Paroxysmal Nocturnal Hemoglobinuria (PNH)

Paroxysmal nocturnal hemoglobinuria

Paroxysmal
Paroxysmal nocturnal hemoglobinuria (PNH), sometimes referred to as Marchiafava-Micheli syndrome, is a rare, acquired, potentially life-threatening disease of the blood characterised by complement-induced intravascular hemolytic anemia (anemia due to destruction of red blood cells in the bloodstream), red urine (due to the appearance of hemoglobin in the urine) and thrombosis. PNH is the only hemolytic anemia caused by an acquired (rather than inherited) intrinsic defect in the cell membrane (deficiency of glycophosphatidylinositol leading to absence of protective proteins on the membrane)...

Paroxysmal Nocturnal Hemoglobinuria (PNH) - List of case studies

Pancytopenia of uncertain pathogenesis

the patient should be evaluated for the possibility of paroxysmal nocturnal hemoglobinuria with flow cytometries looking for the absence of CD55 ...

Massive Portal and Mesenteric Vein Thrombosis

Still not excluded - myeloproliferative syndromes and Paroxysmal Nocturnal Hemoglobinuria (PNH). - Abdominal inflammation – ...

Symptomatic Pancytopenia- Additional opinion

possibility in a patient with hypocellular marrow is paroxysmal nocturnal hemoglobinuria (PNH). In any case, one has to exclude the ...

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