Now showing items 1-20 of 24
An Unusual Presentation of Pediatric Acute Lymphoblastic Leukemia with Parotid Gland Involvement and Dactylitis
(Aves Yayincilik, 2010)
Mumps infection during the course of childhood acute lymphoblastic leukemia (ALL) treatment has been reported to have a mild course and this was related to the intrinsic low cytopathological effect of the virus, contrasting ...
Fanconi Anemia: A Single Center Experience Of A Large Cohort
Fanconi anemia (FA) is an inherited disease, characterized by congenital malformations, short stature, progressive bone marrow failure and predisposition to leukemia and solid tumors. The aim of this study was to evaluate ...
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 ...
Number of Erythrocyte Transfusions is more Predictive than Serum Ferritin in Estimation of Cardiac Iron Loading in Pediatric Patients with Acute Lymphoblastic Leukemia.
Background Transfusions with packed erythrocytes is a common practice in pediatric patients with acute lymphoblastic leukemia (ALL) who are on chemotherapy. Since there is no physiological excretion mechanism for iron, ...
Infant lymphoblastic Leukemia: A Single Centers 10 Year Experience
Yaman-Bajin İ, Aytaç S, Kuşkonmaz B, Uçkan-Çetinkaya D, Ünal Ş, Gümrük F, Çetin M. Infant lymphoblastic leukemia: a single centers 10 year experience. Turk J Pediatr 2019; 61: 325-329. Infant acute lymphoblastic leukemia ...
Acute Promyelocytic Leukemia in a Child with Reticulin Fibrosis
Fanconi Anemia: A Single Center Experience of a Large Cohort
(Hacettepe Medical Center, 2019)
Diamond–Blackfan Anemia Associated Withb-Thalassemia Trait
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 ...
Two New Cases with Pearson Syndrome and Review of Hacettepe Experience
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 ...
The Clinical and Laboratory Evaluation of Familial Hemophagocytic Lymphohistiocytosis and the Importance of Hepatic and Spinal Cord Involvement: A Single Center Experience
Familial hemophagocytic lymphohistiocytosis is an autosomal recessive, life-threatening condition characterized by defective immune response. A retrospective analysis was performed on 57 patients diagnosed with familial ...
Lymphocytic Vacuolization in Lymphocytic Vacuolization in Sialic Acid Storage Disease Acid Storage Disease
Lymphocytic vacuolization in sialic acid storage disease