Urticarial vasculitis in Adult
The lesions of urticarial vasculitis must be distinguished from those seen in acute and chronic urticaria. In contrast to the itch that predominates in acute and chronic urticaria, the plaques of urticarial vasculitis are often described as having a burning or painful sensation with mild itch. Additionally, each plaque in urticarial vasculitis persists for more than 24 hours and leaves behind residual hyperpigmented discoloration as it resolves. In contrast, each wheal of acute and chronic urticaria generally resolves within 24 hours and without residual discoloration.
Urticarial vasculitis is thought to represent a type III immune reaction with deposition of circulating immune complexes. It may be idiopathic in origin or may be precipitated by infections, medications, or neoplasms, and may be associated with connective tissue disease or paraproteinemia.
Complement levels in urticarial vasculitis may either be normal (normocomplementemic form) or low (hypocomplementemic form). While both forms can be associated with systemic symptoms including arthralgia (most common), the hypocomplementemic form is most commonly associated with more pronounced systemic involvement including pulmonary, ocular, gastrointestinal (GI), renal, and cardiac findings. Progressive chronic obstructive pulmonary disorder has been noted in hypocomplementemic urticarial vasculitis, particularly in smokers. There are also reports of bibasilar panacinar emphysema in these patients. Controversy exists as to the relationship between hypocomplementemic urticarial vasculitis and systemic lupus erythematosus (SLE), with some authors arguing that they are related disorders, or even potentially along one spectrum of disease.
Urticarial vasculitis can occur at any age, although it is most frequently noted in women in the fifth decade. It is rare in children; however, cases of both normocomplementemic and hypocomplementemic urticarial vasculitis have been reported. When hypocomplementemic urticarial vasculitis is seen in children, it is often associated with renal involvement.
Prognosis for urticarial vasculitis is generally noted to be positive, although outcomes largely depend on the presence of any associated or underlying disease. Rarely, marked renal involvement has been seen with hypocomplementemic urticarial vasculitis, more frequently in children than in adults. Additionally, there is one case report describing pulmonary hemorrhage in a child with urticarial vasculitis.
L95.9 – Vasculitis limited to the skin, unspecified
402656007 – Urticarial vasculitis
- Urticaria (acute versus chronic) – Transient urticarial lesions that last <24 hours and resolve without residual pigmentary changes. Lesions are characterized as acute urticaria when they occur for <6 weeks and chronic when they are of ≥6 weeks duration.
- Neutrophilic urticaria – Variant of urticaria that shows a neutrophilic infiltration on biopsy but no vasculitis.
- Serum sickness
- Systemic lupus erythematosus
- Cryopyrin-associated periodic syndromes (CAPS) – Familial cold autoinflammatory syndrome (FCAS), Muckle-Wells syndrome (MWS), and neonatal onset multisystem inflammatory disease (NOMID, also known as chronic infantile neurologic cutaneous and articular syndrome [CINCA])
- Schnitzler syndrome
- Cogan syndrome
- Mixed cryoglobulinemia
- Immunoglobulin A vasculitis (formerly Henoch-Schönlein purpura)
- Linear IgA dermatosis