This site is intended for healthcare professionals

Go to /sign-in page

You can view 5 more pages before signing in

Allergic cutaneous vasculitis

Last reviewed dd mmm yyyy. Last edited dd mmm yyyy

Authoring team

Leucocytoclastic vasculitis is a small vessel inflammatory disease mediated mostly by deposition of immune complexes.

  • seek dermatological advice
  • infections, medications, chemicals, bacteria, viruses, and diseases associated with immune complexes have been accused in the pathogenesis
  • may occur as an isolated cutaneous leucocytoclastic vasculitis that presents as palpable purpura most often localized in the lower extremities; if the condition is not isolated then other symptoms may occur such as abdominal pain, arthralgia and renal involvement (1)
  • comparatively common condition - accounts for approximately 50% of all cases of cutaneous vasculitis with the remainder having some sort of extracutaneous disease (2)
  • the clinical diagnosis of leucocytoclastic vasculitis is confirmed histopathologically by skin biopsy
  • in order to determine the cause of the disease, depending on the patient's history, various investigations may be indicated - complete blood cell count, blood cultures, cryoglobulins, serum protein electrophoresis, rheumatoid factor, antinuclear antibody, and autoantibodies to neutrophilic cytoplasmic antigens and complement
    • usually, ANCA and other autoantibodies are not present, and, if detected, the diagnosis of skin-limited disease should then only be made after rigorously excluding the possibility of systemic vasculitis (2)
  • once the diagnosis of leucocytoclastic vasculitis is made, emphasis should be on the search for an aetiological factor and the identification of the involved organs
  • if possible, the underlying cause should be treated or removed, for example discontinuation of drugs
  • prognosis depends on the disease that has the cutaneous leucocytoclastic angiitis as a component, as well as the severity of internal organ involvement. For example, a patient with cutaneous leucocytoclastic angiitis and moderate nephritis as component of Henoch-Schonlein purpura has a much better prognosis than a patient with these same findings as a component of Wegener's granulomatosis

Reference:


Related pages

Create an account to add page annotations

Add information to this page that would be handy to have on hand during a consultation, such as a web address or phone number. This information will always be displayed when you visit this page

The content herein is provided for informational purposes and does not replace the need to apply professional clinical judgement when diagnosing or treating any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions.

Connect

Copyright 2024 Oxbridge Solutions Limited, a subsidiary of OmniaMed Communications Limited. All rights reserved. Any distribution or duplication of the information contained herein is strictly prohibited. Oxbridge Solutions receives funding from advertising but maintains editorial independence.