Questions discussed in this category
This question is part of our collaboration with ACR Convergence 2024 to Continue the Conversation from the meeeting. This question was inspi...
Would you view this as a sign that disease is not adequately controlled despite labs and imaging suggesting no active vasculitis?
Do you monitor patients with CTAs or MRAs?
Can nodular scleritis be a presenting manifestation of GCA?
Would you push for biopsy before deciding on treatment?
Patient is with past history of glomerulonephritis in remission after rituximab for the past 2 years. +MPO/P-ANCA
Is there a role in temporal artery biopsy?
The patient is on mesalamine for Crohn’s and CellCept and HCQ for skin manifestations (currently on hold during workup). The infectious workup i...
This question is part of a collaboration with RheumMadness and is in reference to Pathogenic ANCA (RAVE Trial).
The patient has not responded/has contraindications to apremilast, colchicine, and adalimumab. When they were off azathioprine for 5 days in the past,...
And when do you consider (if ever) IGRT?
Per 2021 GCA Vasculitis Guidelines: low evidence, but conditional recommendation for CTA neck, chest, abd/pelvis. Is anybody following this or do you ...
Patient is asymptomatic. Labs showed +P-ANCA 1:160. Negative MPO and PR3.
MPO/PR3, P-ANCA negative. IgG4 normal.
What are your primary and secondary agents?
Would you obtain imaging? If so, what type of imaging?
In your experience, are there specific disease manifestations in which HLAB51 is particularly helpful?
Other than inflammatory markers and following symptoms/exam, do you need any other specific monitoring for progression to systemic disease?
How does this vary from continued disease monitoring?
Additionally, what is the current role for temporal artery ultrasound in workup for GCA?
Do you obtain vascular imaging routinely in these cases, and if so, do you use cross-sectional or invasive angiography?
Thoughts on sarilumab vs methotrexate, or just treat with steroids alone
There are multiple difficulties that could be seen: steroids can precipitate a sickle cell crisis, vasculitis and sickle cell can produce similar clin...
What if the patient has MGUS?
Do patients with type 1 cryoglobulins need a bone marrow biopsy as part of the work up?
How would you label such a patient?
Would you treat differently if they have poor functional status?
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