ACTA HAEMATOLOGICA POLONICA波兰血液学学报

ACTA HAEMATOLOGICA POLONICA(英文缩写 ACTA HAEMATOL POL),ISSN 0001-5814,eISSN 2300-7117,中文译名:波兰血液学学报 是一本学术期刊。本页汇总该期刊的最新影响因子、分区信息以及最新收录于 PubMed 的文献,帮助您快速了解期刊全貌。

2026 年数据 · 影响因子
0.600
JCR 分区
Q4
CAS 分区
-
近一年发文量
0
本站 PubMed 收录统计

发文量统计区间:2025-09-27 至 2026-09-27,按本站收录文献的发表日期统计。

ISSN: 0001-5814 · eISSN: 2300-7117 · 缩写: ACTA HAEMATOL POL ·中文: 波兰血液学学报

期刊介绍

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期刊简介

《Acta Haematologica Polonica》是波兰血液学会的官方期刊,主要发表血液学领域的临床与实验研究。内容涵盖血液肿瘤、贫血、凝血障碍、造血干细胞移植及输血医学等方向,读者群包括血液科医师、肿瘤科医师、实验室研究人员及相关专业医学生。该刊注重中东欧地区的临床实践与研究成果,为区域内外学者提供交流平台。

研究方向

主要研究方向包括白血病、淋巴瘤、骨髓瘤等血液肿瘤,以及红细胞疾病、血小板与凝血异常、骨髓衰竭和造血干细胞移植。论文类型涵盖原创临床研究、病例报告、综述、短篇通讯和致编辑信,也关注血液学诊断技术与治疗进展。

期刊特色

研究取向偏重临床实用性与区域流行病学特点,论文常报告单中心或多中心临床经验。原创研究要求有明确临床意义,病例报告需具独特教学价值。适合血液科临床医师、检验医学人员及关注中东欧血液学发展的研究者阅读与投稿。

投稿难度

投稿难度中等偏下,但并非仅因分区靠后而容易录用。该刊重视临床资料的完整性和区域相关性,对研究设计、统计方法和英文写作有一定要求。建议投稿前完善数据、规范伦理声明,并请同行润色语言,以提升送审与接收机会。

历年影响因子趋势

JCR 数据年份影响因子JCR 分区
20250.600Q4

ACTA HAEMATOLOGICA POLONICA 最新收录文献

  1. JCR分区: Q4 CAS分区: N/A 影响因子: 0.6

    1. {"_":" medycyno regeneracyjna?: Quo Vadis Regenerative Medicine?","i":["Quo Vadis"]}

    作者:
    Mariusz Z Ratajczak, Malwina Suszyńska
    日期:
    2013-07-01

    There are presented the most important sources of pluripotent stem cells for potential application in the regenerative medicine. This review summarizes also advantages and disadvantages for potential application of these cells in clinical medicine.

  2. JCR分区: Q4 CAS分区: N/A 影响因子: 0.6

    2. [RHnull syndrome--diagnostic and therapeutic problems].

    PMID:
    作者:
    G Kuśnierz-Alejska, H Seyfriedowa, A Nowak, J Bodzak
    日期:
    1996-01-01

    A very rare Rhnull phenotype as a cause of haemolytic anaemia in a female patients was for the first time detected in Poland. The beneficial influence of splenectomy was demonstrated. It was proved that a single transfusion of Rh negative red cell concentrate, because of the lack of Rhnull blood, did not cause any acute adverse reactions. However, a transient, subclinical delayed haemolytic reaction due to the stimulation of anti-c and anti-e was observed.

  3. JCR分区: Q4 CAS分区: N/A 影响因子: 0.6

    3. [Unclassified chronic myeloproliferative Ph(-); i(17q); +8 syndrome with mixed myelo-megakaryoblastic crisis--case report].

