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血管免疫母细胞
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  angio-immunoblastic
     NATURE OF ANGIO-IMMUNOBLASTIC LYMPHADENOPATHY
     血管免疫母细胞性淋巴结病病变性质的研究
短句来源
     Angio-immunoblastic lymphadenopathy:case report
     血管免疫母细胞淋巴结病1例
短句来源
     Objective To analyze the etiology and the clinical features of angio-immunoblastic lymph-adenopathy were discussed.
     目的 :探讨血管免疫母细胞性淋巴结病 (AIL D)发病因素和临床特征。
短句来源
  angioimmunoblastic
     THE EXPRESSION OF bcl-2 AND P53 PROTEINS IN ANGIOIMMUNOBLASTIC LYMPHADENOPATHY
     血管免疫母细胞性淋巴结病bcl-2与P53蛋白表达
短句来源
     THE EXPRESSION OF P53 PROTEIN AND DNA CONTENT ANALYSIS IN ANGIOIMMUNOBLASTIC
     血管免疫母细胞性淋巴结病P53蛋白表达及DNA含量分析
短句来源
     Angioimmunoblastic T cell lymphoma 14 cases clinical analysis
     血管免疫母细胞性T细胞淋巴瘤14例临床分析
短句来源
     Clinical Analysis of Angioimmunoblastic T-cell Lymphoma in Children
     儿童血管免疫母细胞性T细胞淋巴瘤临床分析
短句来源
     Gene rearrangement and p53 expression in defining the nature of angioimmunoblastic lymphadenopathy
     基因重排分析与p53的表达在判定血管免疫母细胞性淋巴结病性质上的意义
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  “血管免疫母细胞”译为未确定词的双语例句
     Results Dill'use large B-cell lymphoma(DLBCL)constituted 38.1% of the cases followed by follicular lymphoma(FL) 17.4% ,small lymphocytic lymphoma(SLL) 10.3% ,peripheral T-cell lymphoma(PTCL)(unspecified) 8.4% ,and angioimmunnblastic lymphoma 7.1%.
     结果 155例 NHL 患者中常见的病理类型是弥漫大 B 细胞淋巴瘤(DLBCL)(59例,38.1%)、滤泡性淋巴瘤(27例,17.4%)、B 小淋巴细胞淋巴瘤(16例,10.3%)、非特指周围 T 细胞淋巴瘤(13例.8.4%)、血管免疫母细胞性 T细胞淋巴瘤(11例,7.1%)。
短句来源
     Objective To improve the diagnosis and therapy of children angioimmunoblatic T-cell lymphoma (AITL) by analyzing the clinical parameters of AITL.
     目的 通过对 6例儿童血管免疫母细胞性T细胞淋巴瘤 (AITL)临床表现的分析 ,为儿童AITL的诊断和治疗提供依据。
短句来源
     Using fluorescence in situ hybridization, we have detected trisomy 3 and the frequency of cells with +3in 36 patients with AILD.
     运用荧光原位杂交技术,检测36例血管免疫母细胞性淋巴结病(AILD)中常见的3号染色体三体(+3)的发生率及含有+3的畸变细胞率。
短句来源
     Six nodes in 2 cases showed with vascular immunoblast lymph node lesions which appeared centric blood flow with rich branches passing regularly.
     2例血管免疫母细胞淋巴结病发现6个淋巴结,3D-CDE血流呈树枝状,分支丰富,走行规则。
短句来源
     Objective To improve the diagnosis and therapy of AILD by analysing the clinical features of AILD.
     目的 通过对血管免疫母细胞淋巴结病 (AILD)临床表现的分析 ,为 AIL D的诊断和治疗提供依据。
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  angio-immunoblastic
Histological, immunohistological and autopsy findings in lymphogranulomatosis X (including angio-immunoblastic lymphadenopathy)
      
Angio-immunoblastic T-cell lymphoma in evolution: A case report
      
Angio-immunoblastic T-cell lymphoma (AITL), a rare disease that constitutes 1% to 2% of non-Hodgkin's lymphomas, presents in middle-aged and elderly individuals.
      
  angioimmunoblastic
Treatment of a patient with a nodal peripheral T-cell lymphoma (Angioimmunoblastic T-cell lymphoma) with a human monoclonal anti
      
A patient with a CD4+ refractory peripheral T-cell lymphoma (PTL), subtype angioimmunoblastic T-cell lymphoma (AILD), was treated with a human monoclonal anti-CD4 antibody (HuMax-CD4) iv once weekly for 10 wk.
      
Treatment of angioimmunoblastic T-cell lymphoma with cyclosporine
      
The angioimmunoblastic lymphadenopathies showed strikingly high percentages of EA- and EAC-rosettes forming cells and showed a marked increase of SCMC and ADCC activities after elimination of mononuclear phagocytes from the effector cell population.
      
