Résumé
Behcet's disease is a chronic multisystem inflammatory disorder. Genetic, environmental, and immunological factors have been suggested as possible causes of Behcet's disease. Although seen at any age, Behcet's disease generally begins when individuals are in their 20s or 30s. The common major symptoms of Behcet's disease include recurrent oral ulcers, genital ulcers, and eye inflammation. The disorder may also cause various skin lesions, arthritis, bowel inflammation, meningitis, and cranial nerve palsies. The common urinary system manifestations are glomerulonephritis, cystitis, epididymitis, orchitis, and genital ulceration, whereas ureteral ulcers and strictures are uncommon. Here, we report an uncommon case of a ureteral ulcer and stricture in a 34-year-old man with Behcet's disease.
Sujets)
Adulte , Humains , Mâle , Arthrite , Sténose pathologique , Atteintes des nerfs crâniens , Cystite , Épididymite , Oeil , Glomérulonéphrite , Facteurs immunologiques , Inflammation , Méningite , Ulcère buccal , Orchite , Peau , Ulcère , UretèreRésumé
Congenital renal arteriovenous fistula is a rare disease and manifested by gross hematuria, bladder tamponade and flank pain. We experienced one case of congenital renal arteriovenous firstula which was cirsoid type and treated with superselective transcatheter arterial embolization of four small segmental arteries. The microcoils made of platinum and synthetic fiber were used as theembolization modality.
Sujets)
Artères , Fistule artérioveineuse , Douleur du flanc , Hématurie , Platine , Maladies rares , Vessie urinaireRésumé
Urethral caruncles are the most common benign tumors in the female urethra, and are usually found in the posterior lip of the urethral meatus of post-menopausal women. It is very rare in young girls. Its etiology is unknown. We add a case of urethral caruncle occurring in a 2 year and 5 month-old girl's mid-urethra. We believe that further accumulation of unusual cases may be helpful in discovering the pathogenesis.