Characteristics of late-onset Behçet's disease and comparison with juvenile and adult-onset Behcet's disease

被引:0
|
作者
Boluk, Kuebra Nursel [1 ]
Kose, Afet Akdag [1 ]
机构
[1] Istanbul Univ, Istanbul Fac Med, Dept Dermatol & Venereol, Millet St Caddesi, TR-34093 Istanbul, Turkiye
关键词
Behcet's disease; late-onset Behcet's disease; adult-onset Behcet's disease; juvenile Behcet's disease; CLINICAL-FEATURES; VASCULAR INVOLVEMENT; PATHERGY REACTION; MANIFESTATIONS; PREVALENCE; SEX; AGE; NATIONWIDE; MORTALITY; HLA-B51;
D O I
10.1111/ijd.17456
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background The course of late-onset Beh & ccedil;et's disease (LBD) is unknown. This study aimed to determine the characteristics and systemic involvement of LBD. Methods In this retrospective, cross-sectional, and comparative study, 700 patient files from 4100 patients diagnosed with Behcet's disease (BD) were selected and divided into three groups: LBD, adult BD (ABD), and juvenile BD (JBD). The age limits for LBD and JBD were determined to be 42 and 16, respectively. LBD patients were compared to ABD and JBD patients in terms of demographics, systemic involvement, and disease duration. Results The LBD rate among BD patients was 4.7% (183/4,100). The time from initial symptom occurrence to the age at which the BD criteria were met was longer in LBD than in ABD or JBD. Except for genital ulcers, the frequencies of involvement in LBD were similar to those in ABD and JBD. The frequency of family history was significantly lower in LBD (12%) than in ABD (15.9%) or JBD (18.2%). The time from the initial symptom to oral aphthae, genital ulcers, and eye involvement was longer in LBD than in ABD or JBD. Furthermore, erythema nodosum was observed after a longer duration in LBD than in ABD. Conclusion Considering that involvement occurs much later in LBD and there are no differences in the frequencies of involvement except for genital ulcers, LBD patients should be followed up as closely as ABD and JBD patients.
引用
收藏
页码:e383 / e389
页数:7
相关论文
共 50 条
  • [1] Late-onset Beh‡et's disease: demographic, clinical, and ocular features
    Sungur, Gulten
    Hazirolan, Dicle
    Hekimoglu, Emre
    Kasim, Remzi
    Duman, Sunay
    GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, 2010, 248 (09) : 1325 - 1330
  • [2] Late onset Behcet's disease
    Ziade, Nelly
    Awada, Hassane
    JOINT BONE SPINE, 2006, 73 (05) : 567 - 569
  • [3] Childhood Behcet's disease: clinical features and comparison with adult-onset disease
    Krause, I
    Uziel, Y
    Guedj, D
    Mukamel, M
    Harel, L
    Molad, Y
    Weinberger, A
    RHEUMATOLOGY, 1999, 38 (05) : 457 - 462
  • [4] Adult-onset Still's disease
    Bagnari, Valentina
    Colina, Matteo
    Ciancio, Giovanni
    Govoni, Marcello
    Trotta, Francesco
    RHEUMATOLOGY INTERNATIONAL, 2010, 30 (07) : CP9 - 862
  • [5] Adult-onset Still's disease
    Gerfaud-Valentin, Mathieu
    Jamilloux, Yvan
    Iwaz, Jean
    Seve, Pascal
    AUTOIMMUNITY REVIEWS, 2014, 13 (07) : 708 - 722
  • [6] Clinical characteristics and treatment of elderly onset adult-onset Still's disease
    Kishida, Dai
    Ichikawa, Takanori
    Takamatsu, Ryota
    Nomura, Shun
    Matsuda, Masayuki
    Ishii, Wataru
    Nagai, Tatsuo
    Suzuki, Sadahiro
    Ueno, Ken-ichi
    Tachibana, Naoki
    Shimojima, Yasuhiro
    Sekijima, Yoshiki
    SCIENTIFIC REPORTS, 2022, 12 (01)
  • [7] Ocular Manifestations of Late-Onset Behcet Disease
    Citirik, Mehmet
    Berker, Nilufer
    Songur, Murat Serkan
    Ozkan, Seyhan Sonar
    Zilelioglu, Orhan
    OPHTHALMOLOGICA, 2011, 225 (01) : 21 - 26
  • [8] Clinical and genetic characteristics of late-onset Huntington's disease
    Oosterloo, Mayke
    Bijlsma, Emilia
    van Kuijk, Sander
    Minkes, Floor
    Roos, Raymund
    de Die-Smulders, C. E. M.
    PARKINSONISM & RELATED DISORDERS, 2019, 61 : 101 - 105
  • [9] Clinical characteristics and outcome of elderly onset adult-onset Still?s disease: A 10-year retrospective study
    Li, Sheng
    Ying, Shuni
    Bai, Juan
    Wang, Yuqian
    Yang, Changyi
    Sun, Qingmiao
    Fang, Hong
    Qiao, Jianjun
    JOURNAL OF TRANSLATIONAL AUTOIMMUNITY, 2023, 6
  • [10] Cardiac Tumor in Juvenile Onset Behçet’s Disease: Case Report and Review of the Literature
    Elizabeth E. Adams
    Vincent P. R. Aluquin
    C. April Bingham
    James R. Stone
    Linda B. Pauliks
    Pediatric Cardiology, 2010, 31 : 277 - 279