Henoch-Schonlein purpura
Revisión del 19:32 7 jun 2011 de Rossdonaldson1 (discusión | contribs.)
Background
-HSP, aka anaphylactoid purpura
-systemic vasculitis associated with abdominal pain and rash
-usually age 4-11, may occur in adults
-commonly occurs in springtime after viral URI
Diagnosis
-clinical diagnosis based on presence of abdominal pain, classic rash, microscopic hematuria, arthralgias in otherwise well appearing child
-symptoms: abdominal pain, nausea, vomiting, diarrhea, rash, mild arthralgias
-rash: palpable purpura on buttocks and lower extremities
-intussusception: ileoileal more common than ileocolic inpatients with HSP
Work-Up
- CBC, Chem7
- UA
- Blood cx
- ESR
- consider CT abdomen (ileoileal intussusception difficult to detect by US)
DDx
- meningococcemia (febrile, ill appearing)
- erythema nodosum
Treatment
- dz self limited: 94% recover completely
- consider corticosteroids for severe disease (abdominal pain, hematuria, arthralgias)
- prednisone 1mg/kg/day
Disposition
- most patients managed safely as outpatient
- consider admission for:
- uncertain diagnosis to exclude possibility of meningococcemia
- severe abdominal pain and vomiting
Source
Adapted from Rosens 7th edition
