Borlu Murat, Ukşal Umit, Ferahbaş Ayten, Evereklioglu Cem
Department of Dermatology, Erciyes University Medical Faculty, Kayseri, Turkey.
Int J Dermatol. 2006 Jun;45(6):713-6. doi: 10.1111/j.1365-4632.2006.02754.x.
Behçet's disease (BD) is a systemic inflammatory vasculitis of young adults with unknown etiology.
The aim of this study was to determine the clinical features and outcome of BD in childhood.
Seventeen patients with BD within a pediatric age group were studied since 1997.
Boys : girls ratio was 12:5. Familial cases were very frequent (45%). Oral aphthous ulcers were present in all patients (100%), genital aphthous ulcers were present in 16 (94%), ocular lesions in 4 (24%), erythema nodosum in 3 (18%), papulopustules in 8 (47%), joint symptoms in 13 (76%), mild gastrointestinal symptoms in 2 (12%), neurological involvement in 2 (12%), positive pathergy reactions in 13 (76%), and thrombophlebitis in 1 (6%). We used colchicine, systemic corticosteroids, cyclosporine, nonsteroidal anti-inflammatory drugs, sulfasalazine, and topical agents for the treatment of children with BD.
The findings of BD in children are similar as in adults, but the frequency of familial cases is significantly higher.
白塞病(BD)是一种病因不明的年轻成年人系统性炎症性血管炎。
本研究旨在确定儿童白塞病的临床特征和预后。
自1997年起对17例儿科年龄组的白塞病患者进行了研究。
男童与女童比例为12:5。家族性病例非常常见(45%)。所有患者均有口腔阿弗他溃疡(100%),16例有生殖器阿弗他溃疡(94%),4例有眼部病变(24%),3例有结节性红斑(18%),8例有丘疹脓疱(47%),13例有关节症状(76%),2例有轻度胃肠道症状(12%),2例有神经受累(12%),13例有阳性针刺反应(76%),1例有血栓性静脉炎(6%)。我们使用秋水仙碱、全身性皮质类固醇、环孢素、非甾体抗炎药、柳氮磺胺吡啶和局部用药治疗儿童白塞病。
儿童白塞病的表现与成人相似,但家族性病例的发生率明显更高。