Delayed hemolytic transfusion reaction in children with sickle cell disease [PDF]
Haematologica, 2011 Background Transfusion is a cornerstone of the management of sickle cell disease but carries a high risk of hemolytic transfusion reaction, probably because of differences in erythrocyte antigens between blood donors of European descent and patients of ...
Mariane de Montalembert +8 more
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RIFAMPICIN INDUCED PURE RED CELL APLASIA [PDF]
Zdravniški Vestnik, 2008 BACKGROUND Pure red cell aplasia (PRCA) is a rare condition of severe anemia characterized by anabsence of erythroid precursor in the bone marrow, severe reticulocytopenia and normalplatelet and leukocyte count.
Marija Čeh
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Preservative Monitoring of a Greek Woman with Hydrops Fetalis due to Parvovirus B19 Infection
Case Reports in Obstetrics and Gynecology, 2017 Primate erythroparvovirus 1 (parvovirus B19) is a member of the Erythrovirus genus of the Parvoviridae family and it is one of the few members of the family known to be pathogenic in human.
Zacharias Fasoulakis +2 more
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Rapid Recovery from Chronic PRCA by MSC Infusion in Patient after Major ABO-Mismatched alloSCT [PDF]
Case Reports in Medicine, 2012 Pure red cell aplasia (PRCA) is a rare complication in recipients of allogenic stem cell from ABO incompatible donors. It is characterized by reticulocytopenia and by an absence of red cell cell precursors in the bone marrow.
Vera Sergeevicheva +8 more
doaj +2 more sources
Pediatric Hematology Oncology JournalVitamin B12 is vital for physiological functions, and its deficiency is relatively frequent in individuals residing in lower-middle-income countries (LMIC).
Mohd Arif, Nazish Malik
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Vitamin B12 Deficiency Mimicking Thrombotic Microangiopathy: A Case of Pseudo-Thrombotic Microangiopathy. [PDF]
J Community Hosp Intern Med PerspectINTRODUCTION: Vitamin B12 deficiency may rarely present with hemolysis and schistocytosis, mimicking thrombotic microangiopathy (TMA). This pseudo-TMA variant is clinically significant, as delayed recognition may lead to unnecessary treatments and ...
Pillai M +4 more
europepmc +4 more sources
Successful Treatment of Pure Red Cell Aplasia in Systemic Lupus Erythematosus With a Combination of Rituximab and Mycophenolate Mofetil. [PDF]
CureusPure red cell aplasia (PRCA) is a rare cause of severe anaemia characterized by selective erythroid suppression in the bone marrow with preservation of other haematopoietic lineages. Its association with systemic lupus erythematosus (SLE) is uncommon and
Carvalho MC +4 more
europepmc +2 more sources
Novel Cases of Diamond Blackfan Anaemia in Two Nigerian Toddlers: Roadmap for Care in Resource-Limited Nations [PDF]
International Journal of Scientific Research in Dental and Medical Sciences, 2021 Diamond Blackfan anaemia (DBA) is a rare cause of anaemia in children. To the best of our knowledge, these are the first cases reported in Nigeria. Two toddlers with a history of recurrent anaemia, which started within the first three months of life ...
Thomas Ulasi +3 more
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THE SEROPOSITIVITY OF PARVOVIRUS B19 AMONG KIDNEY TRANSPLANT RECIPIENTS
The Iraqi Journal of Medical Sciences, 2017 Background: Parvovirus B19 (PV-B19) is a single strand DNA virus that is responsible for causing several diseases in humans. Parvovirus B19 induced persistent anemia or/and pancytopenia or/and reticulocyteopenia in renal transplant recipients (RTRs ...
Zainab A. Hlail +2 more
doaj +6 more sources
Pure red cell aplasia, a disease of a great diversity
Journal of Applied Hematology, 2020 Pure red cell aplasia (PRCA) is a type of normocytic or sometimes macrocytic anemia characterized by reticulocytopenia. The cause of hypo erythropoiesis is varied. It could be of a congenital or an acquired type.
Mona M Alfaraj, Hussain H Al Saeed
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