نتایج جستجو برای: chronic myeloproliferative disorder

تعداد نتایج: 1043759  

2015
Joslin M. Bowen Anamarija M. Perry Erin Quist Mojtaba Akhtari

Chronic myelomonocytic leukemia (CMML) is a clonal hematopoietic malignancy with features of both a myeloproliferative neoplasm and a myelodysplastic syndrome. Even though extramedullary leukemic infiltration is common in CMML patients, lymph node involvement has rarely been reported in the literature. We present an unusual case of a 72-year-old female who was found to have extramedullary hemat...

Journal: : 2022

Chronic myeloid leukemia is a ph-positive myeloproliferative disease, which usually manifested by hyperleukocytosis and massive splenomegaly. rare in childhood adolescence, it accounts for 2 to 3 % of all leukemias cases. priapism manifestation chronic an urgent urological condition that requires timely treatment prevent long-term complications, particular, erectile dysfunction.This review pres...

2017
Romeo-Gabriel Mihăilă

A complete blood count performed in chronic hepatitis C virus (HCV) infected patients can identify thrombocytopenia or an increased number of platelets, the cause of which must be established. Most of these patients are predisposed to develop thrombocytopenia as the disease progresses due to a lower thrombopoietin production, increased platelet pooling in the spleen, viral bone marrow suppressi...

2014
Pontus Lundberg Hitoshi Takizawa Lucia Kubovcakova Guoji Guo Hui Hao-Shen Stephan Dirnhofer Stuart H. Orkin Markus G. Manz Radek C. Skoda

The majority of patients with myeloproliferative neoplasms (MPNs) carry a somatic JAK2-V617F mutation. Because additional mutations can precede JAK2-V617F, it is questioned whether JAK2-V617F alone can initiate MPN. Several mouse models have demonstrated that JAK2-V617F can cause MPN; however, in all these models disease was polyclonal. Conversely, cancer initiates at the single cell level, but...

2015
A Ghotaslou F Nadali B Chahardouli N Alizad Ghandforosh SH Rostami K Alimoghaddam A Ghavamzadeh

BACKGROUND Myeloproliferative disorders are a group of diseases characterized by increased proliferation of myeloid lineage. In addition to JAK2V617F mutation, several mutations in the c-MPL gene have been reported in patients with philadelphia-negative chronic myeloproliferative disorders that could be important in the pathogenesis of diseases. The aim of the present study was to investigate t...

Journal: :Journal of clinical pathology 2003
J Böhm S Kock H E Schaefer P Fisch

BACKGROUND Chronic neutrophilic leukaemia (CNL) is a rare myeloproliferative disorder of elderly patients characterised by sustained neutrophilia and splenomegaly. The diagnosis of CNL requires the exclusion of BCR/ABL positive chronic myelogenous leukaemia (CML) and of leukaemoid reactions (LRs). The differentiation between CNL and LR is problematic because both conditions share similar morpho...

Journal: :Haematologica 1994
T Tison F Vianello P Radossi A Girolami D Sgarabotto F Dazzi

We describe a case characterized by the onset of bone marrow hypoplasia. After treatment with steroid and anabolic compounds, it evolved into a myelodysplastic syndrome (MDS) as demonstrated by morphological and karyotypic analysis. Despite the dysplastic nature of the disorder, a unique feature was its association with a high platelet count. The pathogenesis of the thrombocytosis could not be ...

2010
Young-Hyo Lim Young Yiul Lee Jae Hoon Kim Jinho Shin Jae Ung Lee Kyung-Soo Kim Soon-Kil Kim Jeong Hyun Kim Heon Kil Lim

Essential thrombocythemia (ET) is a chronic myeloproliferative disorder with a prolonged clinical course. Since this disorder is considered to be at increased risk of thromboembolism, therapy is mainly focused on the decreased risk of thrombohemorrhagic events by use of cytotoxic agents. Anagrelide is a phosphodiesterase III inhibitor which is utilized in the treatment of ET for the reduction o...

Journal: :Blood 2000
A A Axelrad D Eskinazi P N Correa D Amato

Hematopoietic progenitor cells in 2 myeloproliferative disorders, juvenile chronic myelomonocytic leukemia and polycythemia vera, are known to be hypersensitive to cytokines that control normal progenitor cell proliferation, differentiation, and survival in their respective granulocyte/macrophage and erythroid lineages. Because thrombopoietin controls these functions in the normal megakaryocyti...

Journal: :Haematologica 1994
M L Randi C Rossi E Barbone G Cavatton F Fabris A Girolami

BACKGROUND The clonal origin of myeloproliferative disorders has been clearly demonstrated and it is known that reactive thrombocytosis occurs as a non specific response to various inflammatory or neoplastic conditions. Only a few papers have discussed the topic of myeloproliferative diseases in blood donors. MATERIALS AND METHODS We report 8 cases of myeloproliferative diseases (3 polycythem...

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