Chudwin D S, Daniels T E, Wara D W, Ammann A J, Barrett D J, Whitcher J P, Cowan M J
J Pediatr. 1981 Feb;98(2):213-7. doi: 10.1016/s0022-3476(81)80637-3.
Sjögren syndrome, consisting of keratoconjunctivitis sicca and xerostomia with or without another autoimmune disease, is uncommon in children. We describe our retrospective experience with eight pediatric patients with SS. All had recurrent parotid enlargement and abnormal salivary gland biopsies, six had keratoconjunctivitis sicca, and five had other autoimmune manifestations, although only two of these had other clearly defined autoimmune disorders (mixed connective tissue disease and hypergammaglobulinemic purpura). Our patients had a higher incidence of primary SS, parotid enlargement, and hematologic abnormalities than did children previously reported with SS. Children with SS demonstrate a clinical heterogeneity comparable to that seen in adults.
干燥综合征由干燥性角结膜炎和口干症组成,可伴有或不伴有其他自身免疫性疾病,在儿童中并不常见。我们描述了对8例儿童干燥综合征患者的回顾性研究经验。所有患者均有复发性腮腺肿大和唾液腺活检异常,6例有干燥性角结膜炎,5例有其他自身免疫表现,尽管其中只有2例有其他明确的自身免疫性疾病(混合性结缔组织病和高球蛋白血症性紫癜)。与先前报道的干燥综合征儿童相比,我们的患者原发性干燥综合征、腮腺肿大和血液学异常的发生率更高。患有干燥综合征的儿童表现出与成人相似的临床异质性。