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Case Report: Acute hemorrhagic edema of infancy (Seidlmayer purpura) - a dramatic presentation for a benign disease.
Carboni, Elena; Scavone, Maria; Stefanelli, Ettore; Talarico, Valentina; Zampogna, Stefania; Galati, Maria Concetta; Raiola, Giuseppe.
Afiliación
  • Carboni E; Department of Pediatrics, Magna Graecia University of Catanzaro, Catanzaro, Italy.
  • Scavone M; Department of Pediatrics, Magna Graecia University of Catanzaro, Catanzaro, Italy.
  • Stefanelli E; Department of Pediatrics, Magna Graecia University of Catanzaro, Catanzaro, Italy.
  • Talarico V; Department of Pediatrics, Pugliese Ciaccio Hospital, Catanzaro, Italy.
  • Zampogna S; Department of Pediatrics, Pugliese Ciaccio Hospital, Catanzaro, Italy.
  • Galati MC; Department of Pediatric Oncology and Hematology, Pugliese Ciaccio Hospital, Catanzaro, Italy.
  • Raiola G; Department of Pediatrics, Pugliese Ciaccio Hospital, Catanzaro, Italy.
F1000Res ; 8: 1771, 2019.
Article en En | MEDLINE | ID: mdl-31942241
ABSTRACT
We present a case of an 11-month-old girl who was referred to our unit for an erythematous rash that appeared on the face and extremities. Personal and family history was not relevant. Laboratory tests were normal. During recovery, diameter and colour intensity of the cutaneous lesions increased, but after some weeks, lesions had a self-limited resolution without any treatment. Based on clinical and laboratory findings, a diagnosis of acute hemorrhagic edema of infancy (AHEI) was made.  AHEI is a rare cutaneous leukocytoclastic vasculitis that usually affects children aged between 4 and 24 months. Etiology is unknown but almost of 75% of cases are preceded by infectious episodes, vaccinations or use of medications. In contrast to the dramatic cutaneous eruption, clinical conditions are usually optimal. Classically, AHEI is characterized by a triad of symptoms fever, edema and purpura. Skin lesions are erythematous, annular, medallion-like, purpuric plaques that have a rapid onset and appear on the face and extremities, sparing trunk and mucosal membranes. Initially interpreted as a variant of Henoch-Schönlein purpura, now it is considered a distinct disease. In the majority of cases the disease is benign and self-limited without a visceral involvement, so a conservative approach is most often chosen.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Púrpura / Vasculitis Leucocitoclástica Cutánea Tipo de estudio: Diagnostic_studies Límite: Female / Humans / Infant Idioma: En Revista: F1000Res Año: 2019 Tipo del documento: Article País de afiliación: Italia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Púrpura / Vasculitis Leucocitoclástica Cutánea Tipo de estudio: Diagnostic_studies Límite: Female / Humans / Infant Idioma: En Revista: F1000Res Año: 2019 Tipo del documento: Article País de afiliación: Italia