PAS-positive lymphatic cells in angioimmunoblastic lymphadenopathy
      
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Three cases of children angioimmunoblastic lymphadenopathy with dysproteinemia are reported. The characteristics of the disease were fever, skin rash, liver and spleen enlargement, generalized lymphadenopathy and increase of serum gamma globulin and immunoglobulin. Pathological changes of lymphnodes were characteristic. Diagnosis of the disease was confirmed by lymphnode biopsy.

本文报道3例儿童血管免疫母细胞淋巴结病。该病特征是发热、皮疹、肝脾肿大、全身性淋巴结肿大。免疫学检查显示血清γ球蛋白和免疫球蛋白升高。淋巴结病理改变是特异性的。确诊须靠淋巴结活体组织检查。本病目前无特效治疗。3例患儿于住院期间给予“CVP”(cytoxan,vincristinum,prednisonum)联合化疗,近期疗效尚好。本病预后不良。

The clinical and pathologic findings ih 14 patients with angioimmunoblastic lymphadenopathy(AILD)are presented.The patients' ages ranged from 5 to 67 yearswith a median age of 43 years. This series included 8 men and 6 women. Theclinical presentation is suggested as malignant lympboma. All of the patients hadlymphadenopathy, 10 patients had fever, 7 had hepatomegaly, 7 splenomegaly, 5severe anemia and skin rashes in two. Hypergammaglobulinemia was found in 5of 6 patients. Four patients was die of disease rapidly...

The clinical and pathologic findings ih 14 patients with angioimmunoblastic lymphadenopathy(AILD)are presented.The patients' ages ranged from 5 to 67 yearswith a median age of 43 years. This series included 8 men and 6 women. Theclinical presentation is suggested as malignant lympboma. All of the patients hadlymphadenopathy, 10 patients had fever, 7 had hepatomegaly, 7 splenomegaly, 5severe anemia and skin rashes in two. Hypergammaglobulinemia was found in 5of 6 patients. Four patients was die of disease rapidly (6 to 12 month) afterdiagnosis. Moreover, immunoblastic sarcoma was appeared in autopsy. The main fea-tures of pathology are: extensive alteration in the nodal architecture, abundantsmall vessels with hyperplasia endothelium, pronounced proliferation of immuno-blasts and pre-plasmacytes and plasmacytes with varied infiltration of acidocytes.

本文对血管免疫母细胞性淋巴结病的临床和病理所见作了介绍。年龄5~67岁,平均43岁。男性8例,女性6例,临床表现与恶性淋巴瘤相似,都有淋巴结病。发热10例,肝脏肿大7例,脾脏肿大7例,严重贫血5例及皮肤疹2例。4例分别于6~12个月死亡,1例尸检证实已发展为免疫母细胞肉瘤。病理组织学上主要表现是淋巴结的广泛破坏,丰富的小血管及内皮细胞的增生,显著的免疫母细胞、前浆及浆细胞的增生和不同程度的嗜酸性粒细胞浸润。

The pathological slices were made for the lymph nodes in 6 patients with angioimmunoblastic lymphodenopathy. In HE staining,the fundamental pathological charactoristics were remarkable microvascular proliferation,obvious iramunoblastic cells in filtration and many other kinds of immune cells infiltration accompanied by nondefinite eosinophilic substance deposition in microvessesl. In histochemical staining, PAS and Peroning were both positive. In immunohistochemical staining,IgG、IgM in immunoblast cells were...

The pathological slices were made for the lymph nodes in 6 patients with angioimmunoblastic lymphodenopathy. In HE staining,the fundamental pathological charactoristics were remarkable microvascular proliferation,obvious iramunoblastic cells in filtration and many other kinds of immune cells infiltration accompanied by nondefinite eosinophilic substance deposition in microvessesl. In histochemical staining, PAS and Peroning were both positive. In immunohistochemical staining,IgG、IgM in immunoblast cells were positive in 4 cases,Kappa and Lambda positive in 5 cases. The above findings showed that the disease (AIBL) is a kind of active immune reaction,but not real carcinoma. In 3 cases, Intracellular rubella virus antigens were positive, which indicated there was close relationship of AIBL to rubella virus.

作者对6例血管免疫母细胞淋巴结病患者的淋巴结HE染色病理切片进行观察,发现其基本病理特征为小血管显著增生,以免疫母细胞为主的多种免疫细胞浸润,伴有细胞间及小血管壁有无定型嗜酸性物质沉积。其组织化学染色PAS及派若宁均阳性。免疫组织化学染色:4例免疫母细胞内IgG、IgM阳性,5例Kappa、Lambda染色阳性。这说明本病是一种活跃的免疫反应,而不是真正的肿瘤。有3例其细胞内风疹病毒抗原阳性,表明某些血管免疫母细胞淋巴结病与风疹病毒有密切关系。

 
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