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[PFAPA syndrome - An important differential diagnosis in children with recurrent fever]. / PFAPA-syndrom ­ en viktig differential­diagnos hos barn med återkommande feberepisoder.
Rydenman, Karin; Berg, Stefan; Karlsson-Bengtsson, Anna; Fasth, Anders; Wekell, Per.
Affiliation
  • Rydenman K; NU-sjukvården - Barn- och ungdomskliniken Uddevalla, Sweden NU-sjukvården - Barn- och ungdomskliniken Uddevalla, Sweden.
  • Berg S; Institutionen för kliniska vetenskaper, Sahlgrenska Akademin, Göteborgs Universitet - Avdelningen för pediatrik Göteborg, Sweden Institutionen för kliniska vetenskaper, Sahlgrenska Akademin, Göteborgs Universitet - Avdelningen för pediatrik Göteborg, Sweden.
  • Karlsson-Bengtsson A; Avdelningen för reumatologi och inflammationsforskning, Institutionen för medicin, Sahlgrenska akademin, Göteborgs universitet - Göteborg, Sweden Institutionen för medicin, Sahlgrenska akademin, Göteborgs Universitet. - Avdelningen för reumatologi och inflammationsforskning Göteborg, Sweden.
  • Fasth A; Drottning Silvias barn- och ungdomssjukhus - Göteborg, Sweden Goteborgs universitet Sahlgrenska Akademin - pediatrik Goteborg, Sweden.
  • Wekell P; NU-sjukvården - Barn- och ungdomskliniken Uddevalla, Sweden NU-sjukvården - Barn- och ungdomskliniken Uddevalla, Sweden.
Lakartidningen ; 1162019 Oct 29.
Article in Sv | MEDLINE | ID: mdl-31661147
Periodic Fever, Aphthous Stomatitis, Pharyngitis and Cervical Adenitis (PFAPA) syndrome is the most common autoinflammatory disorder among children in many parts of the world and an important differential diagnosis in children presenting with recurrent fever episodes. Commonly, PFAPA has an onset under the age of 5 years. Fever episodes in PFAPA usually last 3-6 days and are associated with one or more of the cardinal symptoms aphthous stomatitis, pharyngitis and cervical adenitis. The fever episodes typically recur with an interval of 3-6 weeks, often with a striking regularity. During the episodes, the patient has elevated inflammatory variables such as CRP and serum amyloid A (SAA) and may sometimes have additional symptoms such as abdominal pain, nausea and leg pain. Between the fever episodes, the patient is typically free of symptoms with normalized inflammatory variables and grows normally. Awareness and recognition of PFAPA is key to providing the patient with adequate treatment and avoiding misdiagnosis.
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Hereditary Autoinflammatory Diseases Type of study: Diagnostic_studies / Etiology_studies Limits: Child, preschool / Female / Humans / Male Language: Sv Journal: Lakartidningen Year: 2019 Document type: Article Affiliation country: Sweden Country of publication: Sweden
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Collection: 01-internacional Database: MEDLINE Main subject: Hereditary Autoinflammatory Diseases Type of study: Diagnostic_studies / Etiology_studies Limits: Child, preschool / Female / Humans / Male Language: Sv Journal: Lakartidningen Year: 2019 Document type: Article Affiliation country: Sweden Country of publication: Sweden