Literature DB >> 17076707

Clinical features of late-onset Behçet's disease: report of nine cases.

Hayriye Saricaoglu1, Serap Koran Karadogan, Neval Bayazit, Ali Yucel, Kamil Dilek, Sukran Tunali.   

Abstract

BACKGROUND: Behçet's disease (BD) is usually diagnosed between the second and fourth decades. Onset after 50 years of age is extremely rare. We aimed to analyze the clinical features of late-onset patients with BD.
METHOD: The study was conducted from 439 patients diagnosed as BD according to criteria of the International Study Group for BD. Clinical features of patients who were asymptomatic or suffered from only recurrent aphthous stomatitis (RAS) until 50 years of age but fulfilled the diagnostic criteria of BD after this age were reviewed.
RESULTS: The age-of-onset was more than 50 years in nine patients (1.56%). Two patients developed erythema nodosum, two developed pathergy positivity, one developed papulopustules, pathergy positivity and ocular symptoms, one developed papulopustules and pathergy positivity, one developed ocular symptoms, one developed papulopustules and ocular symptoms, and one developed erythema nodosum and pathergy positivity as well as oral aphthae and genital ulcerations after the age of 50 years. The neurologic system was involved in two patients. Mucocutaneous symptoms of two patients worsened after interruption of therapy. Two patients with neurologic and ocular involvement flared during the follow up.
CONCLUSION: Since the course of the disease is regarded to be relatively mild in mature patients, it is noteworthy that systemic manifestations such as ocular and neurologic involvement and acute flares developed after the age of 50 years in the limited number of patients with late-onset BD in our series.

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Year:  2006        PMID: 17076707     DOI: 10.1111/j.1365-4632.2006.02921.x

Source DB:  PubMed          Journal:  Int J Dermatol        ISSN: 0011-9059            Impact factor:   2.736


  4 in total

1.  Late-onset Behçet's disease: demographic, clinical, and ocular features.

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2.  Behçet's Uveitis.

Authors:  Ilknur Tugal-Tutkun
Journal:  Middle East Afr J Ophthalmol       Date:  2009-10

Review 3.  Gender and ocular manifestations of connective tissue diseases and systemic vasculitides.

Authors:  Maria M Choudhary; Rula A Hajj-Ali; Careen Y Lowder
Journal:  J Ophthalmol       Date:  2014-03-17       Impact factor: 1.909

4.  Clinical phenotypes of Korean patients with Behcet disease according to gender, age at onset, and HLA-B51.

Authors:  Hee Jung Ryu; Mi Ryoung Seo; Hyo Jin Choi; Han Joo Baek
Journal:  Korean J Intern Med       Date:  2017-01-12       Impact factor: 2.884

  4 in total

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