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(D76.3) Other histiocytosis syndromes
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80 032 in individuals diagnosis other histiocytosis syndromes confirmed
7 898 deaths with diagnosis other histiocytosis syndromes
10% mortality rate associated with the disease other histiocytosis syndromes
Diagnosis other histiocytosis syndromes is diagnosed Men are 32.15% more likely than Women
52 883
Men receive the diagnosis other histiocytosis syndromes
4 637 (8.8 %)Died from this diagnosis.
100
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27 149
Women receive the diagnosis other histiocytosis syndromes
3 261 (12.0 %)Died from this diagnosis.
Risk Group for the Disease other histiocytosis syndromes - Men and Women aged 0-5
In Men diagnosis is most often set at age 0-94
Less common in men the disease occurs at Age 95+Less common in women the disease occurs at Age 75-79, 85-95+
In Women diagnosis is most often set at age 0-74, 80-84
Disease Features other histiocytosis syndromes
Absence or low individual and public risk
Other histiocytosis syndromes - what does this mean
Other histiocytosis syndromes are a group of rare disorders characterized by an abnormal increase in the number of a type of white blood cell called histiocytes. these syndromes can cause a variety of symptoms depending on which organs are affected, and may include skin rashes, fever, joint pain, and organ damage.
What happens during the disease - other histiocytosis syndromes
Other histiocytosis syndromes is a group of disorders caused by the abnormal accumulation of histiocytes, a type of white blood cell, in various organs and tissues. this accumulation leads to inflammation and tissue damage, and can result in organ dysfunction, scarring, and other serious complications. the exact cause of other histiocytosis syndromes is unknown, but it is believed to be related to genetic and environmental factors. treatment for other histiocytosis syndromes typically involves immunosuppressive drugs, chemotherapy, and other supportive care measures.
Clinical Pattern
More details coming soon
How does a doctor diagnose
- Physical examination
- Laboratory tests, such as complete blood count, biochemical tests, and urinalysis
- Imaging studies, such as X-rays, CT scans, and MRI scans
- Biopsy of affected tissue
- Genetic testing
- Flow cytometry
- Immunophenotyping
- Cytogenetic analysis
Treatment and Medical Assistance
Main goal of the treatment: Treating Other Histiocytosis Syndromes
- Monitoring and managing symptoms and complications
- Medications to reduce inflammation and suppress the immune system
- Intravenous immunoglobulin therapy
- Radiation therapy
- Chemotherapy
- Stem cell transplantation
- Surgery
14 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Other histiocytosis syndromes - Prevention
Other histiocytosis syndromes can be prevented by avoiding exposure to environmental toxins, maintaining a healthy lifestyle, and avoiding contact with people who have a weakened immune system. additionally, it is important to get regular medical check-ups to monitor for any changes in health. vaccinations may also be recommended in some cases.