来源
     Among them, lymphocyte-predominant (LP), nodular scler-otic (NS), mixed cellular (MC) and lymphocyte-depletion types are acco-
     以淋巴细胞为主型(LP型)者多为临床Ⅰ~Ⅱ期,结节硬化型(NS型)者多为Ⅱ~Ⅲ期,淋巴细胞消减型(LD型)者多为Ⅳ期,混合细胞型(MC型者)则介于Ⅰ~Ⅳ之间; LP型以累及单一浅部淋巴结为主,LD、MC及NS型常累及内脏;
短句来源
     The expression rates of Oct2 protein in nodular lymphocyte-predominant Hodgkin lymphoma and classic Hodgkin lymphoma were 3/3 and 46.2% (6/13) respectively. The difference in expression rates of Oct2 protein in these two groups showed no statistical significance (P>0.05).
     在结节性淋巴细胞为主型霍奇金淋巴瘤(NLPHL)和经典型霍奇金淋巴瘤(CHL)分别为3例均阳性和46.2%(6/13),后两组间比较P>0.05。
短句来源
  lymphocyte predominant
     According to its characteristic histology, HL is devided into two main types in update WHO Classification of Tumors: nodular lymphocyte predominant HL (NLPHL) and classical HL (CHL).
     在最新WHO疾病分类中,根据其组织学特征分为结节性淋巴细胞为主型(nodular lymphocyte predominant HL,NLPHL)和经典型(classical HL,CHL)2种类型。
短句来源
     Advances in lymphocyte predominant Hodgkin's disease
     淋巴细胞为主型霍奇金病的研究进展
短句来源
     Results Apoptosis (TUNEL) rates of RS/H cells in lymphocyte predominant (LP) and nodular sclerosing (NS) subtypes were remarkably higher than that in mixed cellular (MC) and lymphocyte depleted (LD) subtypes( P< 0 005). Positive rates of PCNA in RS/H cells of LP and NS subtypes were slightly higher than that of MC and LD subtypes.
     结果:淋巴细胞为主型和结节硬化型HD的RS/H细胞凋亡发生率明显高于混合细胞型和淋巴细胞消减型者(P<0005),PCNA阳性率前者仅略高于后者;
短句来源
     Objective To study the diagnosis and the differential diagnosis of nodular lymphocyte predominant Hodgkin′s lymphoma (NLPHL).
     目的 探讨结节性淋巴细胞为主型霍奇金淋巴瘤 (NLPHL)的诊断和鉴别诊断特点。
短句来源
     Lymphocyte predominant Hodgkin's disease (LPHD) or nodular lymphocyte predominant Hodgkin's disease (NLPHD) is a rare type of B-cell lymphoma with a unique pathologic and clinical features that distinguish it from classical Hodgkin's disease (CHD).
     淋巴细胞为主型霍奇金病(LPHD)或结节性淋巴细胞为主型霍奇金病(NLPHD)不同于结节硬化型、混合细胞型等经典型霍奇金病(CPHD),是一种少见的、具有独特的病理和临床特征的B细胞淋巴瘤。
短句来源
  “淋巴细胞为主型”译为未确定词的双语例句
     Methods:Morphologic studies and immunohistochemical analyses of BCL-6, CD10 and BCL-2 protein expression were performed on 135 cases of B-NHL frequently occurred in Chinese populations and 5 cases of T-NHL, 5 cases of nodular lymphocyte predominance Hodgkin’s lymphoma (NLPHL) and 10 cases of reactive hyperplasia of lymph node (LRH) with paraffin-embedded tissues.
     方法:对135例中国人常见类型的B-NHL和对照组5例T-NHL、5例结节型淋巴细胞为主型霍奇金淋巴瘤(Nodular lymphocyte predominance Hodgkin’s lymphoma,NLPHL)以及10例淋巴结反应性增生(Lymphoid reactive hyperplasia,LRH)石蜡包埋组织进行形态学观察和BCL-6、CD10以及BCL-2等抗体的免疫组织化学染色;
短句来源
     Results (1) IgH and Vκ4 rearrangements were repeatedly found in H/RS cells from one case of lymphocytic predominant HD (LPHD).
     结果1例淋巴细胞为主型(LP)HD的H/RS细胞重复出现IgH和Vκ4家族重排;
短句来源
     The subtypes of HD were nodular sclerosis in 5 cases, mixed cellular in 3 cases, lymphocytic predominance in 1 case.
     病理亚型为结节硬化型5例,混合细胞型3例,淋巴细胞为主型1例。
短句来源
     The results are as follows:firstly, most. of the R-S cells of non-LPHD reacted with LeuM1 (64.3%) but not with LCA, L26, and UCHL1;
     结果:非淋巴细胞为主型何杰金病(nonLPHD)的R-S细胞对LeuM_1的阳性率为64.3%,对LCA、L_(26)和UCHL_1呈阴性反应;
短句来源
     SCL and CZR were significantly higher in the patients with lymphocyte depleted type(LD)than mixed cellulal type(MC), SCL and CZR were higher in MC type than nodular sclerosis type(NS)and lymphocyte predominance type (LP)( P<0 01 ).
     同时在HD患者中 ,淋巴细胞消减型 (LD)患者组SCL和CZR明显高于混合细胞型 (MC)组 ,而MC组则显著高于结节硬化型 (NS) ,NS组又显著高于淋巴细胞为主型 (LP) ,均P <0 0 1。
短句来源
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  lymphocyte-predominant
Lymphocyte-predominant Hodgkin's lymphoma (LPHL) differs in histologic and clinical presentation from classical Hodgkin's lymphoma (cHL).
      
