Hemolytic anemia

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Hemolytic anemia
File:Modified sickle cell 01.jpg
Synonyms N/A
Pronounce N/A
Specialty N/A
Symptoms Fatigue, pallor, shortness of breath, jaundice, dark urine, splenomegaly
Complications Heart failure, arrhythmia, gallstones, leg ulcers
Onset Can be sudden or gradual
Duration Varies depending on cause
Types N/A
Causes Autoimmune disease, genetic disorders, infections, medications, toxins
Risks Family history, certain infections, autoimmune conditions
Diagnosis Complete blood count, reticulocyte count, Coombs test, bilirubin levels
Differential diagnosis Anemia of chronic disease, iron deficiency anemia, thalassemia
Prevention N/A
Treatment Depends on cause; may include corticosteroids, immunosuppressants, blood transfusion, splenectomy
Medication N/A
Prognosis Varies; some forms are chronic, others can be cured
Frequency Varies by type; some forms are rare, others more common
Deaths N/A


Hemolytic anemia is a condition in which red blood cells are destroyed and removed from the bloodstream before their normal lifespan is over. This destruction of red blood cells is called hemolysis. Hemolytic anemia can be either intrinsic or extrinsic.

Types[edit]

Hemolytic anemia can be classified into two main types:

Causes[edit]

The causes of hemolytic anemia can be diverse and include:

Symptoms[edit]

Common symptoms of hemolytic anemia include:

Diagnosis[edit]

Diagnosis of hemolytic anemia typically involves:

Treatment[edit]

Treatment of hemolytic anemia depends on the underlying cause and may include:

Prognosis[edit]

The prognosis of hemolytic anemia varies depending on the cause and severity of the condition. With appropriate treatment, many individuals can manage their symptoms and lead normal lives.

See also[edit]

References[edit]

External links[edit]


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