Kassir Radwan, Mouracade Pascal, Barabino Gabriele, Peoc'h Michel, Cuilleron Muriel, Gigante Marc
Department of General Surgery, CHU Hospital, Jean Monnet University, Saint Etienne, France.
Int J Surg Case Rep. 2013;4(9):782-4. doi: 10.1016/j.ijscr.2013.06.001. Epub 2013 Jun 14.
Isolated vasculitis of the bladder is extremely rare. The main causes of which are auto-immune diseases and occasionally infections. Corticosteroid therapy plays a central role in treatment in the majority of cases.
We report a case of gross hematuria associated with irritative low urinary tract symptoms (LUTS) and an increase of biological parameters of inflammation. Radiologic studies suspected a pelvic tumor process. We performed a cystoscopy with multiple biopsies. The pathological findings of the chips were in favor of a thrombotic nongranulomatous vasculitis of small and medium caliber. In view of these findings, all systemic diseases and inflammatory diseases such as cryoglobulinemia, the anti-phospholipid syndrome, Crohn's disease were eliminated. The symptoms regressed completely under antibiotics and anticoagulants.
Our treatment options were based on the extent of the acute phase reaction and the pelvic venous thrombosis. A few similar cases have been reported in the literature, particularly a case of isolated necrotizing vasculitis of the bladder involving small vessels with a mild laboratory acute phase reaction which was treated with corticosteroids and cyclophosphamide.
It is important to differentiate this rare pathological feature of the bladder from other bladder tumors as the treatment is medical rather than surgical.