Harper's Textbook of Pediatric Dermatology 2011
DOI: 10.1002/9781444345384.ch161
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Acute Haemorrhagic Oedema of the Skin in Infancy

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Cited by 8 publications
(13 citation statements)
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“…It is considered to be an immune complex‐mediated vasculitis and mostly affects infants between 4 months and 2 years of age (5). The aetiology is obscure, although it has been suggested that bacterial and viral infections (mainly of the upper respiratory and urinary tracts) contribute to the development of AHEI (6). The differential diagnosis includes urticarial vasculitis, Kawasaki disease, erythema multiforme, Sweet’s syndrome and Gianotti‐Crosti disease (7).…”
Section: The Case Presentation Can Be Found On Page 1390 Discussionmentioning
confidence: 99%
“…It is considered to be an immune complex‐mediated vasculitis and mostly affects infants between 4 months and 2 years of age (5). The aetiology is obscure, although it has been suggested that bacterial and viral infections (mainly of the upper respiratory and urinary tracts) contribute to the development of AHEI (6). The differential diagnosis includes urticarial vasculitis, Kawasaki disease, erythema multiforme, Sweet’s syndrome and Gianotti‐Crosti disease (7).…”
Section: The Case Presentation Can Be Found On Page 1390 Discussionmentioning
confidence: 99%
“…AHO of the skin was first described in an infant by Snow 1 in 1913, and useful reviews have been published recently 2–4 . The majority (80%) of cases occur in children aged < 2 years, and the condition has become known as ‘acute haemorrhagic oedema of infancy’, but cases have been reported in children up to the age of 60 months 3 …”
mentioning
confidence: 99%
“…Histology often, but not exclusively, shows leucocytoclastic vasculitis involving the small blood vessels of the dermis. Perivascular IgA deposits have been identified in about 30% of cases 4 …”
mentioning
confidence: 99%
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“…It was first described by Snow as a purely cutaneous variant of Henoch‐Schönlein purpura (1,2). Infants present with mild fever, edema of the face and extremities, erithemateous and purpuric lesions without systemic symptoms (1,3). Treatment is unnecessary.…”
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confidence: 99%