نتایج جستجو برای: Hemolysis Anemia

تعداد نتایج: 65884  

Journal: :iranian journal of pediatric hematology and oncology 0
narges beigom mirbehbahani associate professor, pediatric hematology and oncology, neonatal and childrens health research center , golestan univeسازمان های دیگر: pediatric hematology and oncology, neonatal and childrens health research center aysan salamikhanshan pediatric hematology and oncology, taleghani hospital, gorgan, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی گلستان (golestan university of medical sciences) baranak safaian assistant professor, pediatric nephrology, department of pediatric nephrology, golestan university of medical sciences,سازمان اصلی تایید شده: دانشگاه علوم پزشکی گلستان (golestan university of medical sciences) sakineh mohammadian associate professor, pediatrician, department of pediatric, golestan university of medical sciences, gorgan, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی گلستان (golestan university of medical sciences) nasser behnampour assistant professor, biology statistic, department of hygiene , golestan university of medical sciences, gorgan, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی گلستان (golestan university of medical sciences) safa ariannejad pediatrician, department of pediatric, taleghani hospital, gorgan, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی گلستان (golestan university of medical sciences)

background: sodium bicarbonate serum therapy is used for compensation bicarbonate lost and increasing blood ph in metabolic acidosis caused by severe anemia in patient with glucose-6-phosphate dehydrogenase (g6pd) deficiency. the aim of present study was comparison the effect of serum therapy using two different serums (serum with bicarbonate and without bicarbonate) on some renal and hematolog...

Journal: :American practitioner and digest of treatment 1949
C WILLIAMS A F GODLEY

Hemolysis presents as acute or chronic anemia, reticulocytosis, or jaundice. The diagnosis is established by reticulocytosis, increased unconjugated bilirubin and lactate dehydrogenase, decreased haptoglobin, and peripheral blood smear findings. Premature destruction of erythrocytes occurs intravascularly or extravascularly. The etiologies of hemolysis often are categorized as acquired or hered...

Journal: :iranian journal of pediatric hematology and oncology 0
leila tahmasebi hematology research center, shiraz university of medical sciences, shiraz, iran sezaneh haghpanah hematology research center, shiraz university of medical sciences, shiraz, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی شیراز (shiraz university of medical sciences) narges rezaei hematology research center, shiraz university of medical sciences, shiraz, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی شیراز (shiraz university of medical sciences) mehran karimi hematology research center, shiraz university of medical sciences, shiraz, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی شیراز (shiraz university of medical sciences)

abstract background: hereditary red cell enzyme disorders are a group of non-immune/spherocytic hemolytic anemia, although these disorders are rare and they have not public health problems, the detection of these defects could help to physician in treatment and differential diagnosis. this study evaluated 5 enzymopathies in patients with hereditary non –immune/spherocytic hemolytic anemia (hnsh...

2009
Sharon A. Center

Differential Diagnosis of Hemolytic Anemia Hemolytic anemia reflects shortened RBC life span due to intravascular, extravascular, or fragmentation hemolysis. Intravascular hemolysis is primarily associated with type 1 hypersensitivity reactions, either idiopathic or secondary to another primary disease. In some cases an infectious intraerythrocytic or epierythrocytic agent or miscellaneous diso...

2017
Saki Todo Kohei Okamoto Takeshi Sugimoto Toshimasa Takahashi Yasushi Nakagawa Takashi Arai Katsuhito Nishiyama Kenta Hara Yoshiro Yasutomo Koichi Yokono

An 80-year-old female was admitted to our hospital due to malaise. The initial diagnosis on admission was pernicious anemia (PA), Hashimoto thyroiditis and autoimmune atrophic gastritis. Autoimmune hemolytic anemia was suspected because direct antiglobulin test (DAT) was positive. Treatment with vitamin B12 improved anemia, with the disappearance of hemolysis. In some cases, PA patients with po...

2007
Ümit Çelik Göksel Leblebisatan Emre Alhan Necmi Aksaray

11 Summary Despite the fact that anemia is one of the most striking clinical features of visceral leishmaniasis (kala-azar), the factors involved in the pathogenesis are not fully understood. The cause of anemia seen in these patients is often multifactorial including sequestration and destruction of the erythrocytes in the enlarged spleen, hemophagocytosis and alterations in erythrocyte membra...

Journal: :Journal of the College of Physicians and Surgeons--Pakistan : JCPSP 2008
Syed Qamar Abbas Nasiruddin Mohammed Misfer Al-Gethami

A 60-year-old male patient presented with jaundice. Initial investigations showed anemia, indirect hyperbilirubinemia, raised Lactic Dehydrogenase (LDH) and increased reticulocyte count suggestive of hemolysis. Considering hemolysis low MCV and basophilic stippling on peripheral film, hemoglobin electrophoresis was done that showed Haemoglobin H (15.5%) that in the absence of family history was...

2015
Scott M Lee Duvuru Geetha

Dapsone is a commonly used second line drug for prophylaxis of pneumocystis jirovecii pneumonia (PJP) in immunocompromised patients. Oxidant hemolysis, caused by dapsone's metabolite hydroxylamine, is a common side effect, and screening for glucose-6-phosphate dehydrogenase (G6PD) deficiency is recommended before the drug is started in order to prevent potential hemolytic reactions. We report a...

Journal: :American journal of hematology 2003
M Deutsch S P Dourakis K Papanikolopoulos M Belegrati T Kalmantis

Autoimmune hemolytic anemia (AIHA) has been described in patients with lymphoid neoplasm with an etiologic relationship between the emergence of autoantibodies and lymphocyte dysfunction. Autoimmune disorders are less to develop in patients with other neoplasm like chronic myeloid leukemia, myelodysplastic syndrome or acute myeloid leukemia. Few reports have been documented the development of i...

2015
Andrea O Akpoguma Thomas L Carlisle Steven R Lentz

BACKGROUND Paroxysmal cold hemoglobinuria is caused by a biphasic IgG autoantibody that triggers complement-mediated intravascular hemolysis. Paroxysmal cold hemoglobinuria has not previously been reported to occur in association with pregnancy. CASE PRESENTATION We report a case of an 18 year old female who presented in early pregnancy with acute hemolytic anemia and a positive Donath-Landst...

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