Microangiopathic Hemolytic Anemia
📋Overview
This condition represents a pathological process rather than a standalone disease, occurring when red blood cells undergo fragmentation as they traverse microvasculature obstructed by fibrin or platelet aggregates. It is often identified by the presence of schistocytes, or fragmented red blood cells, on a peripheral blood smear.
The presence of this type of anemia can indicate various underlying clinical states, including thrombotic thrombocytopenic purpura, hemolytic uremic syndrome, or disseminated intravascular coagulation. Clinical management typically focuses on identifying the specific primary disorder responsible for the microvascular damage.
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Additional Resources
Medical codes (for reference)
UMLS CUI: C0221021Codes are provided for reference and interoperability. They are not a diagnosis.
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