A 2-month-old boy with hemolytic anemia and reticulocytopenia following intravenous immunoglobulin therapy for Kawasaki disease: a case report and literature review [PDF]
Korean Journal of Pediatrics, 2016 Herein, we report a rare case of hemolytic anemia with reticulocytopenia following intravenous immunoglobulin therapy in a young infant treated for Kawasaki disease.
Na Yeon Kim, Soo Hyun Kim, Dong Hyun Cha
exaly +4 more sources
Hard-To-Treat Idiopathic Refractory Autoimmune Haemolytic Anaemia with Reticulocytopenia
European Journal of Case Reports in Internal Medicine, 2020 Autoimmune haemolytic anaemia (AIHA) is an uncommon condition characterized by increased destruction of erythrocytes associated with reticulocytosis in the great majority of cases.
Marcelo Aveiro +4 more
doaj +4 more sources
Hyperuricemia and Reticulocytopenia in Association With Autoimmune Hemolytic Anemia in Two Children [PDF]
American Journal of Clinical Pathology, 2004 Hyperuricemia developed in 2 children with autoimmune hemolytic anemia with reticulocytopenia at a time of hemolytic crisis. One likely cause of hyperuricemia is the destruction of nucleated RBC precursors by autoantibodies. It is advised that patients with autoimmune hemolytic anemia with reticulocytopenia be examined for hyperuricemia.
Wu John K, Wadsworth Louis D
exaly +3 more sources
Excessive apoptosis of bone marrow erythroblasts in a patient with autoimmune haemolytic anaemia with reticulocytopenia [PDF]
British Journal of Haematology, 2000 We report a patient with autoimmune haemolytic anaemia (AIHA) with reticulocytopenia, who showed excessive apoptosis of erythroblasts. Ultrastructural analysis of bone marrow cells showed that 50% of erythroblasts had characteristic features of apoptosis, which was confirmed by staining with Annexin‐V.
A A Van De Loosdrecht +2 more
exaly +5 more sources
Vitamin B12 Deficiency‐Associated Pseudo‐Thrombotic Microangiopathy in a Patient on Longstanding Oral B12 Supplementation [PDF]
Clinical Case ReportsVitamin B12 deficiency is a common cause of normocytic or megaloblastic anemia. In 2.5% of cases, it can manifest as pseudo‐thrombotic microangiopathy (pseudo‐TMA), which mimics thrombotic thrombocytopenic purpura (TTP), an emergent hemolytic ...
Hanna K. Bertucci +2 more
doaj +2 more sources
De Novo Variant in the RPL27 Gene in a Second Infant with Diamond-Blackfan Anemia [PDF]
Case Reports in HematologyWe describe a 10-month-old female with Diamond-Blackfan anemia (DBA) who presented with macrocytic anemia and reticulocytopenia. Whole exome sequencing revealed a de novo intronic variant in RPL27 (NM_000988.3:c.-2-1G > A p.?) previously reported in one ...
Joshua Glass +3 more
doaj +2 more sources
THE EVENTS IN THE HEMOLYTIC CRISIS OF HEREDITARY SPHEROCYTOSIS, WITH PARTICULAR REFERENCE TO THE RETICULOCYTOPENIA, PANCYTOPENIA AND AN ABNORMAL SPLENIC MECHANISM [PDF]
Blood, 1948 Abstract The course of hereditary spherocytosis (congenital or familial hemolytic anemia) is subject to major or minor exacerbations or crises. Pancytopenia, reticulocytopenia, and extreme spherocytosis characterize the major crises, during which hypersplenic effects appear to play a major role. These are characterized by the combination
William Dameshek, Dameshek William
exaly +3 more sources
Use of IV immunoglobulin to treat steroid resistant, immune checkpoint inhibitor‐induced pure red cell aplasia: A case report [PDF]
eJHaemPure red cell aplasia (PRCA) is characterised by normocytic normochromic anaemia, reticulocytopenia and reduced erythroid precursors in bone marrow. PRCA as an immune‐related adverse event secondary to immune checkpoint inhibitor (ICI) therapy is rare ...
Sam Sherratt‐Mayhew +1 more
doaj +2 more sources
Congenital Anemia Due to Erythropoietin Gene Mutation Presenting With Diamond–Blackfan Anemia-like features [PDF]
Journal of Investigative Medicine High Impact Case ReportsDiamond–Blackfan anemia (DBA) is an inherited hypoplastic anemia, caused by mutations in ribosomal protein genes. Other mutations such as mutations in the erythropoietin (EPO) gene can lead to DBA-like (DBAL) through impairment of erythropoiesis.
Ibrahim AboGhayyada MD +5 more
doaj +2 more sources