Hereditary Hemorrhagic Telangiectasia Type 4 C1857688
A hereditary condition causing abnormal blood vessel development similar to other HHT types. Results in nosebleeds, visible blood vessel spots, and possible organ involvement. Treatment addresses bleeding episodes and vascular lesions.
Key facts at a glance
- ICD-10
- Q24.9
- ICD-11
- LA00.0
- Body system
- cardiovascular
- Severity
- moderate
- Chronic
- true
Treatment options
Evidence-based approaches to managing this condition.
First-line treatments
Disease management and monitoring
Treatment options should be discussed with a qualified healthcare provider.
Systemic antifibrinolytic agents
Long-term tranexamic acid therapy to reduce bleeding frequency from mucocutaneous telangiectasias and visceral AVMs by inhibiting fibrinolysis at bleeding sites.
Endovascular embolization of AVMs
Transcatheter embolization of arteriovenous shunts in lungs, brain, or liver to eliminate right-to-left shunting and prevent paradoxical embolic complications.
Additional treatment options
Parenteral iron replacement therapy
Intravenous iron formulations for severe iron deficiency anemia secondary to chronic hemorrhage, when oral iron is inadequate or poorly tolerated.
medicationRadiofrequency ablation for telangiectasias
Application of radiofrequency energy to thermally destroy mucosal and cutaneous telangiectasias, reducing nosebleeds and skin bleeding in accessible areas.
procedureComprehensive HHT center surveillance program
Regular multidisciplinary follow-up including ENT, gastroenterology, pulmonology, and genetics to monitor for new AVM development and manage complications proactively.
monitoringMedication Comparisons
Compare medications used to treat Hereditary Hemorrhagic Telangiectasia Type 4 C1857688. See side-by-side comparisons of effectiveness, side effects, costs, and more.
View Medication ComparisonsThis information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 25, 2026. · Read our editorial policy