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Nouvelle revue francaise d'hematologie; blood cells最新文献

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[Congenital dyserythropoiesis: an unclassifiable case?]. 先天性红细胞增生症:一例无法分类的病例。
C Dao, P L Bras, M Reynes, G Bilski-Pasquier
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引用次数: 0
[Acquired idiopathic sideroblastic anemia: three cases with the same supplemental chromosome marker (47 Mar+)]. [获得性特发性铁母细胞性贫血:3例补充染色体标记相同(47 Mar+)]。
J F Dor, J F Mattéi, M G Mattéi, F Giraud, M Mongin
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引用次数: 0
[Sideroblastic anemia secondary to or associated with immunosuppression]. [继发于免疫抑制或与免疫抑制相关的铁母细胞性贫血]。
M L Porrier, J C Piette, N Kharchi, G Vaugier, P Godeau
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引用次数: 0
[Erythrocyte form and deformability for normal blood and some hereditary hemolytic anemias (author's transl)]. [正常血液和某些遗传性溶血性贫血的红细胞形态和变形能力(作者译)]。
M Bessis

1. A brief review of recent results on the structure of erythrocyte membranes and the experimental deformation of red blood cells. 2. A discussion of factors playing a role in the deformability: a) Influence of shape, consisting of the cell surface to volume ration. b) Internal factors, depending mainly on the viscosity of the hemoglobin).c) Degree of flexibility of the membrane. 3. A brief summary of techniques to measure the deformability with emphasis on the method of viscodiffractometry (ektacytometer). 4. Results given by examination in the ektacytometer of hereditary spherocytosis and sickle cell anemia.

1. 简要回顾近年来关于红细胞膜结构和红细胞实验变形的研究结果。2. 讨论了对可变形性起作用的因素:A)形状的影响,包括细胞表面与体积比。b)内部因素,主要取决于血红蛋白的粘度。c)膜的柔韧性程度。3.简要介绍了可变形性的测量技术,重点介绍了粘度衍射法(ektacyometer)。4. 遗传性球形红细胞增多症和镰状细胞性贫血的细胞计数仪检查结果。
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引用次数: 0
[Lymphography in chronic lymphocytic leukemia (author's transl)]. 慢性淋巴细胞白血病的淋巴造影术(作者简介)。
J L Binet, M G Nizet, G Dighiero, J Grellet

Sixty-seven lymphangiograms were performed in 58 patients with chronic lymphocytic leukemia. These patients were classified according to a new anatomico-clinical staging system which has previously been shown to bear prognostic significance. The lymphangiograms were divided into four groups on the basis of lymph node size and each group was further divided into subgroups (12). Each subgroup corresponded to a different roentgenographic picture. A good correlation was observed between lymphangiographic and anatomico-clinical staging: lymphangiogram groups 3 and 4, anatomico-clinical stage III and IV (p less than 0.001). The absence of normal lymph nodes in all patients, the diversity of lymphangiographic appearance from one patient to another and even the diversity from one region to another in the same patient should be stressed.

本文对58例慢性淋巴细胞白血病患者进行了67次淋巴管造影检查。这些患者根据一种新的解剖-临床分期系统进行分类,该系统先前已被证明具有预后意义。根据淋巴结大小将淋巴管造影分为四组,每组又分为亚组(12)。每个亚组对应不同的x线图像。淋巴管造影与解剖-临床分期之间存在良好的相关性:淋巴管造影组3和4,解剖-临床分期III和IV (p < 0.001)。所有患者均未见正常淋巴结,不同患者之间的淋巴管造影表现的多样性,甚至同一患者不同区域的多样性都应得到重视。
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引用次数: 0
[Chemotherapy-radiotherapy association in the treatment of localized forms of Hodgkin's disease. Prognosis of polychemotherapy after three trials of M.O.P.P]. 化疗-放疗联合治疗局限性何杰金氏病。M.O.P.P三次化疗后的预后[j]。
F Baillet, B Brun, J J Mazeron, H Rochant, G Pinon, F Reyes, J P Vernant, B Pierquin, B Dreyfus

63 patients with Hodgkin disease of limited extent (I, II, III) are treated with two protocols: extended field irradiation versus chemotherapy (M.O.P.P.) + extended field irradiation. Three points are suggested by analysis of the results: 1) Advantage from the combination of chemotherapy-radiotherapy. 2) Resistance to chemotherapy frequent innodular sclerosis. 3) In patients treated with chemotherapy the reaction has a prognostic value: failure of treatment being seen only in patients who did not obtain a complete remission.

