Research Article

High Incidence of Gastrointestinal Ulceration and Cytogenetic Aberration of Trisomy 8 as Typical Features of Behçet’s Disease Associated with Myelodysplastic Syndrome: A Series of 16 Consecutive Chinese Patients from the Shanghai Behçet’s Disease Database and Comparison with the Literature

Table 1

Clinical characteristics of patients with BD and/without MDS.

BD with MDS 
()
BD without MDS 
()

Age at BD diagnosis (y), mean (SD)49.9 ± 12.437.9 ± 12.80.00
Age at MDS diagnosis (y), mean (SD)47.5 ± 12.2--
Male (%)4 (25.0)409 (51.8)0.04
Oral ulcer16 (100)777 (98.5)0.821
Genital ulcer14 (87.5)558 (70.7)0.432
Ocular lesion0 (0)102 (12.9)0.391
Arthritis5 (31.3)178 (22.6)0.714
Skin lesions7 (43.8)510 (64.6)0.084
Positive pathergy test3 (18.8)55 /125 (44.0)0.062
Central nervous system0 (0)14 (1.8)>0.99
Vascular lesions0 (0)31 (3.9)>0.99
GI involvement10 (62.5)94 (11.9)<0.00
Fever9 (56.3)7 (1.9)<0.00
Laboratory findings at diagnosis of BD
 CRP (mg/L)54.8 ± 40.812.74 ± 22.160.00
 ESR (mm/h)80.2 ± 29.723.74 ± 24.38<0.00
 WBC (109/L)3.6 ± 2.27.2 ± 2.5<0.00
 Hemoglobin (g/L)88.8 ± 18.7135.6 ± 19.4<0.00
 Platelets (109/L)144.0 ± 109.0228.5 ± 75.90.01

. BD: Behçet disease; GI: gastrointestinal; CRP: C-reactive protein; ESR: erythrocyte sedimentation rate; WBC: white blood cells.