Hemosiderinuria

From WikiMD's Wellness Encyclopedia

Hemosiderinuria is a medical condition characterized by the presence of hemosiderin in the urine. This condition is often associated with hemolytic anemia, intravascular hemolysis, and paroxysmal nocturnal hemoglobinuria.

Overview[edit | edit source]

Hemosiderinuria is a condition that is often associated with various forms of anemia, particularly hemolytic anemia. It is characterized by the presence of hemosiderin, a form of iron-storage complex, in the urine. This condition is often a sign of excessive intravascular hemolysis, where red blood cells are destroyed in the bloodstream, releasing hemoglobin, which is then converted into hemosiderin.

Causes[edit | edit source]

Hemosiderinuria is often caused by conditions that lead to excessive intravascular hemolysis. These conditions can include:

  • Hemolytic anemia: This is a condition where the body destroys red blood cells faster than it can produce them.
  • Paroxysmal nocturnal hemoglobinuria: This is a rare disorder that causes red blood cells to break down earlier than normal.
  • Sickle cell anemia: This is a genetic disorder that leads to the production of abnormal hemoglobin, causing red blood cells to break down.

Symptoms[edit | edit source]

The primary symptom of hemosiderinuria is the presence of hemosiderin in the urine, which can lead to the urine appearing dark or bloody. Other symptoms can depend on the underlying cause of the condition and can include fatigue, shortness of breath, and rapid heart rate.

Diagnosis[edit | edit source]

Diagnosis of hemosiderinuria typically involves a urine test to detect the presence of hemosiderin. Additional tests may be performed to determine the underlying cause of the condition.

Treatment[edit | edit source]

Treatment for hemosiderinuria typically involves treating the underlying cause of the condition. This can involve medication, blood transfusions, or in some cases, a bone marrow transplant.

See Also[edit | edit source]

Hemosiderinuria Resources
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Contributors: Prab R. Tumpati, MD