03/01/2025
Presently Treating a case of HSP in a elderly Female with Skin , Joints, GI tract,lung involvement with Solumedrol Pulse therapy . Skin biopsy was supported HSP..
Henoch-Schönlein Purpura (HSP), now more commonly referred to as IgA vasculitis, is a type of small blood vessel inflammation (vasculitis) that primarily affects the skin, joints, gastrointestinal tract, and kidneys. It is most common in children but can occur at any age.
Key Features of HSP
1. Skin (Purpura):
• The hallmark of HSP is a purpuric rash, typically located on the lower extremities, especially on the buttocks and legs.
• The rash appears as small, red or purple spots caused by bleeding under the skin.
2. Joints (Arthritis or Arthralgia):
• Joint pain and swelling, often in the knees and ankles, are common but usually resolve without permanent damage.
3. Gastrointestinal Symptoms:
• Abdominal pain, nausea, vomiting, and blood in the stool may occur.
• Intestinal involvement can lead to complications like intussusception.
4. Kidneys (Renal Involvement):
• Hematuria (blood in the urine) and/or proteinuria (protein in the urine) may indicate kidney involvement, which can range from mild to severe (IgA nephropathy).
5. Other Symptoms:
• Rarely, HSP can affect the central nervous system, lungs, or sc***um (in males).
Causes and Pathophysiology
• Cause: The exact cause is unknown but is often triggered by an infection (commonly respiratory infections), medications, or other immune system triggers.
• Pathophysiology: Deposition of immune complexes containing IgA in small blood vessels leads to inflammation and tissue damage.
Diagnosis
HSP is a clinical diagnosis based on the characteristic symptoms, especially the presence of purpura in conjunction with other features. Tests may include:
• Blood Tests: To check for markers of inflammation (e.g., ESR, CRP) and rule out other causes.
• Urinalysis: To assess for hematuria and proteinuria.
• Skin or Kidney Biopsy: Rarely needed but may confirm IgA deposition.
Treatment
• Supportive Care: Most cases are self-limiting, requiring only symptomatic treatment such as hydration, pain management, and rest.
• Medications:
• NSAIDs for joint pain (if no kidney involvement).
• Corticosteroids for severe symptoms, such as significant abdominal pain, nephritis, or complications.
• Follow-Up: Monitoring for kidney involvement is essential, as renal issues may develop weeks to months after the initial onset.
Prognosis
• Most children recover fully without complications.
• Adults are more likely to experience severe kidney involvement, which can lead to long-term kidney issues.