Erratum

Sep 16, 2017 by in HEMATOLOGY Comments Off on Erratum

In the April 2014 issue (Volume 28, number 2), in the article “The Role of Adenosine Signaling in Sickle Cell Therapeutics,” a potential conflict of interest for co-author Joel Linden…

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Bladder Cancer

Sep 16, 2017 by in HEMATOLOGY Comments Off on Bladder Cancer

Joaquim Bellmunt, MD, PhD, Editor After very little advancement in the last two decades, bladder cancer is back in the spotlight with the advent of new immunotherapy approaches and the…

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Current and Future Pharmacologic Complement Inhibitors

Sep 16, 2017 by in HEMATOLOGY Comments Off on Current and Future Pharmacologic Complement Inhibitors

The availability of anticomplement therapies has been a major achievement for medicine in the last decade. Indeed, eculizumab has changed the treatment paradigm of paroxysmal nocturnal hemoglobinuria and atypical hemolytic…

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Thrombotic Microangiopathy

Sep 16, 2017 by in HEMATOLOGY Comments Off on Thrombotic Microangiopathy

Thrombotic microangiopathies (TMA) such as atypical hemolytic uremic syndrome (aHUS) have evolved from rare, fulminant childhood afflictions to uncommon diseases with acute and chronic phases involving both children and adults….

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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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