Department of Pediatrics, Pontificia Universidad Católica de Chile, Lira 85, 5th floor, Santiago, Chile.
Clin Rheumatol. 2009 Oct;28(10):1235-7. doi: 10.1007/s10067-009-1222-z. Epub 2009 Jul 11.
PFAPA syndrome is characterized by episodes of periodic fever, aphthous stomatitis, pharyngitis, and cervical adenitis. PFAPA syndrome usually begins in children under 5 years old and normally has self-resolution. The etiology of PFAPA syndrome remains unknown. In this paper, we report the cases of two different families with siblings with PFAPA syndrome: two sisters and two brothers. To our knowledge, this is the first report of siblings with PFAPA syndrome.
PFAPA 综合征的特征为周期性发热、口疮性口炎、咽炎和颈淋巴结炎。PFAPA 综合征通常在 5 岁以下儿童中发病,通常可自行缓解。PFAPA 综合征的病因尚不清楚。本文报道了两户不同家庭的同胞兄妹均患 PFAPA 综合征的病例:两姐妹和两兄弟。据我们所知,这是首例 PFAPA 综合征同胞兄妹的报道。