英文摘要 |
Henoch-Schönlein purpura (HSP), also known as anaphylactoid purpura, is the most common cause of vasculitis in children. HSP can affect multiple organs and is associated with a characteristic skin rash. Most cases resolve with symptomatic treatment, but serious complications such renal failure can occur. We present the case of a 7-year-old girl a 2-day history of arthralgia in the knees and ankles and polymorphic palpable skin purpura over the lower extremities. Laboratory data revealed a rising erythrocyte sedimentation rate, and the Mycoplasma pneumoniae antibody titer rose from 1:320 to >1:1280 within 10 days. Pathology evaluation of a skin biopsy revealed leukocytoclastic vasculitis, and HSP was diagnosed. The purpose of this report is to remind primary care physicians to be aware of this disease, since its incidence is frequently underestimated in primary care settings. A general practitioner should be able to recognize the manifestations of HSP, understand when to treat and when to refer, and be able to provide information to families about long-term consequences of HSP. |