Results 31 to 40 of about 1,434 (146)
DNA Methyl Transferase 3A (DNMT3A) Mutation Presenting as Isolated Pure Red Cell Aplasia
Journal of Investigative Medicine High Impact Case Reports, 2022 Pure red cell aplasia (PRCA) is a rare disorder mainly affecting the erythroid precursor cells. It presents with severe isolated reticulocytopenia with relatively normal counts in the myeloid and megakaryocytic lineages.
Adarsh Sidda MD +4 more
doaj +1 more source
Current Medicine Research and Practice, 2022 Aplastic anaemia can develop due to various viral infections. However, SARS-CoV-2 infection evolving into aplastic anaemia is rarely seen. Here, we present a case of a 6-year-old boy who presented with epistaxis and rashes all over the body after ...
Akanksha Bhatia +2 more
doaj +1 more source
Idiopathic pure red cell aplasia: A case series from India
Asian Journal of Medical Sciences, 2023 Pure red cell aplasia (PRCA) is a rare hematologic disorder characterized by normocytic normochromic anemia with reticulocytopenia and depleted erythroid precursors. It is reported mainly from western countries.
Manoj U Mahajan +9 more
doaj +1 more source
Терапевтический архив, 2019 Eight patients were observed with a rare combination of thymoma and pure red cell aplasia of bone marrow (PRCA), of which seven women were between 44 to 68 years old.
A A Petrenko +3 more
doaj +1 more source
, 2021 Background: Hemolytic disease of the fetus and newborn (HDFN) attributable to anti-M is rare, although case reports implicate anti-M in varying severities of HDFN, including fetal hydrops and intrauterine death.
Lezlie H. Andersen +13 more
core +1 more source
Successful treatment of tacrolimusâ related pure red cell aplasia and autoimmune hemolytic anemia with rituximab in a pediatric cardiac transplant patient [PDF]
, 2017 Acquired pure red cell aplasia (PRCA) and autoimmune hemolytic anemia (AIHA) are rare complications of immunosuppression in pediatric solid organ transplant patients.
Abongwa, Chenue +5 more
core +1 more source
Turkish Journal of Nephrology, 2021 Anemia is common in end-stage renal disease, but it resolves rapidly after transplantation due to normalization of kidney function. Acquired pure red cell aplasia (PRCA) is an infrequent complication in kidney recipients. PRCA is a rare cause of profound
Dilek Barutçu Ataş +5 more
doaj +1 more source
Isoniazid-triggered pure red cell aplasia in systemic lupus erythematosus complicated with myasthenia gravis. [PDF]
, 2010 A 47-year-old woman who had been treated for systemic lupus erythematosus (SLE) with myasthenia gravis (MG) was admitted to our hospital with acute onset of severe anemia after administration of isoniazid.
Eguchi, Katsumi +7 more
core +1 more source
Acquired pure red cell aplasia: unraveling the immune pathogenesis
Journal of Bio-X Research, 2023 Acquired pure red cell aplasia (aPRCA) is a rare hematological disorder characterized by normochromic, normocytic anemia, reticulocytopenia, and the absence of erythroblasts. The pathogenesis of aPRCA has remained elusive.
Mengyuan Liu +3 more
doaj +1 more source
Diagnosis and Management of Prenatal Hereditary Pyropoikilocytosis
Prenatal Diagnosis, EarlyView.ABSTRACT Hereditary pyropoikilocytosis (HPP) is a severe hemolytic anemia caused by variants in SPTA1, SPTB, and EPB41. These weaken horizontal interactions in the erythrocyte cytoskeleton, causing membrane fragmentation and splenic sequestration. It will readily cause fetal anemia and often hydrops fetalis. Prenatal diagnosis requires first ruling out
Connor Hartzell +6 more
wiley +1 more source