A national cohort study on pediatric Behcet's disease: cross-sectional data from an Italian registry

被引:57
作者
Gallizzi, Romina [1 ]
Pidone, Caterina [1 ]
Cantarini, Luca [2 ]
Finetti, Martina [3 ]
Cattalini, Marco [4 ,5 ]
Filocamo, Giovanni [6 ]
Insalaco, Antonella [7 ]
Rigante, Donato [8 ]
Consolini, Rita [9 ]
Maggio, Maria Cristina [10 ]
Civino, Adele [11 ]
Martino, Silvana [12 ]
Olivieri, Alma Nunzia [13 ]
Fabio, Giovanna [14 ]
Pastore, Serena [15 ]
Mauro, Angela [18 ]
Sutera, Diana [1 ]
Trimarchi, Giuseppe [16 ]
Ruperto, Nicolino [17 ]
Gattorno, Marco [17 ]
Cimaz, Rolando [18 ]
机构
[1] Univ Messina, Dept Human Pathol Adulthood & Childhood G Barresi, Unit Pediat, Messina, Italy
[2] Univ Siena, Rheumatol Unit, Policlin Le Scotte, Siena, Italy
[3] Gaslini Inst, Unit Pediat 2, Genoa, Italy
[4] Univ Brescia, Pediat Clin, Brescia, Italy
[5] Spedali Civili Brescia, Brescia, Italy
[6] Fdn IRCCS Ca Grande, Osped Maggiore, Pediat Rheumatol, Milan, Italy
[7] Bambino Gesu Pediat Hosp, Div Rheumatol, Dept Pediat Med, Rome, Italy
[8] Univ Cattolica Sacro Cuore, Inst Pediat, Fdn Policlin Univ, Rome, Italy
[9] AOU, Unit Pediat, Pisa, Italy
[10] Osped Bambini G Di Cristina, Palermo, Italy
[11] Azienda Osped Card G Panico, Lecce, Italy
[12] Osped Regina Margherita, Unit Pediat, Turin, Italy
[13] Second Univ Study Napoli, Naples, Italy
[14] Fdn IRCCS Ca Grande Osped Maggiore, Milan, Italy
[15] IRCCS Burlo Garofalo, Trieste, Italy
[16] Univ Messina, Dipartimento Econ Messina, Messina, Italy
[17] Inst G Gaslini, UO Pediat 2, Genoa, Italy
[18] Univ Florence, Pediat Rheumatol Unit, AOU Meyer, Florence, Italy
来源
PEDIATRIC RHEUMATOLOGY | 2017年 / 15卷
关键词
Behcet's disease; Children; Clinical features; Diagnostic criteria; Treatment; CHILDREN; MULTICENTER; CRITERIA; UPDATE;
D O I
10.1186/s12969-017-0213-x
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background: Behcet's disease is a rare multi-systemic inflammatory disease with unknown etiology which involves principally oral and genital mucosa, skin and eyes. Average age at onset of the disease is about 25-30 years, but it may be diagnosed before the age of 16. It is not very rare in Italy, even though there are limited data concerning epidemiology. Aim of this study is to describe the baseline data of an Italian cohort of patients with as having BD or probable BD. Methods: We described the baseline data of the first national epidemiological study on children coming from 16 Italian Pediatric Rheumatologic Centers diagnosed by the treating physicians as having Behcet's Disease. Data on demographic characteristics, clinical features and therapy were collected. We then compared our findings to those of international pediatric cohort studies and also retrospectively evaluated the ability to diagnose BD using ISG, ICBD and, for the first time, the new PEDBD criteria. Results: The study included 110 patients (62 M, 48F). Average age at onset was 8.34 +/- 4.11 years. The frequencies of signs/symptoms were: recurrent oral aphtosis 94.5%, genital ulcers 33.6%, ocular 43.6%, gastrointestinal 42.7%, musculoskeletal 42.7%, neurological 30.9% and vascular involvement 10%. Thirty-two patients (29.1%) fulfilled ISG, 78 (70.9%) ICBD, 50 (45.5%) PEDBD criteria and 31 (28%) didn't fulfill any of them. The most frequently used treatments were colchicine and corticosteroids followed by immunosuppressants. Four patients received biologic therapy (anti TNF-alpha and anti-IL-1) to treat severe organ involvement. Conclusions: Recurrent oral aphtosis was the most frequent clinical manifestation, followed by ocular involvement. Gastrointestinal lesions were more frequent in Italy than in non-European countries as opposed to genital ulcers. Skin, ocular and vascular manifestations had a higher frequency in males and genital ulcers in females. Constitutional symptoms were present in 44.5% and recurrent fever in one third of our population.
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