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Normocomplementaemic Urticarial Vasculitis in a 19-Month-Old Girl
1Department of Anaesthesia and Pain Management, Royal Melbourne Hospital, Grattan Street, Parkville, VIC, Australia.
Insights
Urticarial vasculitis (UV), a rare condition, presented in a 19-month-old child with a distinctive rash. This case highlights the diagnostic challenges of pediatric UV.
Area of Science:
- Pediatrics
- Dermatology
- Immunology
Background:
- Urticaria is a common pediatric skin condition.
- Urticarial vasculitis (UV) is a rare, more severe variant.
- UV typically affects adults, with limited pediatric case reports.
Purpose of the Study:
- To report a case of urticarial vasculitis in a young child.
- To discuss the diagnostic and prognostic challenges of pediatric UV.
- To contribute to the limited literature on UV in infants.
Main Methods:
- Clinical presentation of a 19-month-old girl with a widespread rash.
- Physical examination revealing urticarial and palpable purpuric lesions.
- Laboratory investigations including complete blood count, electrolytes, renal function, coagulation profile, urinalysis, and erythrocyte sedimentation rate.
- Complement studies (including C1q) performed later.
Main Results:
- The patient presented with a widespread urticarial rash overlaid with palpable purpura and hyperpigmentation.
- Initial laboratory tests were largely normal, with a mildly elevated erythrocyte sedimentation rate.
- Complement studies, including C1q, were within normal limits.
- The patient was systemically well despite the extensive rash.
Conclusions:
- Pediatric urticarial vasculitis is rare and can present diagnostic challenges.
- The clinical presentation may mimic common urticaria, necessitating thorough investigation.
- Further research is needed to understand the unique aspects of UV in children.
Abstract:
Urticaria is common in children. Urticarial vasculitis (UV) is a potentially more serious, rare variant. The youngest reported case was 12 months of age. A systemically well, 19-month-old girl presented with her mother who was concerned about the development of a rash. On presentation, the child had normal vital signs, was alert, and was well and playing with toys. There was a widespread urticarial rash (raised, pruritic, and erythematous) that was most apparent on the trunk with minimal rash on the legs. Overlying this urticarial rash in a similar distribution was a blotchy, palpable purpuric rash and associated hyperpigmentation. Investigations revealed a normal level of haemoglobin, white cells, platelets, and electrolytes. Renal function, international normalised ratio, and activated partial thromboplastin time were all normal. There was no blood or protein in the urine. The erythrocyte sedimentation rate was mildly elevated at 19 mm/hour. Complement results (including C1q) obtained later were normal. This case is striking not only because of the rarity of UV in children but also due to the unique diagnostic and prognostic challenges that it raises.
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