Sickle-cell thalassemia, unspecified, with acute chest syndrome digital illustration

Sickle-cell thalassemia, unspecified, with acute chest syndrome Save


ICD-10 code: D57.411

Disease category: D57.41: Sickle-cell thalassemia with crisis

Sickle-cell Thalassemia, Unspecified, with Acute Chest Syndrome

Sickle-cell thalassemia is a genetic disorder that affects the production of hemoglobin, a protein in red blood cells that carries oxygen throughout the body. This disorder is caused by mutations in the genes that control the production of hemoglobin, resulting in the formation of abnormal hemoglobin molecules that can cause red blood cells to become misshapen and break down prematurely.

When sickle-cell thalassemia is combined with acute chest syndrome, the condition can become life-threatening. Acute chest syndrome is a serious complication of sickle cell disease that occurs when sickle-shaped red blood cells block the blood vessels in the lungs, leading to chest pain, shortness of breath, and difficulty breathing.

  1. Cause: Sickle-cell thalassemia is caused by mutations in the genes that control the production of hemoglobin.
  2. Symptoms: Symptoms of sickle-cell thalassemia with acute chest syndrome include chest pain, shortness of breath, difficulty breathing, fever, and cough.
  3. Diagnosis: A diagnosis of sickle-cell thalassemia is typically made through a blood test that detects the presence of abnormal hemoglobin molecules. Acute chest syndrome can be diagnosed through a physical exam, chest X-ray, and blood tests.
  4. Complications: Sickle-cell thalassemia with acute chest syndrome can lead to a number of complications, including lung damage, pulmonary hypertension, and stroke.

While there is currently no cure for sickle-cell thalassemia, treatment can help manage symptoms and prevent complications. Treatment options may include blood transfusions, medication to reduce pain and inflammation, and bone marrow transplant in some cases.

If you or someone you know is experiencing symptoms of sickle-cell thalassemia with acute chest syndrome, it is important to seek medical attention immediately. Early diagnosis and treatment can help prevent serious complications and improve overall quality of life.

Treatment of Sickle-cell thalassemia, unspecified, with acute chest syndrome:

Treatment Options for Sickle-Cell Thalassemia, Unspecified, with Acute Chest Syndrome
Sickle-cell thalassemia is a genetic blood disorder that affects the production of hemoglobin, the protein in red blood cells that carries oxygen throughout the body. Acute chest syndrome is a complication of sickle-cell disease that occurs when sickle-shaped red blood cells block blood vessels in th...

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