A 26-year-old woman, diagnosed with diffuse large B-cell lymphoma, was treated with CHOP (cyclophosphamide, hydroxydaunomycin, oncovin, prednisone), rituximab and radiotherapy. She developed transfusion-dependant anaemia, which persisted following chemotherapy. Bone marrow aspirate and biopsy were consistent with pure red cell aplasia and parvovirus infection. Serology was negative for previous or acute infection but parvovirus DNA was detected by polymerase chain reaction. Administration of intravenous immunoglobulin (1 g/kg) resulted in reticulocytosis and recovery of her haemoglobin. We hypothesize that rituximab caused depletion of her normal B cells, resulting in an inability to mount a primary immune response to parvovirus infection
Abstract Recent reports document resolution of human parvovirus B19-related pure red blood cell apl...
The association between pure red cell aplasia (PRCA) and autoimmune haemolytic anaemia (AIHA) has ra...
Pure red cell aplasia is a bone marrow failure characterized by a progressive normocytic anemia and ...
PubMedID: 30777553Parvovirus B19 is a single-stranded DNA virus that typically has an affinity for e...
Parvo B19 is a single stranded DNA virus, which typically has affi nity for erythroid progenitor cel...
Parvovirus B19 is recognized as a rare cause of pure red cell aplasia (PRCA) in allogeneic stem cell...
A case of pure red cell aplasia in a simultane-ous kidney-pancreas transplant recipient on immunosup...
Copyright © 2011 Panagiotis Tsirigotis et al. This is an open access article distributed under the C...
Differential diagnosis for anemia late after allogeneic stem cell transplantation is broad. In this ...
Human Parvovirus infection is associated with transient aplastic crisis as a most common complicatio...
Sangre (Barc). 1998 Feb;43(1):67-9. Pure red cell aplasia due to persistent B19 parvovirus infectio...
A 61-year-old woman with metastatic renal cell carcinoma underwent systemic treatment with high-dose...
A case of parvovirus B19-induced pure red cell aplasia occurring in a heart transplant recipient is ...
In our Paediatric Clinic we observed a case of transient aplastic crisis caused by Parvovirus B19 in...
Reactivation of human parvovirus B19 is exceptional and characteristic of immunosuppressio...
Abstract Recent reports document resolution of human parvovirus B19-related pure red blood cell apl...
The association between pure red cell aplasia (PRCA) and autoimmune haemolytic anaemia (AIHA) has ra...
Pure red cell aplasia is a bone marrow failure characterized by a progressive normocytic anemia and ...
PubMedID: 30777553Parvovirus B19 is a single-stranded DNA virus that typically has an affinity for e...
Parvo B19 is a single stranded DNA virus, which typically has affi nity for erythroid progenitor cel...
Parvovirus B19 is recognized as a rare cause of pure red cell aplasia (PRCA) in allogeneic stem cell...
A case of pure red cell aplasia in a simultane-ous kidney-pancreas transplant recipient on immunosup...
Copyright © 2011 Panagiotis Tsirigotis et al. This is an open access article distributed under the C...
Differential diagnosis for anemia late after allogeneic stem cell transplantation is broad. In this ...
Human Parvovirus infection is associated with transient aplastic crisis as a most common complicatio...
Sangre (Barc). 1998 Feb;43(1):67-9. Pure red cell aplasia due to persistent B19 parvovirus infectio...
A 61-year-old woman with metastatic renal cell carcinoma underwent systemic treatment with high-dose...
A case of parvovirus B19-induced pure red cell aplasia occurring in a heart transplant recipient is ...
In our Paediatric Clinic we observed a case of transient aplastic crisis caused by Parvovirus B19 in...
Reactivation of human parvovirus B19 is exceptional and characteristic of immunosuppressio...
Abstract Recent reports document resolution of human parvovirus B19-related pure red blood cell apl...
The association between pure red cell aplasia (PRCA) and autoimmune haemolytic anaemia (AIHA) has ra...
Pure red cell aplasia is a bone marrow failure characterized by a progressive normocytic anemia and ...