Human parvovirus B19 (PV-B19) causes erythema infectiosum, hydrops fetalis, and transient aplastic crisis in immunocompromised patients with chronic hemolytic anemia, arthralgia, and chronic pure red cell aplasia [1]. It may also cause autoimmune hemolytic anemia [2] (which presents as aplastic crisis with reticulocytopenia or increased erythropoiesis with reticulocytosis) [3], autoimmune throm...

common itl hemolytic anemia. In a case described by Baty,’ the reticulocytes numbered 92 per cent. There is no completely satisfactory explanation of the nature of hemolytic crisis, nor of the mechanisms responsible for the recovery phenomenon. Lepel2 and Dameshek and Schw-art.z3 pointed out the similarity betw-eetl the various phenomena observed in the hemolytic anemia of humans w-ith those ob...

Pernicious anemia is an autoimmune disease with a variety of clinical presentations. We describe a case of pernicious anemia presenting with pancytopenia with hemolytic features. Further workup revealed very low vitamin B12 levels and elevated methylmalonic acid. It is important for a general internist to identify pernicious anemia as one of the cause of pancytopenia and hemolytic anemia to avo...

INTRODUCTION Sickle cell anemia and thalassemia result in impaired bone health in both adults and youths. Children with other types of chronic hemolytic anemia may also display impaired bone health. STUDY DESIGN To assess bone health in pediatric patients with chronic hemolytic anemia, a cross-sectional study was conducted involving 45 patients with different forms of hemolytic anemia (i.e., ...

BACKGROUND Interleukin-17A is the signature cytokine of the Th17 subset and drives inflammatory pathology, but its relevance to autoantibody-mediated diseases is unclear. Th1 cells secreting interferon-γ have been implicated in autoimmune hemolytic anemia, so the aim was to determine which cytokine is more closely associated with disease severity. DESIGN AND METHODS Interferon-γ and interleuk...

Hemolytic uremic syndrome (HUS) is a thrombotic microangiopathy defined by the triad of sudden onset hemolytic anemia, thrombocytopenia, and acute kidney injury. We describe rare case atypical HUS secondary to pancreatitis with an unknown etiology in 20-year-old male who presented complaint nausea, vomiting, abdominal pain.

By Bm N S. Bin L AND IRvIN N. KUHN A FORM OF HEMOLYTIC ANEMIA characterized by thrombocytopenia and the presence of fragmented red cells in the peripheral blood has been called microangiopathic hemolytic anemia by Brain, Dacie and Hourihane.’ These workers showed that in this disease the amount of hemoglobinemia and the degree of erythrocyte fragmentation correlated closely with the severity of...

By Bm N S. Bin L AND IRvIN N. KUHN A FORM OF HEMOLYTIC ANEMIA characterized by thrombocytopenia and the presence of fragmented red cells in the peripheral blood has been called microangiopathic hemolytic anemia by Brain, Dacie and Hourihane.’ These workers showed that in this disease the amount of hemoglobinemia and the degree of erythrocyte fragmentation correlated closely with the severity of...

By Bm N S. Bin L AND IRvIN N. KUHN A FORM OF HEMOLYTIC ANEMIA characterized by thrombocytopenia and the presence of fragmented red cells in the peripheral blood has been called microangiopathic hemolytic anemia by Brain, Dacie and Hourihane.’ These workers showed that in this disease the amount of hemoglobinemia and the degree of erythrocyte fragmentation correlated closely with the severity of...

Successful Treatment of Refractory Autoimmune Hemolytic Anemia (AIHA) in a Child, Based on Iranian Traditional Medicine: A Case Report