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Toplam kayıt 24, listelenen: 1-20
The Rate of Hepatitis B and C Virus Infections and the Importance of HBV Vaccination in Children with Acute lymphoblastic Leukemia
(2007)
Aim: The aim of the study was to evaluate the rate of hepatitis B and C virus infection and emphasize the importance of hepatitis B virus (HBV) vaccination in leukemic children.
Methods: One hundred and sixty children ...
Hepatitis B Immunoglobulin in Combination with Lamivudine for Prevention of Hepatitis B Virus Reactivation in Children Undergoing Bone Marrow Transplantation
(WILEY, 2006)
Abstract: There is little information in literature about the use of hepatitis B immunoglobulin (HBIg) in recipients of bone marrow transplantation (BMT). Here, we report two children who received IV HBIg (Hepatect‐CP) and ...
Varicella Zoster-Associated Severe Aplastic Anemia in a Child and Its Successful Treatment with Peripheral Blood Stem Cell Transplantation from HLA-5/6-Identical Donor
(ISI, 2007)
Background: Varicella zoster virus is very rarely associated with aplastic anemia. Bone marrow transplantation from an HLA-identical sibling is the treatment of choice.
Case report: A seven-year-old boy presented with ...
Hemophagocytic Syndrome and Acute Liver Failure Associated with Ethylene Glycol Ingestion: A Case Report
(Taylor & Francis, 2006)
The authors describe a case of accidental ethylene glycol poisoning in an 18-month-old boy who developed hemophagocytic syndrome (HPS). Ethylene glycol is a common substance in various antifreeze preparations. Acute ethylene ...
Atypical Skin Graft-vs.-Host Disease Following Bone Marrow Transplantation in an Infant
(Wiley, 2007)
Herein, we describe an unusual presentation of acute graft versus host disease (GVHD) mimicking contact dermatitis in an infant who underwent 5/6 HLA-matched bone marrow transplantation (BMT) from his mother for malignant ...
The 8p11 Myeloproliferative Syndrome in A 3-year-Old Child
(Elsevier, 2007)
We read the interesting report by Wong et al. describing 8p11 stem cell syndrome in a 14-year-old Chinese boy [1]. We wish to report our recent observations on a 3-year-old boy with T-cell lymphoma who was referred to the ...
An Unusual Case of Reactive Lymphocytosis Mimicking Acute Leukemia
(Taylor and Francis, 2007)
The diagnosis of acute leukemia is based on a combination of clinical, hematological, morphological, cytogenetic, and immunophenotypic data. The authors report a case of reactive lymphocytosis with extremely elevated ...
A Prompt Graft-Versus-Thalassemia Effect upon Withdrawal of CyclosporineA in A Child Who Received Allogeneic Peripheral Blood Stem Cell Transplantation
(Nature, 2006)
Stable mixed chimerism is a common event in children with thalassemia major who have undergone bone marrow transplantation (BMT). However, persistence of unstable mixed chimerism in these children is associated with a ...
Transfusion-Transmitted Virus Prevalence in Turkish Patients with Thalassemia
(Taylor & Francis, 2006)
In hematology patients on chronic transfusion regimes, liver diseases are frequent, and mostly related to the agents transmitted by blood products and concominant iron deposition in liver. Besides hepatitis B (HBV) and C ...
Micrococcus Sedentarius Bacteraemia Presenting with Haemophagocytic Syndrome in Previously Healthy Boy
(Taylor and Francis, 2006)
Haemophagocytic syndromes are the clinical manifestation of an increased macrophagic activity with haemophagocytosis. Infection-associated HS was originally described by Risdall in 1979, in viral disease. Since the initial ...
Diamond–Blackfan Anemia Associated Withb-Thalassemia Trait
(WILEY, 2006)
A 14-month-old boy was referred to our hospital for evaluation of severe anemia. In the bone marrow aspiration smear, normal cellularity with severe erythroblastopenia (3%) was observed. The hemoglobin electrophoresis of ...
Dysplasia and Disorder of cell Membrane Entirety in Iron-Deficiency Anemia
(Taylor and Francis, 2008)
Peripheral blood smears of 43 patients (26 males, median age 18 months, range: 6-180 months) with nutritional iron-deficiency anemia (IDA) were examined for the presence of trilineage hematological dysplasia. Twelve patients ...
Hyperacute Graft-vs.-Host Disease After Related HLA-Identical Umbilical Cord Blood Transplantation
(Wiley, 2007)
haGVHD has been described following bone marrow and peripheral blood stem cell transplantation and in a single case who received unrelated HLA mismatched CB. An unusual case of haGVHD following HLA 6/6-matched sibling CBT ...
Intravenous Immunoglobulin in The Treatment of Severe MethotrexateInduced Acral Erythema
(Wolters Kluwer, 2008)
Two New Cases with Pearson Syndrome and Review of Hacettepe Experience
(2008)
SUMMARY: Topaloğlu R, Lebre AS, Demirkaya E, Kuşkonmaz B, Coşkun T,
Orhan D, Gürgey A, Gümrük F. Two new cases with Pearson syndrome and
review of Hacettepe experience. Turk J Pediatr 2008; 50: 572-576.
Pearson syndrome ...
Lymphocytic Vacuolization in Lymphocytic Vacuolization in Sialic Acid Storage Disease Acid Storage Disease
(Wiley, 2008)
Lymphocytic vacuolization in sialic acid storage disease