A 59-year-old male patient who had no previous history of tuberculosis visited our clinic for abrupt onset gross hematuria in 2008. Cystoscopy performed at that time showed a diffuse papillary mass on the posterior wall. Accordingly, TURB was performed, and the mass was completely removed without any remnant mass. Based on pathology results, the patient was diagnosed with high grade transitional cell carcinoma (T1) of bladder, and accordingly, intravesical BCG (OncoTice, Organon Teknika, Boxtel, The Netherland) instillation were performed once a week for 6 weeks at a concentration of 12.5 mg in 60-mL saline. Thereafter, the patient underwent cystoscopy regularly in outpatient clinics, and underwent three booster BCG intravesical therapy sessions in 2009, but showed no signs of recurrent cancer. Although no voiding symptoms were observed, PSA levels that were coincidentally measured were high. When the patient visited our clinic in 2015, a PSA level of 3.08 ng/mL was found, higher than that measured in 2008 of 0.76 ng/m, and was later elevated to 4.07 ng/mL. However, the patient had no voiding symptoms or subjective symptoms such as perineal discomfort, and no abnormal findings were made in transrectal prostate ultrasonography with regard to prostate volume, which was 27 g, and abscess pocket (
Fig. 1). Because the patient's PSA level continued to elevate, the patient was suspected to have prostate cancer, and accordingly, an ultrasonography-guided 12-core prostate biopsy was performed in 2016. The patient was diagnosed with chronic granulomatous prostatitis with caseation necrosis based on pathology results (
Figs. 2,
3). The patient has been on antituberculosis medications since a Ziehl-Neelsen stain revealed a positive acid-fast bacilli. He is scheduled for a follow-up prostate biopsy at the end of the 6-month pharmacotherapy of isoniazid (300 mg), rifampicin (600 mg), etambutol (800 mg), and pyrazinamide (1,500 mg) daily. And the PSA level fell to 1.48 ng/mL at the same time.