Alenazi Abdullatif, Al Sonbul Abdullah, Al Jumaah Suliman, Al Mehaidib Ali, Al-Mayouf Sulaiman M
Department of Pediatrics, Section of Rheumatology, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Ann Saudi Med. 2012 Jan-Feb;32(1):43-8. doi: 10.5144/0256-4947.2012.43.
Published data from Saudi Arabia regarding autoinflammatory diseases are scarce. In this study, we describe the clinical and laboratory features of autoinflammatory diseases in Saudi children.
Restrospective, hospital-based study conducted from January 2010 until June 2010.
Patients with autoinflammatory disease treated at the Pediatric Rheumatology Clinic at King Faisal Specialist Hospital and Research Center, Riyadh, over the past 10 years were included. Autoinflammatory diseases included the following: familial Mediterranean fever (FMF); chronic recurrent multifocal osteomyelitis (CRMO); early-onset sarcoidosis (EOS); periodic fever, aphthous stomatitis, pharyngitis and cervical adenitis syndrome (PFAPA); chronic infantile neurologic cutaneous and articular syndrome (CINCA); and Muckle-Wells syndrome (MWS). Demographic characteristics, diagnosis, age at onset, disease duration, follow-up duration, clinical and laboratory variables, and outcome data were compiled. Gathered laboratory data were part of patients' usual medical care.
Thirty-four patients (females, 53%) with autoinflammatory diseases were included (mean age, 151 months). Mean disease duration was 118 months; mean age at onset was 32 months; consanguinity was present in 40%. Patients were diagnosed as follows: FMF, 50%; CRMO, 23.5%; CINCA, 8.8%; EOS, 8.8%; MWS, 6%; and PFAPA, 2.9%. The referral diagnosis was inaccurate in all patients except for FMF patients. Gene study was informative in 9 of 14 FMF patients who had molecular analyses. None of our cohort had amyloidosis. All CRMO patients had a favorable response to treatment except 1 patient, who had refractory, progressive disease. All patients with EOS had multiorgan involvement, including uveitis. All CINCA patients had a favorable response to anakinra.
Our report shows that autoinflammatory diseases other than FMF may be overlooked. Increased awareness among pediatricians about these conditions will help to provide better health care to patients in the form of early diagnosis and management.
沙特阿拉伯已发表的关于自身炎症性疾病的数据稀缺。在本研究中,我们描述了沙特儿童自身炎症性疾病的临床和实验室特征。
2010年1月至2010年6月进行的一项基于医院的回顾性研究。
纳入过去10年在利雅得法赫德国王专科医院及研究中心儿科风湿病诊所接受治疗的自身炎症性疾病患者。自身炎症性疾病包括以下几种:家族性地中海热(FMF);慢性复发性多灶性骨髓炎(CRMO);早发型结节病(EOS);周期性发热、阿弗他口炎、咽炎和颈淋巴结炎综合征(PFAPA);慢性婴儿神经皮肤和关节综合征(CINCA);以及穆克-韦尔斯综合征(MWS)。收集了人口统计学特征、诊断、发病年龄、病程、随访时间、临床和实验室变量以及结局数据。收集的实验室数据是患者常规医疗护理的一部分。
纳入了34例自身炎症性疾病患者(女性占53%)(平均年龄151个月)。平均病程为118个月;平均发病年龄为32个月;40%的患者有近亲结婚史。患者的诊断如下:FMF占50%;CRMO占23.5%;CINCA占8.8%;EOS占8.8%;MWS占6%;PFAPA占2.9%。除FMF患者外,所有患者的转诊诊断均不准确。14例接受分子分析的FMF患者中有9例基因研究结果明确。我们的队列中无一例发生淀粉样变性。除1例患有难治性、进行性疾病的患者外,所有CRMO患者对治疗反应良好。所有EOS患者均有多器官受累,包括葡萄膜炎。所有CINCA患者对阿那白滞素反应良好。
我们的报告表明,除FMF外的自身炎症性疾病可能被忽视。儿科医生对这些疾病的认识提高将有助于以早期诊断和管理的形式为患者提供更好的医疗服务。