Results 51 to 60 of about 1,434 (146)
British Journal of Haematology, Volume 208, Issue 5, Page 1797-1805, May 2026.Summary T‐cell abnormalities have been implicated in the pathogenesis of acquired pure red cell aplasia (PRCA), particularly in its major subtypes such as idiopathic PRCA, thymoma‐associated PRCA and large granular lymphocytic leukaemia (LGLL)–associated PRCA, and the precise details remain unclear.
Naruaki Yamashita +11 more
wiley +1 more source
eJHaem, Volume 7, Issue 2, April 2026.ABSTRACT A 28‐year‐old male with paroxysmal nocturnal haemoglobinuria (PNH) presented with headache, nasal bridge discomfort and haemoglobinuria. He developed a macular‐papular rash which rapidly progressed into purpura, necrosis and peri‐orbital oedema. Investigations demonstrated severe haemolytic anaemia and acute parvovirus B19 infection.
Louise J. Potter +9 more
wiley +1 more source
, 2007 The association between pure red cell aplasia (PRCA) and autoimmune haemolytic anaemia (AIHA) has rarely been reported. PRCA represents an isolated process, characterized by normochromic, normocytic anaemia, reticulocytopenia and erythroid hypoplasia in ...
Hassan, Rosline, Ahmed, Suhair Abbas
core +2 more sources
Severe, Refractory Primary Warm Autoimmune Hemolytic Anemia Requiring 90 Erythrocyte Transfusions
Annals of Internal Medicine: Clinical CasesA previously healthy 60-year-old man presented to the hospital with a hemoglobin of 3.5 g/dL. He was diagnosed with severe warm autoimmune hemolytic anemia with reticulocytopenia on hospital day 1 that was not responsive to steroids, immune globulin, and
Neeharika Namineni +3 more
doaj +1 more source
Somatic Mutations in Acquired Pure Red Cell Aplasia: Incidence and Implications
American Journal of Hematology, Volume 101, Issue 7, Page 1554-1555, July 2026.
Robert T. Means Jr
wiley +1 more source
How we evaluate red blood cell compatibility and transfusion support for patients with sickle cell disease undergoing hematopoietic progenitor cell transplantation [PDF]
, 2018 Multiple hematopoietic progenitor cell (HPC) transplantation options for patients with sickle cell disease (SCD) are currently under investigation. Patients with SCD have a high rate of alloimmunization to red blood cell antigens, often complicating ...
Nelson, Randin C +5 more
core +1 more source
Parvovirus B19-triggered acute hemolytic anemia and thrombocytopenia in a child with Evans syndrome
Mediterranean Journal of Hematology and Infectious Diseases, 2018 Background: Human parvovirus B19 (HPV-B19) is the etiologic agent of erythema infectiosum, of transient aplastic crises in individuals with underlying chronic hemolytic disorders, and of chronic pure red cell aplasia in immunocompromised individuals ...
ELPIS MANTADAKIS
doaj +1 more source
Aplastic crisis caused by parvovirus B19 in an adult patient with sickle-cell disease
Revista da Sociedade Brasileira de Medicina Tropical, 2000 We describe a case of aplastic crisis caused by parvovirus B19 in an adult sickle-cell patient presenting with paleness, tiredness, fainting and dyspnea. The absence of reticulocytes lead to the diagnosis.
Sérgio Setúbal +3 more
doaj
Progress towards Mechanism-Based Treatment for Diamond-Blackfan Anemia
The Scientific World Journal, 2012 Diamond-Blackfan anemia (DBA) is a congenital erythroid hypoplastic anemia, characterized by macrocytic anemia, reticulocytopenia, and severely reduced numbers of erythroid precursors in the bone marrow.
Sara E. Sjögren, Johan Flygare
doaj +1 more source
Pure Red Cell Aplasia with Del(20q) Sensitive for Immunosuppressive Treatment
Case Reports in Hematology, 2020 Pure red cell aplasia (PRCA) is a rare syndrome that only affects the erythroid lineage. It is defined by a normocytic, normochromic anemia with a marked reticulocytopenia and severe reduction or absence of erythroid precursors in the bone marrow ...
Anh Khoi Vo +5 more
doaj +1 more source