Results 131 to 140 of about 1,235 (149)
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Autoimmune Neutropenia, Hemolytic Anemia, and Reticulocytopenia in Hodgkin's Disease
Annals of Internal Medicine, 1984Excerpt Various immunologic abnormalities have been described in patients with Hodgkin's disease, including autoimmune hemolytic anemia and immune thrombocytopenia (1-3).
A B, Weitberg, D C, Harmon
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Reticulocytopenia in Sickle Cell Disease
American Journal of Diseases of Children, 1964Temporary failure of red cell production has been well documented in hematologically normal persons, usually in association with infection, allergy, or a toxin. 1,2 The brief duration of these episodes (seven to 14 days) in comparison to the relatively long life span of the normal erythrocyte (120 days) results in only a mild, transient, and usually ...
E, CHARNEY, G, MILLER
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Hepatosplenomegaly and Reticulocytopenia as Prominent Features of Atypical Hemolytic Uremic Syndrome
Pediatric Emergency Care, 2010This is a case of atypical hemolytic uremic syndrome (HUS) due to invasive pneumococcal disease in which the prominent clinical features were reticulocytopenia and hepatosplenomegaly, leading to the incorrect initial diagnosis of acute leukemia. Delayed diagnosis of HUS, especially in atypical cases, can lead to increased morbidity and mortality ...
Kirsten, Bechtel, Sandra, Iragorri
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Reticulocytopenia in severe autoimmune hemolytic anemia (AIHA) of the warm antibody type
Blut, 1983A patient with severe AIHA of the warm antibody type, absence of reticulocytes and red cell hyperplasia of the bone marrow is described. In order to maintain a reasonable hemoglobin level 38 units of washed packed red cells were required within 24 days. The treatment with high doses of steroids showed no permanent beneficial effect.
G, Hauke, A A, Fauser, S, Weber, D, Maas
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Transfusion, 2021
AbstractBackgroundHemolytic 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.Case DescriptionWe describe the case of a newborn with HDFN associated with an atypical immunoglobulin (Ig) G anti‐M that reacted best at
Lezlie H. Andersen +6 more
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AbstractBackgroundHemolytic 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.Case DescriptionWe describe the case of a newborn with HDFN associated with an atypical immunoglobulin (Ig) G anti‐M that reacted best at
Lezlie H. Andersen +6 more
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Transfusion, 1996
BACKGROUND: Autoantibodies with anti‐U specificity, usually in combination with autoantibodies of other specificities, have occasionally been identified in association with autoimmune hemolytic anemia. A case of life‐threatening autoimmune hemolytic anemia, characterized by several atypical features, including apparent intravascular hemolysis ...
G R, Roush +6 more
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BACKGROUND: Autoantibodies with anti‐U specificity, usually in combination with autoantibodies of other specificities, have occasionally been identified in association with autoimmune hemolytic anemia. A case of life‐threatening autoimmune hemolytic anemia, characterized by several atypical features, including apparent intravascular hemolysis ...
G R, Roush +6 more
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Transient reticulocytopenia in viral illness.
Annals of clinical and laboratory science, 1982Infection resulting in transient reticulocytopenia and anemia, the so called "aplastic crisis," has frequently been documented in patients with congenital hemolytic anemia. However, this association with hematologically normal patients has been less well recognized.
J J, Biemer, F M, Taylor
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Autoimmune hemolytic anemia with reticulocytopenia. A medical emergency.
JAMA, 1980In four cases of autoimmune hemolytic disease, rapidly developing anemia was associated with reticulocytopenia despite intensely erythroid bone marrow. Transfusions had been withheld because compatible blood could not be obtained, and each patient was virtually moribund on admission. Type-specific RBCs were administered promptly without reaction.
C L, Conley, S M, Lippman, P, Ness
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Beta thalassemia with reticulocytopenia: clinical, biochemical, and ultrastructural studies.
Blood cells, 1979An unusual form of beta thalassemia is described in two children of unrelated families. Its main features are a severe anaemia with a low reticulocyte count associated with an erythroblastic hyperplasia; these characteristics indicate a completely ineffective erythropoiesis. The results of the study of haemoglobin synthesis performed on the bone marrow
Y, Beuzard +5 more
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Parvovirus B19 infection associated with reticulocytopenia and chronic autoimmune hemolytic anemia.
The American journal of pediatric hematology/oncology, 1989A previously healthy 11-year-old white female presented with a Coomb's positive hemolytic anemia and reticulocytopenia. The patient was treated with prednisone (6.4 mg/kg/day) and had a stable hemoglobin with subsequent recovery of reticulocytes by 7 days. Bone marrow aspiration showed hypercellularity with arrest of red cell maturation.
M A, Smith, N S, Shah, J S, Lobel
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