cutaneous small vessel vasculitis (LCV) Flashcards
Pathogenesis of LCV:
Antigen is bound by antibodies, forms immune complexes that deposit into post-capillary venues→ activation of complement→inflammation of vessels
Triggers of LCV:
MANIC:
Medications: beta lactams, bactrim, thiazides, OCPs
Autoimmune CTD: Lupus, RA, sjogren’s
NSAIDS
Infections and IBD: group A strep, hepatitis, HIV, candida
Cancer: leukemias and solid organ cancers
Clinical presentation of LCV:
petechiae and palpable purport on lower extremities that present 1-2 weeks after a trigger (or 6 months after autoimmune disease or cancer)
- may be itchy or painful or asymptomatic
How long after trigger does LCV typically present?
1-2 weeks, or 6 months for autoimmune or cancer trigger
What is the clinical course of LCV?
typically resolves over several weeks (but PIH can last for months to year)
Histology of LCV:
Lab workup for small vessel vasculitides:
if no concern for systemic involvement:
- CBC, BMP, ESR, LFTs, UA
If concern for systemic involvement:
- GI: stool guiaiac
- Renal: serial UAs
- Infectious: Hep panel, HIV
- Inflammatory: ESR/CRP, ANA, complement levels
- Neoplastic: SPEP/UPEP
What questions to ask to screen for systemic involvement in small vessel vasculitides?
do a full ROS!!!
- GI, renal, joints, fevers, myalgia, weight loss, infections