General Internal Medicine
Questions discussed in this category
McCreary et al., PMID 37310038
Any particular concentration?
Hayashi et al., PMID 22272655
Ekstein et al., PMID 32905614
What changes do you make to your treatment approach to adapt to this altered disease state?
Would you view this as a sign that disease is not adequately controlled despite labs and imaging suggesting no active vasculitis?
When do you switch to steroid-sparing medications? What steroid-sparing therapies do you prefer?
And what workup do you pursue?
The patient is a young African American female of reproductive age with positive Fibrillarin antibody and nucleolar antibody. No ILD.
Is a BM biopsy a must when there is skin involvement?
If tryptase level is mildly elevated but less than 20 would you recommend a BM biopsy?
This question is part of a collaboration with RheumMadness and is in reference to Pathogenic ANCA (RAVE Trial).
How should IVIG and either biologic injections or infusions be spaced?
And if so, what is your approach to the diagnosis?
Do you typically start the patient on hydroxychloroquine?
What work-up do you perform?
How often do you order labs?
4 cutaneous biopsies with no evidence of vasculitis. Sjogren’s diagnosis based prominent sicca symptoms and a significantly elevated SSA.
For example, in the setting of cirrhosis incidentally found on imaging.
Should one restart lamotrigine or look for an alternative? If no other alternative available, is slow titration vs regular titration preferred?
Are there any medications that surgeons like discontinued before their procedure?
Does your evaluation hinge on nonresolution with warming? How extensive is your workup?
Does morphology guide your workup?
Especially in the setting of these being more narrow acting than tofacitinib, should we consider them safer than our old drugs?
Other than inflammatory markers and following symptoms/exam, do you need any other specific monitoring for progression to systemic disease?
Do you obtain vascular imaging routinely in these cases, and if so, do you use cross-sectional or invasive angiography?
What if the patient has MGUS?
Do patients with type 1 cryoglobulins need a bone marrow biopsy as part of the work up?
If so, are there specific patient populations for which you would use this metric?
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