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
  • [31] Clinical phenotypes of adult-onset Behçet's syndrome: a comprehensive cross-sectional study in China
    She, Chun-Hui
    Hu, Dan
    Zou, Jun
    Bao, Hua-Fang
    Shen, Yan
    Cai, Jian-Fei
    Ye, Jing-Fen
    Luo, Dan
    Jian, Lei-Lei
    Ma, Hai-Fen
    Hou, Cheng-Cheng
    Chen, Yong
    Guan, Jian-Long
    CLINICAL RHEUMATOLOGY, 2024, 43 (07) : 2261 - 2271
  • [32] Rhesus monkeys as a translational model for late-onset Alzheimer's disease
    Souder, Dylan C.
    Dreischmeier, Isabelle A.
    Smith, Alex B.
    Wright, Samantha
    Martin, Stephen A.
    Sagar, Md Abdul Kader
    Eliceiri, Kevin W.
    Salamat, Shahriar M.
    Bendlin, Barbara B.
    Colman, Ricki J.
    Beasley, T. Mark
    Anderson, Rozalyn M.
    AGING CELL, 2021, 20 (06)
  • [33] Hemophagocytic Syndrome in a Patient with Adult-onset Still's Disease
    Calik, Yalkin
    Ataoglu, Safinaz
    Bas, Ersun
    Yazici, Selma
    Baki, Ali Erdem
    Yavuz, Metin
    TURKISH JOURNAL OF RHEUMATOLOGY, 2011, 26 (02) : 150 - 153
  • [34] Characteristics of Behcet's Disease in the American Southwest
    Muruganandam, Maheswari
    Rolle, Noelle A.
    Sibbitt, Wilmer L., Jr.
    Cook, Gladys B.
    Emil, N. Suzanne
    Fangtham, Monthida
    Reiter, Kimberly J.
    Bankhurst, Arthur D.
    SEMINARS IN ARTHRITIS AND RHEUMATISM, 2019, 49 (02) : 296 - 302
  • [35] Late-onset Adamantiades-Behcet's disease-systematic review and meta-analysis
    Vaiopoulos, A. G.
    Samarkos, M.
    Kanakis, M. A.
    Vaiopoulos, G.
    Kaklamanis, P. G.
    Zouboulis, C. C.
    JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY, 2024, 38 (03) : e238 - e241
  • [36] Late-onset Huntington's disease: Diagnostic and prognostic considerations
    Koutsis, Georgios
    Karadima, Georgia
    Kladi, Athina
    Panas, Marios
    PARKINSONISM & RELATED DISORDERS, 2014, 20 (07) : 726 - 730
  • [37] Clinical profiles of late-onset semantic dementia, compared with early-onset semantic dementia and late-onset Alzheimer's disease
    Shimizu, Hideaki
    Komori, Kenjiro
    Fukuhara, Ryuji
    Shinagawa, Shunichiro
    Toyota, Yasutaka
    Kashibayashi, Tetsuo
    Sonobe, Naomi
    Matsumoto, Teruhisa
    Mori, Takaaki
    Ishikawa, Tomohisa
    Hokoishi, Kazuhiko
    Tanimukai, Satoshi
    Ueno, Shu-ichi
    Ikeda, Manabu
    PSYCHOGERIATRICS, 2011, 11 (01) : 46 - 53
  • [38] Beh‡et's disease
    Koetter, I.
    Xenitidis, T.
    Fierlbeck, G.
    Schanz, S.
    Melms, A.
    Horger, M.
    Ernemann, U.
    Deuter, C.
    ZEITSCHRIFT FUR RHEUMATOLOGIE, 2012, 71 (08): : 685 - 696
  • [39] Clinical and genetic characteristics of late-onset Huntington's disease in a large European cohort
    Petracca, Martina
    Di Tella, Sonia
    Solito, Marcella
    Zinzi, Paola
    Lo Monaco, Maria Rita
    Di Lazzaro, Giulia
    Calabresi, Paolo
    Silveri, Maria Caterina
    Bentivoglio, Anna Rita
    EUROPEAN JOURNAL OF NEUROLOGY, 2022, 29 (07) : 1940 - 1951
  • [40] Characteristics and phenotype heterogeneity in late-onset Behcet's syndrome: a cohort from a referral center in China
    Zou, Jun
    Luo, Dan
    Shen, Yan
    Guan, Jian-long
    CLINICAL RHEUMATOLOGY, 2021, 40 (06) : 2319 - 2326