**Core Concept**
Paroxysmal nocturnal hemoglobinuria (PNH) is a rare acquired disorder characterized by the premature destruction of red blood cells, leading to hemolytic anemia. This condition arises due to a clonal expansion of hematopoietic stem cells with a mutation in the PIGA gene, resulting in the absence of glycosylphosphatidylinositol (GPI) anchors on the surface of blood cells.
**Why the Correct Answer is Right**
PNH is associated with the formation of blood clots, particularly in the hepatic and splenic veins, leading to thrombosis. The absence of GPI-anchored proteins, such as CD55 and CD59, on the surface of red blood cells makes them more susceptible to complement-mediated lysis. Additionally, PNH is linked to bone marrow failure, and patients may develop aplastic anemia or myelodysplastic syndrome.
**Why Each Wrong Option is Incorrect**
**Option A:** Bone marrow failure is a common complication of PNH, so this option is incorrect.
**Option B:** Thrombosis is a well-known complication of PNH, making this option incorrect as well.
**Option C:** Hemolytic anemia is a hallmark of PNH, so this option is also incorrect.
**Clinical Pearl / High-Yield Fact**
PNH should be considered in patients with unexplained hemolytic anemia, thrombocytopenia, or thrombosis, especially in the absence of other underlying causes.
**Correct Answer:** D
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