全血细胞减少
- pancytopenia
-
结论低危MDS患儿多为学龄期儿童,全血细胞减少最多见。
Conclusions The patients of low-risk MDS are mostly school-aged children and pancytopenia is the most common sign .
-
以全血细胞减少为首发表现的急性白血病临床分析
Clinical analysis of acute leukemia with pancytopenia as the first-onset manifestation
-
Bayes判别分析全血细胞减少的分类诊断
Application of Bayes discriminatory analysis in the classification of pancytopenia
-
10例患者全血细胞减少,全部患者均具有典型的巨幼贫骨髓象,血清中叶酸或维生素B_(12)定量减少。
Ten cases showed pancytopenias . All patients presented typical morphologic manifestations of megaloblastic marrow with small megakaryocytes and low serum vitamin B12 and folic acid levels .
-
目的:再生障碍性贫血(AA)是一种T细胞免疫相关的疾病,其特征是全血细胞减少和骨髓发育不良。
Objective : Aplastic anemia behaves as an immune-mediated disease characterized by pancytopenia and hypoplastic bone marrow .
-
目的了解与免疫相关全血细胞减少患者骨髓造血祖细胞增殖分化功能以及辅助性T(Th)淋巴细胞在此类患者发病中的作用。
Objectives To explore the proliferative capacity of bone marrow hematopoietic stem cells and the function of T helper ( Th ) lymphocytes of patients with immuno-related pancytopenia ( IRP ) .
-
方法对我院住院的急性白血病患者和全血细胞减少症病人同步进行骨髓活检与涂片检查,骨髓活检标本经处理后,塑料包埋,切成3μm切片,HGF染色。
Methods We study simultaneously bone marrow smear and trephine biopsy in 71 patients with pancytopenia and 34 patients with acute leukemia .
-
目的探讨免疫相关性全血细胞减少症(IRP)患者骨髓中辅助性T淋巴细胞(Th)亚群数量、功能改变及在发病中的作用。
Objective To explore the subsets and function of T helper ( Th ) cells in bone marrow of the patients with immune-related pancytopenia ( IRP ) .
-
毛细胞白血病(HCL)以全血细胞减少和巨脾为特征,CD11C、CD25和超微结构对其诊断有极大帮助;
A low blood cell count and splenomegaly were usually seen in HCL . CD11c + , CD25 + and ultrastructural analysis were useful for the diagnosis .
-
目的提高对儿童急性淋巴细胞白血病前期(Pre-ALL)全血细胞减少的认识。
Objective To report the development of children transient pancytopenia preceding acute lymphoblastic leukemia ( Pre-ALL ) .
-
我们提出的抗体组合适用于鉴别诊断RCMD和AA及其他全血细胞减少疾病,但还需要进一步的前瞻性研究来评价。
The new antibodies combination we proposed is used for the differential diagnosis between RCMD and AA or other pancytopenia diseases , but it should be evaluated in the further prospective researchs .
-
方法报道1例伴有t(11;14)(q10;q10)易位的T细胞型Pre-ALL全血细胞减少患儿的临床特征及诊治经过,并进行文献复习。
Methods A case of Pre-ALL characterized by T cell immunophenotype and abnormal karyotype t ( 11 ; 14 )( q10 ; q10 ) is discussed with review of literatures .
-
全血细胞减少的巨幼细胞性贫血15例临床分析
The clinical analysis of 15 patients with megaloblastic anemia with pancytopenia
-
小剂量阿司匹林肠溶片致全血细胞减少
Low - dose aspirin enteric - coated tablet resulting in panhematopenia
-
骨髓活检同步观察在全血细胞减少症中的诊断价值
Diagnosis value of synchronism marrow biopsy and bone marrow smear on pancytopenia
-
实验室显示全血细胞减少、血清酶学显著增高。
Laboratory examinations revealed pancytopenia , and remarkably higher serum enzymes levels .
-
环孢素A选择性治疗10例全血细胞减少患者的临床研究
Clinical Study on 10 Cases of Pancytopenia Selectively Treated by Cyclosporine A
-
全血细胞减少718例细胞形态学分析
Analysis of cell morphology for 718 cases of panhematopenia
-
全血细胞减少的鉴别诊断&68例病历分析
Differential Diagnosis of Pancytopenia : Analysis of 68 Cases
-
对象:纳入107例初诊的全血细胞减少患者。
PARTICIPANTS : A total of107 pancytopenia patients following first diagnosis were enrolled .
-
全血细胞减少125例病因分析
Analysis of Causes of Cytopenia in 125 patients
-
儿童急性杂合性白血病前期全血细胞减少1例报告并文献复习
Children transient pancytopenia preceding hybrid acute leukemia : One case report and review of literature
-
结论:对于非血液系统疾病引起的全血细胞减少,临床医师应予以足够重视。
Conclusion : Clinicians should attach great importance to cytopenia caused by non-blood systemic diseases .
-
肺结核患者全血细胞减少的发病机理探讨
Pancytopenia in patients with pulmonary tuberculosis
-
目的:构建全血细胞减少分类诊断的判别函数。
OBJECTIVE : To construct a mechanism model for the diagnosis of pancytopenia by discriminatory analysis .
-
小儿全血细胞减少相关疾病
Children ' Diseases Related to Pancytopenia
-
免疫相关全血细胞减少患者骨髓造血祖细胞增殖功能及辅助性T淋巴细胞功能观察
Proliferation of bone marrow hematopoietic stem cells and function of T helper lymphocytes of patients with immuno-related pancytopenia
-
目的探讨骨髓组织活检在全血细胞减少症中的临床作用。
Objective To explore the clinical effect of bone marrow biopsy on differential diagnosis for patients with pancytopenia .
-
都患有全血细胞减少伴皮肤色素沉着,拇指缺如,生殖器发育不良等先天性畸形。
Their characterlstic associated abnormalities include peripheral pancytopenia , hyperpigmentation , deformity of the thumbs and genital hypoplasia .
-
骨髓检查在全血细胞减少中的诊断价值及320例病因分析
Evaluation of Bone Marrow Examinations in Differential Diagnosis for Patients with Pancytopenia and Causal Analysis of 320 cases