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NR Dec-03
Leukocytoclastic vasculitis
Habif, Thomas. Clinical dermatolog 3rd edition. 1996: 575-88.
Habit, Thomas. Skin disease: diagnosis and treatment 2001: 286-93.
Residents’ report with Dr. Kenneth Sack.
Key Points:
• Not all purpura is vasculitis
• Don’t forget drugs and neoplasms in your differential
• No need to send the whole work-up at once: focus based on history / physical, initial labs
and imaging
• Time may tell – follow for later development of systemic disease
Leukocytoclastic vasculitis
- Etiologies:
o Drugs (10%): penicillin, sulfa, allopurinol, thiazides, PTU, quinolones, retinoids, OTC; 721d after rx
o Infections: hepatitis, endocarditis
o Connective tissue disease: RA, SLE, Behcet’s, Wegener’s, PAN, HSP
o Neoplasms / paraneoplastic: CLL, lymphoma, Hodgkin’s, multiple myeloma
o Inflammatory bowel disease-associated
- DDx (other dermapathology mimicking leukocytoclastic vasculitis):
o Platelet: TTP, DIC
o Purpura fulminans
o Septic vasculitis
o Septic emboli
o Bacteremia
o Drug eruptions
o Rocky mountain spotted fever
o Scurvy
o Senile (traumatic purpura)
o Progressive pigmentary purpura (Schamberg’s – not associated with underlying disease)
- Pearls:
o History/physical:
ƒ Do the full ROS looking for rheumatologic / malignancy clues
ƒ Remember herbs and OTC medications
ƒ Look at the nail beds
o Rational work-up: start with basics, adding additional tests based on history and physical
ƒ Basic labs to start: CBC, renal panel, U/A, cultures, hepatitis serologies
ƒ Basic imaging: CXR
ƒ Limited value: ESR, cryoglobulins (limitations of test)
ƒ Other tests: increased diagnostic value if symptoms/signs point to disease (renal, GI,
etc)
o Age-appropriate cancer screening
o Dermatopathology: Tissue is the issue! Confirm your pathologic diagnosis.
ƒ Always ask for immunofluorescence!
o Time may tell: Not all symptoms / signs are present with initial vasculitis
ƒ Follow symptoms for natural course to diagnose underlying disease
ƒ Follow basic labs, including renal function / urinalysis