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EULAR/PRINTO/PRES criteria for Henoch-Schonlein purpura, childhood polyarteritis nodosa, childhood Wegener granulomatosis and childhood Takayasu arteritis: Ankara 2008. Part II: Final classification criteria

医学 过敏性紫癜 结节性多动脉炎 血管炎 动脉炎 紫癜(腹足类) 系统性血管炎 病理 内科学 胃肠病学 疾病 生态学 生物
作者
Seza Özen,Angela Pistorio,Silvia M. Iusan,Ayşı̇n Bakkaloğlu,T Herlin,Riva Brik,Antonella Buoncompagni,Călin Lazăr,İlmay Bilge,Yosef Uziel,Donato Rigante,Luca Cantarini,Maria Odete Esteves Hilário,C. A. Silva,Margarita Alegrı́a,Ximena Norambuena,Alexandre Belot,Yackov Berkun,A. I. Estrella,Alma Nunzia Olivieri,M. G. Alpigiani,I. Rumba,Flávio Sztajnbok,Lana Tambić-Bukovac,Luciana Breda,Sulaiman M. Al‐Mayouf,Dimitrina Mihaylova,В. Г. Часнык,Claudia Sengler,Marisa Klein-Gitelman,D. Djeddi,Laura Nuño,Chris Pruunsild,Juergen Brunner,Anuela Kondi,K I Pagava,Silvia Pederzoli,Alberto Martini,Nicolino Ruperto
出处
期刊:Annals of the Rheumatic Diseases [BMJ]
卷期号:69 (5): 798-806 被引量:1036
标识
DOI:10.1136/ard.2009.116657
摘要

Objectives

To validate the previously proposed classification criteria for Henoch–Schönlein purpura (HSP), childhood polyarteritis nodosa (c-PAN), c-Wegener granulomatosis (c-WG) and c-Takayasu arteritis (c-TA).

Methods

Step 1: retrospective/prospective web-data collection for children with HSP, c-PAN, c-WG and c-TA with age at diagnosis ≤18 years. Step 2: blinded classification by consensus panel of a representative sample of 280 cases. Step 3: statistical (sensitivity, specificity, area under the curve and κ-agreement) and nominal group technique consensus evaluations.

Results

827 patients with HSP, 150 with c-PAN, 60 with c-WG, 87 with c-TA and 52 with c-other were compared with each other. A patient was classified as HSP in the presence of purpura or petechiae (mandatory) with lower limb predominance plus one of four criteria: (1) abdominal pain; (2) histopathology (IgA); (3) arthritis or arthralgia; (4) renal involvement. Classification of c-PAN required a systemic inflammatory disease with evidence of necrotising vasculitis OR angiographic abnormalities of medium-/small-sized arteries (mandatory criterion) plus one of five criteria: (1) skin involvement; (2) myalgia/muscle tenderness; (3) hypertension; (4) peripheral neuropathy; (5) renal involvement. Classification of c-WG required three of six criteria: (1) histopathological evidence of granulomatous inflammation; (2) upper airway involvement; (3) laryngo-tracheo-bronchial involvement; (4) pulmonary involvement (x-ray/CT); (5) antineutrophilic cytoplasmic antibody positivity; (6) renal involvement. Classification of c-TA required typical angiographic abnormalities of the aorta or its main branches and pulmonary arteries (mandatory criterion) plus one of five criteria: (1) pulse deficit or claudication; (2) blood pressure discrepancy in any limb; (3) bruits; (4) hypertension; (5) elevated acute phase reactant.

Conclusion

European League Against Rheumatism/Paediatric Rheumatology International Trials Organisation/Paediatric Rheumatology European Society propose validated classification criteria for HSP, c-PAN, c-WG and c-TA with high sensitivity/specificity.
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