    PMID:
    作者:
    B Mariańska, D Apel, I Seferyńska, S Maj
    日期:
    1996-01-01

    We present a case of a 17-year old patient with extreme hepatosplenomegaly, hyperthrombocytosis, hyperleucocytosis and the presence of myelo- and megakaryoblasts in the peripheral blood film. Numerous complications that occurred in the course of the disease made cytostatic treatment difficult. Since Ph chromosome and hybrid gene bcr/abl were absent, the diagnosis of unclassified chronic myeloproliferative syndrome in the phase of blast crisis was established. Immunophenotyping confirmed a mixed myelo- megakaryoblastic character of the crisis. In the differential diagnosis other myeloproliferative syndromes were taken into account including i(17q) syndrome. The patient died after a 13-month observation due to neoplasm progression and sepsis.

  4. JCR分区: Q4 CAS分区: N/A 影响因子: 0.6

    4. Acute myelofibrosis in children: report on two cases.

    PMID:
    作者:
    J S Maj, K Rosłan, B Fic-Sikorska
    日期:
    1996-01-01

    In our report, myelofibrosis in children is discussed and two cases of acutely developing myelofibrosis in association with acute megakaryoblastic leukaemia (M7) are presented. In the first case (girl, 34 months), it was acute myelofibrosis of hypocellular marrow. Diagnosis of M7 was confirmed by positive reaction of blasts from peripheral blood with CD42 and CD61 monoclonal antibodies. In the other child (girl, 5 years old), Ph1(+) chronic myeloid leukaemia diagnosed 22 months earlier transformed to M7. Similar to the first case, no marrow aspirate could be obtained and the diagnosis of M7 was made by the bone marrow histology that showed the presence of grossly fibrosed, hypercellular marrow with a large number of dysplastic, maturing megakaryocytes. Neither of the children had Down's syndrome. Although according to FAB classification both cases represent the same haematological entity, their clinical and histopathological presentations are very different.

  5. JCR分区: Q4 CAS分区: N/A 影响因子: 0.6

    5. [Transthyretin and albumin in cerebrospinal fluid in patients with acute leukemias or lymphomas of high grade malignancy].

    PMID:
    作者:
    B Millo, B Zdziarska, P Nowacki
    日期:
    1996-01-01

    Transthyretin and albumin in lumbar cerebrospinal fluid (CSF) and in serum were repeatedly assessed in 40 patients with acute leukemias or high grade non-Hodgkin's lymphomas. The patients were divided into 3 groups. Group I-5 individuals with clinical manifestations of leukemic or lymphomatous meningosis; Group II-33 cases with no clinical data of central nervous system involvement by neoplasm (leukemia/lymphoma); Group III-2 patients in whom extramedullary solid leukemic or lymphomatous infiltrations were diagnosed. It was revealed that blood-brain-barrier dysfunction due to neoplastic infiltration of leptomeninges went with an increase of albumin blood-CSF barrier dependent- and with decrease of blood-CSF barrier-independent transthyretin concentrations. In patients with extramedullary tumors an evident increase of albumin and total-CSF transthyretin and no blood-CSF barrier-independent transthyretin concentrations below the tumor location were observed. It can betray a complete block of the vertebral canal subarachnoid space below the neoplastic compression of the spinal cord. Cytostatics application, either general or intrathecal, did not influence the CSF albumin and transthyretin levels.

  6. JCR分区: Q4 CAS分区: N/A 影响因子: 0.6

    6. [The frequency of cytomegalovirus infection (CMV) in patients immunocompromised patients with malignant and nonmalignant blood disorders].

    PMID:
    作者:
    B Zawilińska, D Weglarska, A M Gruszka, A B Skotnicki, I Zgórniak-Nowosielska
    日期:
    1996-01-01

    Studies on CMV infection were carried out in a group of 110 patients, aged from 15 to 78 (average 38), treated in the Department of Haematology. During the course of observation most of the patients were examined repeatedly. Diagnosis was based on serology (CFT, ELISA) and virus isolation from the clinical material. Primary infection (seroconversion) was confirmed in 4 (21%) out of 19 seronegative patients. Seropositive patients comprised 83 per cent. Active CMV infection was determined in 20 (22%) of those patients.

