(D86.8) Sarcoidosis of other and combined sites

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1 411 941 in individuals diagnosis sarcoidosis of other and combined sites confirmed
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20 415 deaths with diagnosis sarcoidosis of other and combined sites
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1% mortality rate associated with the disease sarcoidosis of other and combined sites

Diagnosis sarcoidosis of other and combined sites is diagnosed Women are 0.03% more likely than Men

705 793

Men receive the diagnosis sarcoidosis of other and combined sites

9 429 (1.3 %)

Died from this diagnosis.

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706 148

Women receive the diagnosis sarcoidosis of other and combined sites

10 986 (1.6 %)

Died from this diagnosis.

Risk Group for the Disease sarcoidosis of other and combined sites - Men aged 30-34 and Women aged 50-54

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In Men diagnosis is most often set at age 5-89
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Less common in men the disease occurs at Age 0-5, 90-95+Less common in women the disease occurs at Age 0-5, 95+
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In Women diagnosis is most often set at age 5-94

Disease Features sarcoidosis of other and combined sites

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Absence or low individual and public risk
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Sarcoidosis of other and combined sites - what does this mean

Sarcoidosis of other and combined sites is a chronic inflammatory disease that can affect any organ or tissue in the body. it is characterized by the formation of granulomas, which are small collections of inflammatory cells. the cause of the disease is not known, however, it is believed to be related to an abnormal immune response to a trigger such as an infection or environmental exposure. symptoms vary depending on the organ or tissue affected.

What happens during the disease - sarcoidosis of other and combined sites

Sarcoidosis of other and combined sites is a rare inflammatory disorder that can affect multiple organs and tissues throughout the body. it is believed to be caused by an abnormal immune response to an unknown environmental trigger, resulting in the formation of granulomas in the affected organs or tissues. these granulomas cause inflammation and can lead to the development of scar tissue, which can cause organ dysfunction or tissue damage. in some cases, the inflammation can cause the release of cytokines, which can further worsen the symptoms.

Clinical Pattern

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How does a doctor diagnose

  • Physical examination
  • Chest X-ray
  • CT scan of chest
  • Pulmonary function tests
  • Bronchoscopy
  • Sputum cytology
  • Lung biopsy
  • Skin biopsy
  • Blood tests
  • Urine tests
  • MRI scan
  • Gallium scan

Treatment and Medical Assistance

Main Goal: To reduce inflammation and prevent the worsening of symptoms.
  • Prescribe corticosteroids to reduce inflammation.
  • Administer immunosuppressive drugs to suppress the immune system.
  • Prescribe antibiotics to treat any infection.
  • Prescribe antifungal medications to treat any fungal infection.
  • Perform regular physical exams to monitor the condition.
  • Perform imaging tests such as X-rays or CT scans to monitor the progression of the disease.
  • Perform pulmonary function tests to measure the amount of oxygen in the blood and to assess the functioning of the lungs.
  • Refer the patient to a specialist for further evaluation and treatment.
  • Provide lifestyle advice such as quitting smoking and avoiding contact with substances that may irritate the lungs.
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12 Days of Hospitalization Required
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Average Time for Outpatient Care Not Established

Sarcoidosis of other and combined sites - Prevention

The best way to prevent sarcoidosis of other and combined sites is to practice good hygiene and avoid exposure to known risk factors such as environmental pollutants, certain medications, and certain infections. additionally, it is important to maintain a healthy lifestyle with a balanced diet, regular exercise, and adequate rest. vaccines and other preventative measures may be recommended depending on the individual's risk factors.