نتایج جستجو برای: thrombocytosis

تعداد نتایج: 2274  

Journal: :Haematologica 2000
V Chanet O Tournilhac V Dieu-Bellamy N Boiret P Spitz O Baud C Darcha P Travade H Laurichesse

Thrombocytosis is a common feature of myeloproliferative disorders but may also result from various conditions including chronic iron deficiency, hemorrhage, chronic inflammation and splenectomy. We report two cases of secondary thrombocytosis caused by isolated and congenital asplenia, mimicking essential thrombocythemia. These two adult cases of spleen agenesis were unexpected. We conclude th...

Journal: :Journal of clinical pathology 2000
M R Howard S Ashwell L R Bond I Holbrook

AIM To investigate possible abnormalities of serum potassium and calcium levels in patients with essential thrombocythaemia and significant thrombocytosis. METHODS 24 cases of essential thrombocythaemia with significant thrombocytosis (platelet count > 700 x 10(9)/litre) had serum potassium and calcium estimations performed at the time of maximum thrombocytosis before treatment, and at the ti...

Journal: :Indian pediatrics 2008
E Mantadakis A Tsalkidis A Chatzimichael

Thrombocytosis is a frequent finding in hemograms obtained from hospitalized and ambulatory children due to the widespread use of automated blood cell counters. Pediatricians are commonly puzzled in cases of thrombocytosis to determine the underlying cause and the need for therapy. The purpose of this review is to assist the general pediatrician into dealing with this common hematological findi...

Journal: :Journal of microbiology, immunology, and infection = Wei mian yu gan ran za zhi 2006
Chih-Yang Lin Yao-Hsu Yang Chien-Chang Lee Chou-Lang Huang Li-Chieh Wang Bor-Luen Chiang

BACKGROUND AND PURPOSE Depending on the severity of the illness, thrombocytosis is found in about 60% to 70% of patients with Henoch-Schönlein purpura (HSP). Whether thrombocytosis is the result of an inflammatory reaction mediated by thrombopoietin (TPO) or other inflammatory cytokines such as interleukin (IL)-6 remains unknown. METHODS Thirty two patients who met the diagnostic criteria for...

Journal: :Annals of the rheumatic diseases 1978
S M Rajah

Thrombocytosis may occur in association with autoimmune, collagen, and malignant diseases (Levin and Conley, 1964; Bean, 1965; Selroos, 1972; Davis and Mendez Ross, 1973). In rheumatoid arthritis a positive correlation has been found between the platelet count and disease activity (Bean, 1965; Selroos, 1972; Hryszko et al., 1975; Hemandez, 1975; Hutchinson et al., 1976). Thrombosis is infrequen...

Journal: :The Pediatric infectious disease journal 2012
Valerio Cecinati Letizia Brescia Susanna Esposito

In both children and adults, thrombocytosis is usually defined as a platelet count of more than 450 10/ L. As there are many primary and secondary causes, as well as false or “spurious” conditions mimicking thrombocytosis, establishing the cause requires considering clinical features and hematologic parameters. Pediatric primary thrombocytosis is very rare, but reactive thrombocytosis (RT) can ...

Journal: :JPMA. The Journal of the Pakistan Medical Association 2013
Naushad Abid

Systemic lupus is an autoimmune disease of worldwide distribution. The disease is characterized clinically by multisystem manifestations. Haematological manifestations are diverse. Thrombocytosis has rarely been reported in association with SLE and may occur as a result of active disease or reactive due to underlying inflammatory process. Our patient was a 14 years old female who was diagnosed ...

Journal: :international journal of hematology-oncology and stem cell research 0
majid vafaie research center of thalassemia & hemoglobinopathy, ahvaz jundishapur university of medical sciences, ahvaz, iran. kaveh jaseb research center of thalassemia & hemoglobinopathy, ahvaz jundishapur university of medical sciences, ahvaz, iran. majid ghanavat research center of thalassemia & hemoglobinopathy, ahvaz jundishapur university of medical sciences, ahvaz, iran. mohamad pedram research center of thalassemia & hemoglobinopathy, ahvaz jundishapur university of medical sciences, ahvaz, iran. tooran rahiminia research center of thalassemia & hemoglobinopathy, ahvaz jundishapur university of medical sciences, ahvaz, iran.

essential thrombocythemia is a rare myeloproliferative disorder in pediatrics. this myeloproliferative disorder is charactherized by thrombocytosis and hyperplasia of megakaryocytes in the bone marrow. other cell lines are not involved.jak2v617fmutations has been identified in approximately half the patients with this disorder. we describe a 12-year-old boy with essential throbocythemia. the pa...

Journal: :Blood 1977
R R Streeter C A Presant E Reinhard

In order to determine the prognostic significance of thrombocytosis in idiopathic sideroblastic anemia, the clinical courses of 17 patients were reviewed. Six patients (36%) had thrombocytosis, and none developed acute leukemia. Nine patients (53%) had normal platelet counts, and one developed acute leukemia. Two patients (12%) were thrombocytopenic, and one died of acute leukemia. There was li...

Journal: :Baylor University Medical Center Proceedings 2009

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