  7. JCR分区: Q4 CAS分区: N/A 影响因子: 0.6

    7. [Techniques of positive isolation of CD34(+) cells. Personal experience with the immunomagnetic method].

    PMID:
    作者:
    M Markiewicz, H Kamińska, J Wojnar, K Jagoda, M Krawczyk, J Hołowiecki
    日期:
    1996-01-01

    In this article the contemporary methods of positive stem cells isolation have been reviewed, with special regard to their application in the hematological transplantology, and the results of our own studies on isolation with the immunomagnetic method have been presented.

  8. JCR分区: Q4 CAS分区: N/A 影响因子: 0.6

    8. [Treatment of multiple myeloma--present status and perspectives].

    PMID:
    作者:
    T Robak
    日期:
    1996-01-01

    Multiple myeloma (MM) remains incurable. Despite many chemotherapy programs for large numbers of patients, there has been little improvement in outcome during the past 25 years. For many years, intermittent courses of melphalan and prednisone have represented the standard chemotherapy for newly diagnosed symptomatic MM. Many other drug combinations have been assessed, including regimens using multiple alkylating agents, and programs with vincristine, or an anthracycline, and have failed to show any superiority to melphalan-prednisone. Interferon alpha (IFN alpha) inhibits plasma cell growth and has induced responses in approximately 15% of previously untreated patients. This cytokine may have a role when used in those patients who have reached a good "plateau phase" with low tumor burden at the end of a chemotherapeutic program or after a transplantation procedure. The results of myeloablative therapy with allogenic or autologous marrow transplantation are promising and suggest possibility of a cure in some patients. Important problem in the management of MM patients is the treatment of complications, especially bone destruction, hypercalcemia, anemia and infections. Experimental modalities, especially immunotherapy, hold promise for use in humans and may also provide further insights into the pathogenesis of MM.

  9. JCR分区: Q4 CAS分区: N/A 影响因子: 0.6

    9. [Bone marrow changes in patients with hairy cell leukemia after 2-chlorodeoxyadenosine treatment].

    PMID:
    作者:
    I Urasiński, B Zdziarska, A Krygier-Stojałowska
    日期:
    1996-01-01

    Bone marrow abnormalities were assessed in 6 patients with hairy cell leukemia after 2-chlorodeoxyadenosine treatment. In spite of clinical and haematological remission in all patients, hairy cells and fibrosis were found within the marrow. However, the hairy cells number, the thickness of argentophilic fibres and the extent of fibrosis. It was stressed that in addition to histological analysis with hematoxylin-eosin also other stainings for fibrosis should be applied in the bone marrow evaluation, followed by immunohistochemical and molecular methods which allow to exclude minimal residual disease after leukemia treatment.

  10. JCR分区: Q4 CAS分区: N/A 影响因子: 0.6

    10. Leukemic cells growth fraction in the central nervous system in blastic phase of chronic myelogenous leukemia.

    PMID:
    作者:
    B Zdziarska, P Nowacki
    日期:
    1996-01-01

    Clinical and neuropathological investigations were carried out in 6 patients, deceased due to blastic phase of chronic myelogenous leukemia (BPCML). Growth fraction of leukemic cells in peripheral blood, cerebrospinal fluid and in the central nervous system (CNS) was studied, using mitotic index and immunohistochemical staining technique with the monoclonal antibody antiproliferating cell nuclear antigen (anti-PCNA). The results suggest that in BPCML the proliferative activity of leukemic cells is low both in peripheral blood, cerebrospinal fluid, cerebral leukostasis and within the leptomeningeal and intracerebral infiltrates, even in cases with a very high white blood cells count. It can confirm the opinion that in BPCML, accumulation rather than proliferation of leukemic cells plays an important role in the development of the CNS leukemia.

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