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1.
J Eur Acad Dermatol Venereol ; 24(4): 434-8, 2010 Apr.
Article in English | MEDLINE | ID: mdl-19758264

ABSTRACT

BACKGROUND: This is the largest specific demographic and clinical study performed until now in Greece. OBJECTIVES: To analyse the spectrum of mucocutaneous manifestations in 202 patients with Adamantiades-Behçet's disease (ABD) in Greece. METHODS: Any mucocutaneous symptom at disease onset and during the follow-up was recorded in a particular questionnaire that included 58 items. All patients fulfilled the International Study Group Criteria for BD. RESULTS: Consecutive patients (130 men and 72 women) were included in this study. Their mean age was 42.03 +/- 12.41 and 44.96 +/- 11.99 years for male and female patients respectively. Pathergy test was positive in 38%, whereas HLA-B5 (51) positivity was evident in 76% of patients. Onset signs: oral aphthous ulcers were found in 64.36%, genital ulcers in 6.93%, skin lesions in 8.91%, erythema nodosum in 7.42% and pseudofolliculitis in 1.5%. One patient had leg ulcers. During the follow-up, oral aphthous ulcers were found in 100%, genital ulcers in 65.4% and in 51.4%, erythema nodosum in 42.9% and in 78.1%, whereas pseudofolliculitis in 57.1% and in 21.9% in men and women respectively. Significant differences pointing to a different course of mucocutaneous disease were found between men and women. CONCLUSIONS: The nature and frequency of mucocutaneous manifestations at presentation are important for the diagnosis of ABD, whereas significant differences were found between genders in this Greek patient cohort. Significant differences were also observed when our results were compared with those of four other series, probably explained by genetic and environmental factors.


Subject(s)
Behcet Syndrome/epidemiology , Behcet Syndrome/pathology , Oral Ulcer/epidemiology , Oral Ulcer/pathology , Skin Diseases/epidemiology , Skin Diseases/pathology , Adult , Age of Onset , Female , Follow-Up Studies , Genital Diseases, Female/epidemiology , Genital Diseases, Female/pathology , Genital Diseases, Male/epidemiology , Genital Diseases, Male/pathology , Greece/epidemiology , Humans , Male , Middle Aged , Mucous Membrane/pathology , Risk Factors , Severity of Illness Index , Sex Characteristics
2.
Clin Exp Rheumatol ; 25(4 Suppl 45): S65-9, 2007.
Article in English | MEDLINE | ID: mdl-17949554

ABSTRACT

OBJECTIVE: To study autoantibody formation in patients with Behçet's disease (BD) who received long-term treatment with the anti-TNF monoclonal antibody infliximab. METHODS: Serial sera from infliximab-treated patients (5 mg/kg at weeks 0, 4, 8, and every 6-8 weeks thereafter) were tested for various autoantibodies, using commercially available methods, at baseline and at 6 months (n = 20), at 12 months (n = 16), and at 18 months post-baseline (n = 12). Thirty-five age- and sex-matched BD patients, not treated with infliximab, served as controls. RESULTS: Autoantibodies were rarely seen in controls, as well as in infliximab treated patients at baseline. Formation of antinuclear antibodies (ANA) at low titers was evident in 13/20 (65%) patients at 6 months post-baseline; one additional patient developed anti-beta2 glycoprotein-I IgM antibodies (anti-beta(2)GPI). Of the 13 ANA-positive sera, low titers-IgM of anti-dsDNA or anti-beta(2)GPI were detected in 7 (35%) and 6 (30%) patients, respectively. Additional measurements at 12 and 18 months showed that the persistence and/or increasing titers of these autoantibodies depended on continuation of treatment. Antibodies to extractable nuclear antigens (anti-RNP, anti-SS-A/Ro, anti-SS-B/La, anti-Sm), rheumatoid factors, anti-cyclic citrullinated peptide antibodies and antineutrophil cytoplasmic antibodies, were never detected. No antibody-related symptoms, lupus-like disease, or thrombosis were observed in any patient up to 18 months of follow-up. CONCLUSION: Early induction of ANA and specific autoantibodies is common in BD patients treated with infliximab, including low titers of non-pathogenic anti-dsDNA and anti-Beta2GPI antibodies. A possible clinical significance of these findings needs to be documented in further studies, including more patients and longer follow-up periods.


Subject(s)
Antibodies, Monoclonal/adverse effects , Autoantibodies/immunology , Behcet Syndrome/drug therapy , Immunologic Factors/adverse effects , Tumor Necrosis Factor-alpha/antagonists & inhibitors , Adult , Autoantibodies/metabolism , Case-Control Studies , Female , Humans , Infliximab , Male , Middle Aged , Prospective Studies
4.
Clin Exp Rheumatol ; 13(5): 649-51, 1995.
Article in English | MEDLINE | ID: mdl-8575147

ABSTRACT

Pericardial involvement in Adamantiadis-Behçet's disease (ABD) is uncommon. A 14-year-old boy presented with fever of unknown origin, as the initial and only manifestation of his disease. Other features were leukopenia, abdominal lymphadenopathy and asymptomatic pericarditis, which is a very rare finding of the disease. A review of pericarditis is presented.


Subject(s)
Behcet Syndrome/complications , Pericarditis/etiology , Adolescent , Behcet Syndrome/diagnosis , Humans , Male , Pericarditis/diagnosis
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