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Immunoglobulin A vasculitis in Infant/Neonate
Other Resources UpToDate PubMed

Immunoglobulin A vasculitis in Infant/Neonate

Contributors: Yun Xue MD, Susan Burgin MD
Other Resources UpToDate PubMed

Synopsis

Immunoglobulin A vasculitis (IgAV), formerly called Henoch-Schönlein purpura, is a necrotizing small-vessel vasculitis of unknown etiology that is the most common form of vasculitis in children aged younger than 10 years. It is characterized by IgA-immune complex and C3 and fibrin deposition in small vessels: primarily capillaries, postcapillary venules, and occasionally arterioles in affected organs. The annual incidence in childhood is 3-26 per 100 000. It is seen more frequently in males, White individuals, and those of Asian descent, commonly during fall and winter seasons. Episodes can often be preceded by an upper respiratory infection.

IgAV is characterized clinically by palpable purpura, abdominal pain, arthritis, and hematuria. Children are more likely to have fevers and abdominal pain. There are prodromal symptoms of malaise, headache, and arthralgias. An individual episode may persist for 3-6 weeks, with recurrences in many patients.

Almost all patients develop palpable purpura. Other skin involvement may include petechiae, bullae, edema, and necrosis. Infants' skin involvement is sometimes limited to the face or arms. Joint abnormalities are the second most common symptom and may accompany skin eruptions with severe pain and sometimes swelling, warmth, and tenderness. Ankles and knees are most often involved; symptoms are often transient and migratory.

Severe abdominal pain, vomiting, hematemesis, diarrhea, and hematochezia occur in about 50% of children. An involved inflamed and edematous bowel may be accompanied by appendicitis, ileus, and infarction. Intussusception and bowel perforation are more common in children than in adults.

Renal involvement occurs in 20%-50% of children and is usually self-limited, with only 1%-3% of patients progressing to end-stage renal disease. Risk factors for more severe renal disease include increased age at presentation, increased levels of serum IgA, and baseline nephritic or nephrotic disease. Notably, skin lesions above the waist may indicate higher risk in adults, but studies have not shown this in children.

Codes

ICD10CM:
D69.0 – Allergic purpura

SNOMEDCT:
191306005 – Henoch-Schönlein purpura

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Last Updated:09/27/2022
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Immunoglobulin A vasculitis in Infant/Neonate
A medical illustration showing key findings of Immunoglobulin A vasculitis : Abdominal pain, Diarrhea, Vomiting, Buttocks, Extensor distribution, Hand edema, Hematuria, Palpable purpura, Symmetric extremities distribution, Arthralgia, Foot edema, ESR elevated, Legs
Clinical image of Immunoglobulin A vasculitis - imageId=45124. Click to open in gallery.  caption: 'A close-up of many purpuric macules and papules, some with central vesiculation.'
A close-up of many purpuric macules and papules, some with central vesiculation.
Copyright © 2024 VisualDx®. All rights reserved.