Purpose: We report our clinical experience with Behcet's syndrome and bladd
er involvement.
Materials and Methods: From April 1991 through July 1996, 7 men and 1 woman
25 to 53 years old with Behcet's syndrome were evaluated for lower urinary
tract symptoms (7) or hematuria (1). Of 8 patients 5 had neurological invo
lvement. Evaluation consisted of history, physical examination, urinalysis
and urine culture, excretory urography, urodynamic studies, urethrocystosco
py, bladder biopsies and histopathological examination.
Results: Cystoscopy revealed bladder ulcer in 1 patient and an indurated, h
ypervascular lesion in another with bilateral hydronephrosis. The most comm
on urodynamic finding was detrusor overactivity. Of 4 patients with poor co
mpliance 1 had additional sphincteric deficiency. Common histopathological
features were moderate and marked thickening of bladder vessel walls. Lymph
ocytic vascular reaction was present in 2 patients and lymphocytic vasculit
is in 1. Clamshell augmentation ileocystoplasty was performed in 3 patients
, including 1 who also underwent a sphincter enhancement procedure. The rem
aining 5 patients received various nonsurgical treatment.
Conclusions: Various types of voiding dysfunction relating to bladder and s
phincteric components in both phases of micturition can be seen in Behcet's
syndrome. Voiding dysfunction can be due to either neurological or direct
bladder involvement. Augmentation ileocystoplasty is a good treatment optio
n for Behcet's syndrome with severe bladder involvement.