Rituximab for lymphocyte-predominant Hodgkin's disease
      
Strong nuclear positivity forbcl-6 was consistently detected in tumor (L >amp;amp; H) cells of nodular, lymphocyte-predominant Hodgkin's disease (NLPHD).
      
Strong nuclear positivity forbcl-6 was consistently detected in tumor (L >amp;amp; H) cells of nodular,lymphocyte-predominant Hodgkin's disease (NLPHD).
      
Cells from five cases of HD [four classic HD and one lymphocyte-predominant (LP) HD] were examined by single-cell analysis for the T-cell receptor (TCR) γ gene.
      
更多          
  lymphocyte predominant
Lymphocyte predominant Hodgkin's disease (LPHD) is a rare type of B-cell lymphoma with unique pathologic and clinical features that distinguish it from other types of Hodgkin's disease.
      
HRS cells in classical HD as well as lymphocyte predominant (LP) HD originate from germinal center (GC) B cells in most cases, if not all.
      
Lymphocyte predominant Hodgkin's disease: Pathology and clinical implication
      
Patients with lymphocyte predominant (LP) HD, predominantly male and 25-45 years old, usually present with early clinical stage, cervical or inguinal involvement and few if any adverse prognostic factors.
      
Lymphocyte predominant Hodgkin's disease of nodular subtype combined with pulmonary lymphoid infiltration and hypogammaglobulina
      
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33 cases of Hodgkin's disease in children are reviewed and analyzed in this paper. Among them, lymphocyte-predominant (LP), nodular scler-otic (NS), mixed cellular (MC) and lymphocyte-depletion types are acco-

33例小儿何杰金氏病(HD)发病年龄高峰为5—9岁,男女之比为4.5:1;以淋巴细胞为主型(LP型)者多为临床Ⅰ~Ⅱ期,结节硬化型(NS型)者多为Ⅱ~Ⅲ期,淋巴细胞消减型(LD型)者多为Ⅳ期,混合细胞型(MC型者)则介于Ⅰ~Ⅳ之间;LP型以累及单一浅部淋巴结为主,LD、MC及NS型常累及内脏;颈部淋巴结为最常见的发病部位。半年以内死亡率:LP型为10%,NS型为11%,MC型为14%,LD型为100%。未经治疗或经单一化疗或放疗者预后差,半年内死亡率为58%;放疗加化疗综合性治疗,预后较好,三年以上存活率为69%。

A pathological study of 124 cases with thymomas was reviewed. These thymomas were diveded into predominantly lymphocytic(39), predomonantly epithelial(40), mixed(46).The most significant prognostic features of the thymomas was the presence or absence of gross invasion of adjacent or capsule. 37 of tumors were invasive thymomas, 87 were noninvasive. The thymomas of 51 cases were detected by chest Ⅹ-ray. Myasthenia gravis was present in 22 cases. One had red cell hypoplasia. This syndrome was discussed in the...

A pathological study of 124 cases with thymomas was reviewed. These thymomas were diveded into predominantly lymphocytic(39), predomonantly epithelial(40), mixed(46).The most significant prognostic features of the thymomas was the presence or absence of gross invasion of adjacent or capsule. 37 of tumors were invasive thymomas, 87 were noninvasive. The thymomas of 51 cases were detected by chest Ⅹ-ray. Myasthenia gravis was present in 22 cases. One had red cell hypoplasia. This syndrome was discussed in the paper.

本文对124例胸腺瘤的病理形态作了详细描述,根据其包膜有否浸润及转移,将肿瘤分为良性87例,恶性37例。按组织学形态将肿瘤分为淋巴细胞为主型39例,上皮细胞为主型45例,混合型40例。本文尚对胸腺瘤的有关临床表现如重症肌无力单纯红细胞性贫血等进行了讨论。

The morphologic features of L/H type R-S cells by light and electron microscopy, enzyme histochemistry and immunphistochemistry of 20 HD patients of lym-phocytic predominant type was studied . The results showed that the L/H R-S cell size is about 12-50 μm with mono nucleus or multinuclei. The former one was characterized by a folded , complex, convoluted nuclear envelope. The latter one had multiple forms of nuclei such as circular, horseshoelike, osteoclast-like, and so on. The nucleolus was small and basophilic....

The morphologic features of L/H type R-S cells by light and electron microscopy, enzyme histochemistry and immunphistochemistry of 20 HD patients of lym-phocytic predominant type was studied . The results showed that the L/H R-S cell size is about 12-50 μm with mono nucleus or multinuclei. The former one was characterized by a folded , complex, convoluted nuclear envelope. The latter one had multiple forms of nuclei such as circular, horseshoelike, osteoclast-like, and so on. The nucleolus was small and basophilic. With ANAE and ACP staining they were slight to morderate positive in Cytoplasm. The IgG was polydonal. The Leu-Mi mark was positive in 3/11 cases.The L/H.type R-S cells were.distributed in the background of lymphocytes and histocy-tes. The poly polar mitosis .was seen frequently. It was probably a precursor of other R-S cells. It was emphasized that lymphocytic predominant type HD must be differentiated from early malignant histocytbsis, metastatic undifferentiated carcinoma and immunoblastic lymphoadenopathy.

对20例淋巴细胞为主型何杰金氏病组织切片应用HE、酶组化免疫组化及电镜等方法观察了L/H型R—S细胞的形态学特征。观察结果提示:L/H型R—S细胞体积大(12.5~50μm),以单核为主,核膜褶叠扭曲。少数多核或多叶核,有排成马蹄形、花环形或破骨细胞样等形式。核仁小而嗜喊。同时常伴有固缩型R—S细胞及瘤型分裂像。部份病例可找到个别诊断型R—S细胞。对本型R—S细胞的生物学意义,诊断与鉴别诊断进行了讨论。

 
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