HEMATOLOGY

Shiga Toxin Associated Hemolytic Uremic Syndrome

Sep 16, 2017 by in HEMATOLOGY Comments Off on Shiga Toxin Associated Hemolytic Uremic Syndrome

Shiga toxin associated hemolytic uremic syndrome (Stx HUS), a thrombotic microangiopathy, is the most common cause of pediatric acute kidney injury but has no direct treatment. A better understanding of…

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Congenital CD59 Deficiency

Sep 16, 2017 by in HEMATOLOGY Comments Off on Congenital CD59 Deficiency

The severe clinical symptoms of inherited CD59 deficiency confirm the importance of CD59 as essential complement regulatory protein for protection of cells against complement attack, in particular protection of hematopoietic…

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Paroxysmal Nocturnal Hemoglobinuria

Sep 16, 2017 by in HEMATOLOGY Comments Off on Paroxysmal Nocturnal Hemoglobinuria

Paroxysmal nocturnal hemoglobinuria is manifests with a chronic hemolytic anemia from uncontrolled complement activation, a propensity for thrombosis and marrow failure. The hemolysis is largely mediated by the alternative pathway…

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Paroxysmal Cold Hemoglobinuria

Sep 16, 2017 by in HEMATOLOGY Comments Off on Paroxysmal Cold Hemoglobinuria

Paroxysmal cold hemoglobinuria is a rare cause of autoimmune hemolytic anemia predominantly seen as an acute form in young children after viral illnesses and in a chronic form in some…

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Cold Agglutinin-Mediated Autoimmune Hemolytic Anemia

Sep 16, 2017 by in HEMATOLOGY Comments Off on Cold Agglutinin-Mediated Autoimmune Hemolytic Anemia

Cold antibody types account for about 25% of autoimmune hemolytic anemias. Primary chronic cold agglutinin disease (CAD) is characterized by a clonal lymphoproliferative disorder. Secondary cold agglutinin syndrome (CAS) complicates…

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Warm Autoimmune Hemolytic Anemia

Sep 16, 2017 by in HEMATOLOGY Comments Off on Warm Autoimmune Hemolytic Anemia

Warm autoimmune hemolytic anemia (AIHA) is defined as the destruction of circulating red blood cells (RBCs) in the setting of anti-RBC autoantibodies that optimally react at 37°C. The pathophysiology of…

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Hemolysis from ABO Incompatibility

Sep 16, 2017 by in HEMATOLOGY Comments Off on Hemolysis from ABO Incompatibility

ABO incompatibility of red blood cells leads to brisk complement-mediated lysis, particularly in the setting of red cell transfusion. The ABO blood group is the most clinically significant blood group…

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Complement

Sep 16, 2017 by in HEMATOLOGY Comments Off on Complement

The complement system is an essential component of the immune system. It is a highly integrative system and has a number of functions, including host defense, removal of injured cells…

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Complement in Health and Disease

Sep 16, 2017 by in HEMATOLOGY Comments Off on Complement in Health and Disease

Robert A. Brodsky, MD, Editor Related posts: Complement in Health and Disease Ultralarge Von Willebrand Factor–Induced Platelet Clumping and Activation of the Alternative Complement Pathway in Thrombotic Thrombocytopenic Purpura and…

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Novel Therapeutics for Pancreatic Adenocarcinoma

Sep 16, 2017 by in HEMATOLOGY Comments Off on Novel Therapeutics for Pancreatic Adenocarcinoma

The last decade has seen significant developments in the use of combination systemic therapy for advanced pancreatic ductal adenocarcinoma (PDAC), with median survival approaching 1 year for select patients treated with…

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