A five year review of clinical profile in HSP

N Grover1, N Sankhyan, J P Bisht

  • 1Dept. of Pediatrics, Indira Gandhi Medical College, Shimla, Himachal Pradesh, India. drngrover@rediffmail.com

Insights

Henoch-Schönlein Purpura (HSP) commonly affects children, primarily involving skin, joints, and the gastrointestinal tract. Early recognition of classic symptoms is key, though atypical presentations can cause diagnostic challenges.

Area of Science:

  • Pediatrics
  • Rheumatology
  • Nephrology

Background:

  • Henoch-Schönlein Purpura (HSP) is a common vasculitis affecting small blood vessels.
  • Understanding its clinical profile in children is crucial for timely diagnosis and management.

Observation:

  • A retrospective case series reviewed 30 children diagnosed with HSP.
  • Focus was placed on clinical manifestations, including skin, joint, gastrointestinal (GIT), and renal involvement.
  • Two cases with unusual features were detailed.

Findings:

  • All patients (100%) exhibited skin involvement, predominantly palpable purpura.
  • Joint (86.7%), GIT (80%), and renal (30%) systems were also frequently affected.
  • Abdominal pain and arthritis (knee/ankle) were common; atypical presentations like vesciculobullous lesions occurred.

Implications:

  • Most children present with classical HSP manifestations.
  • Atypical or absent cutaneous features at onset can lead to diagnostic confusion.
  • Awareness of diverse clinical profiles aids in accurate pediatric HSP diagnosis.