63例有限范围(I, II, III)霍奇金病患者采用两种方案进行治疗:扩展野照射vs化疗(M.O.P.P.) +扩展野照射。通过对结果的分析,提出三点:1)放化疗联合治疗的优势。2)化疗耐药多发结节性硬化。3)在接受化疗的患者中,该反应具有预后价值:治疗失败仅见于未获得完全缓解的患者。
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引用次数: 0
[Treatment of acute leukemia]. [治疗急性白血病]。
C Jacquillat, M Weil, M F Auclerc, G Schaison, J F Holland

Evaluations of 650 patients with acute lymphoblastic leukemias (A.L.L.) and of 596 patients with acute granulocytic leukemias (A.G.L.) ara analyzed. The patients were treated in the department of Professeur Jean Bernard at Saint-Louis Hospital between 1964 and 1976. In A.L.L., prognosis is influenced primarely by age, being worse in infants less than 1 year old and in adults: it is also influenced by the blastic load and by other parameters such as cytology and immunological markers which could not be studied in all patients. The correlation between high blastic load and the T lymphoblasts variety is noteworthy. Random studies are still necessary to find out the best drug combinations and the optimal duration of treatment, but the necessity for meningeal prophylaxis, reinduction treatments and of L-A sparaginase consolidation is no longer discussed. Prognostic stratification is useful for therapeutical evaluation and should load to therapeutical modulation. In acute granulocytic leukemias, age is also a significant parameter and remission rate is lower for patients over 50 years of age. Cytology and cytochemistry allow to recognize acute promyelocytic leukemias and acute monoblastic leukemias which bear specific initial risks (D.I.C. for A.P.L., renal failure for acute monoblastic leukemia) but which are highly sensitive to Daunorubicin and Rubidazone respectively. In A.M.L. remission duration is not influenced by age and seems to be improved by intermittent treatment. The role of immunotherapy is still under study.

本文对650例急性淋巴细胞白血病(a.l.l)和596例急性粒细胞白血病(a.g.l)进行了评价分析。这些病人在1964年至1976年期间在圣路易医院让·伯纳德教授的科室接受治疗。在急性淋巴细胞白血病中,预后主要受年龄的影响,小于1岁的婴儿和成人的预后更差,还受母细胞负荷和其他参数(如细胞学和免疫学标记物)的影响,这些参数无法在所有患者中进行研究。高胚负荷与T淋巴细胞多样性之间的相关性值得注意。随机研究仍有必要找出最佳的药物组合和最佳的治疗时间,但脑膜预防、再诱导治疗和L-A sparaginase固结的必要性已不再讨论。预后分层对治疗评估是有用的,并应纳入治疗调节。在急性粒细胞白血病中,年龄也是一个重要的参数,50岁以上患者的缓解率较低。细胞学和细胞化学允许识别急性早幼粒细胞白血病和急性单核细胞白血病,它们具有特定的初始风险(A.P.L的D.I.C.,急性单核细胞白血病的肾功能衰竭),但分别对柔红霉素和鲁比酮高度敏感。急性粒细胞性白血病的缓解时间不受年龄的影响,似乎可以通过间歇性治疗得到改善。免疫疗法的作用仍在研究中。
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引用次数: 0
[Combined immunological and cytochemical identification of nucleated cells in normal human peripheral blood]. 正常人外周血有核细胞的免疫学和细胞化学联合鉴定。
A Alario, A L Claudy, M Faure, J Thivolet

Nucleated cells obtained from normal human peripheral blood on a layer of Ficoll Isopaque are identified according to the combination of various assays: phagocytosis, endogenous peroxidase, naphtol AS-D esterase, immunofluorescence (IF) performed at 4 degrees C and after incubation at 37 degrees C. The Ig bearing lymphocytes are evaluated with IF, while errors due to other nucleated cells may be evaluated by phagocytic and enzymatic capacities. As the presence of immunoglobulins (Ig) on the cell surface doses not prove its B lymphocytic nature, both immunofluorescence (IF) and endogenous peroxidase are usefully performed together. Exposure of the cells to 37 degrees C during half an hour may enable us to avoid to consider monocytes and lymphocytes with cell bound Ig. Thus con accurately be evaluated the percentages of lymphocytic populations in practice of immunological tests.

从正常人外周血中获得的有核细胞在Ficoll Isopaque层上进行鉴定,根据多种检测方法的组合进行鉴定:吞噬、内源性过氧化物酶、萘酚AS-D酯酶、免疫荧光(IF),在4℃和37℃孵卵后进行。携带Ig的淋巴细胞用IF评估,而其他有核细胞的错误可能通过吞噬和酶促能力来评估。由于免疫球蛋白(Ig)在细胞表面的存在剂量不能证明其B淋巴细胞性质,因此免疫荧光(IF)和内源性过氧化物酶可以同时进行。将细胞暴露于37℃半小时可使我们避免考虑单核细胞和淋巴细胞结合Ig。因此,在实际的免疫试验中,可以准确地评估淋巴细胞群体的百分比。
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引用次数: 0
[Hematologic disorders observed in patients following renal transplantation]. [肾移植术后患者血液系统疾病的观察]。
A M Fischer, A Cosson, T Drueke, C Barbanel, F Josso
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引用次数: 0
[Scintigraphy with indium 111 in hematosarcoma]. [111铟在血液肉瘤中的显像]。
J Fretault, G Bilski-Pasquier
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引用次数: 0
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Nouvelle revue francaise d'hematologie; blood cells
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