Results 31 to 40 of about 1,235 (149)

Tacrolimus-Induced Pure Red Cell Aplasia Following Renal Transplantation: A Case Report and Literature Review

open access: yesTurkish 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

A Unique Constitutional Robertsonian Translocation t(13;14) Associated with Severe Aplastic Anaemia [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2021
Aplastic anaemia is characterised by cytopenias and hypocellular bone marrow without any evidence of marrow fibrosis or marrow infiltration. There is no specific cytogenetic abnormality associated with aplastic anaemia.
Bhupendra Singh   +4 more
doaj   +1 more source

Erythropoietin May Improve Anemia in Patients with Autoimmune Hemolytic Anemia Associated with Reticulocytopenia [PDF]

open access: yesTransfusion Medicine and Hemotherapy, 2012
BACKGROUND: Management of patients with autoimmune hemolytic anemia (AIHA) and reticulocytopenia remains challenging. CASE REPORTS: Two patients with decompensated AIHA who were receiving immunosuppressive drugs were treated with erythropoietin (EPO). Administration of EPO increased reticulocyte counts and hemoglobin concentrations in both cases.
Olga, Arbach   +3 more
openaire   +2 more sources

A Rare Case of Parvovirus Infection Causing Pure Red Cell Aplasia in a Kidney-Pancreas Transplant Recipient. [PDF]

open access: yesNephrology (Carlton)
ABSTRACT Parvovirus B19 infection can rarely manifest with pure red cell aplasia in immunocompromised hosts. This case details a 48‐year‐old male, 11 years post kidney‐pancreas transplant who was admitted with a chronic normocytic anaemia (haemoglobin 72 g/L) after being admitted four months prior with a bleeding peptic ulcer, requiring eight units of ...
Perry O   +5 more
europepmc   +2 more sources

Acquired pure red cell aplasia: unraveling the immune pathogenesis

open access: yesJournal 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

Case Report: Pure Red Cell Aplasia due to Angioimmunoblastic T-Cell Lymphoma

open access: yesCase Reports in Oncology, 2020
Pure red cell aplasia (PRCA) is a rare bone marrow failure characterized by a progressive normocytic anemia and reticulocytopenia without leukopenia and thrombocytopenia.
Marina Vitorino   +5 more
doaj   +1 more source

A meta‐analysis of toxicities related to hydroxycarbamide dosing strategies

open access: yeseJHaem, 2020
Due to fear of short‐term toxicities, there is nonconsensus of hydroxycarbamide dosing strategy (escalated vs fixed‐dosing methods), which contributes to its suboptimal use.
Joacy G. Mathias   +9 more
doaj   +1 more source

An Unusual Case of Hyperhemolysis Syndrome and Delayed Hemolytic Transfusion Reaction due to Anti-Jk(a) and Anti-P1 Antibodies

open access: yesCase Reports in Medicine, 2023
Background. Hyperhemolysis syndrome (HS) is a severe hemolytic transfusion reaction that can cause hemoglobin and hematocrit levels to drop below pretransfusion levels, leading to severe anemia.
Hunter Montgomery   +3 more
doaj   +1 more source

Delayed hemolytic transfusion reaction in children with sickle cell disease

open access: yesHaematologica, 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
doaj   +1 more source

Aggressive Systemic Mastocytosis in Association with Pure Red Cell Aplasia

open access: yesCase Reports in Hematology, 2018
Aggressive systemic mastocytosis (ASM) is characterized by mast cell accumulation in systemic organs. Though ASM may be associated with other hematological disorders, the association with pure red cell aplasia (PRCA) is rare and has not been reported ...
Dhauna Karam   +3 more
doaj   +1 more source

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