DISEASE SCANNER
Global Incurable Diseases Tracker
Takayasu Arteritis
A rare form of vasculitis affecting the large arteries, particularly the aorta and its main branches. Causes inflammation that damages arteries, leading to narrowing, blockage, or aneurysm formation. Affects mainly young women. Called 'pulseless disease'.
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Symptoms
Treatment Options
Risk Factors
Diagnostic Methods
- 1Physical examination (pulse deficit)
- 2Blood tests (ESR, CRP)
- 3CT angiography
- 4MRI/MRA
- 5PET scan
- 6Angiography
- 7Doppler ultrasound
Prognosis
Variable. 5-year survival >90% with treatment. Relapses common. Vascular complications significant. Hypertension management crucial. Pregnancy high-risk. Lifelong monitoring required.
Prevention
- No known prevention
- Early diagnosis
- Adequate treatment of inflammation
- Blood pressure control
- Smoking cessation
Research Status
Corticosteroids first-line. Immunosuppressants (methotrexate, azathioprine) for maintenance. Biologics (tocilizumab, rituximab) increasingly used. Vascular interventions for stenosis. Early diagnosis crucial to prevent complications.
Affected Countries
Sources
- https://www.mayoclinic.org/diseases-conditions/takayasus-arteritis
- https://www.hematology.org/education/patients
- https://www.ncbi.nlm.nih.gov/books
- https://rarediseases.org/rare-diseases
Medical Disclaimer
This information is for educational purposes only. Always consult healthcare professionals for medical advice, diagnosis, and treatment.