Difficult-to-treat Takayasu arteritis: a case-based review.
Nabil Belfeki1, Nouha Ghriss2, Renaud Guedec-Ghelfi3
1Department of Internal Medicine and Clinical Immunology, Groupe Hospitalier Sud Ile de France, Melun, France. nabil.belfeki@ghsif.fr.
Rheumatology International
|October 23, 2024
Summary
Takayasu arteritis management is challenging. A refractory case achieved remission with a novel multitarget therapy combining infliximab, Upadacitinib, and methotrexate.
Area of Science:
- Rheumatology
- Immunology
- Internal Medicine
Background:
- Takayasu arteritis is a rare, chronic, large vessel vasculitis affecting the aorta and its branches.
- Diagnosis relies on the 2022 ACR/EULAR classification criteria.
- Management is challenging due to frequent relapses and disease progression despite corticosteroid treatment.
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