Treatment of Prostatic Abscess: Value of Transrectal Ultrasonographically Guided Needle Aspiration Joo Won Lim, MD, Young Tae Ko, MD, Dong Ho Lee, MD, Seong Jin Park, MD, Joo Hyeong Oh, MD, Yup Yoon, MD, Sung-Goo Chang, MD The purpose of this study was to assess the effectiveness of transrectal ultrasonographically guided needle aspiration in the treatment of prostatic abscess. Fourteen patients with prostatic abscess were evaluated with this technique and treated with sonographically guided needle aspiration. Using this technique, all cases (100%) had one or more hypoechoic areas within the prostate that contained inhomogeneous materials; in 10 patients (71.0%), the lesion showed internal septa or solid portion. The margins of the hypoechoic area were well defined and thick in 11 patients (79.0%) and poorly defined in 3 patients (21.0%). The estimated volume of the prostatic abscess ranged between 2 and 28 ml (mean, 12.0 ml). The presence of a pus collection within the prostate was confirmed by transrectal ultrasonographically guided aspiration in all patients. However, successful treatment of prostatic abscess with transrectal needle aspiration was done in 12 (86.0%) of 14 patients; the treatment failed in 2 (14.0%) of 14 patients. One patient was treated with perineal incision and drainage and the other with transurethral resection. The amount of pus drained ranged between 1 and 39 ml (mean, 12.0 ml). On follow-up transrectal ultrasonographic examination, no remaining abscess pocket was found within the prostate in any of the cases. One year later, the prostatic abscess recurred in one case. In conclusion, transrectal ultrasonographic guidance is useful in the diagnosis of prostatic abscess as well as in the guidance for aspiration and the drainage of such abscesses. Transrectal ultrasonographically guided needle aspiration could be an effective method for treating prostatic abscess. KEY WORDS: Prostate, abscess; Abscess, prostatic; Abscess, percutaneous drainage. P ABBREVIATIONS TRUS, Transrectal ultrasonography; PA, Prostatic abscess; CT, Computed tomography; MR, Magnetic resonance; ICT, Intracavitary transducer Received January 3, 2000, from the Departments of Diagnostic Radiology (J.W.L., Y.T.K., D.H.L., S.J.P., J.H.O., Y.Y.) and Urology (S.G.C.), Kyung Hee Medical Center, Kyung Hee University, School of Medicine, Seoul, Korea. Revised manuscript accepted for publication May 28, 2000. Address correspondence and reprint requests to Joo Won Lim, MD, Department of Diagnostic Radiology, Kyung Hee Medical Center, 1 Hoe Ki Dong, Dong Dae Mun Ku, Seoul, 130-702, Korea. rostatic abscess occurs infrequently. Its signs and symptoms are not only highly variable but also similar to those of acute bacterial prostatitis without abscess. Because the diagnosis of PA is often difficult to confirm by history and physical examination, prostatic imaging (TRUS, CT, and MR imaging) can be important in the diagnosis and management.1–11 Among these, TRUS is the most widely used technique in the diagnosis and management of PA. Perineal incision and drainage, transurethral unroofing and resection into the abscess cavity, and percutaneous transperineal drainage have been used to treat PA.1–7 Although surgical drainage is the most important step in the treatment of PA, the best method of drainage remains somewhat controversial.4,5 Many investigators have used percutaneous 2000 by the American Institute of Ultrasound in Medicine • J Ultrasound Med 19:609–617, 2000 • 0278-4297/00/$3.50 610 TREATMENT OF PROSTATIC ABSCESS drainage as a treating method of intraabdominal abscess. The safety and efficacy of these methods are well established.3,5,6,12–16 However, few studies in the literature have indicated that needle aspiration and adjuvant antibiotic therapy could produce a cure.2,17,18 We report 14 cases of prostatic abscesses that were diagnosed by TRUS and treated successfully (12 of the 14 cases) with TRUS-guided needle aspiration and adjuvant antibiotic therapy. MATERIALS AND METHODS Over the course of 5 years, 14 patients with PA were evaluated by TRUS and treated with TRUS-guided needle aspiration. The clinical findings, including symptoms, history, and laboratory findings, for each patient were reviewed using the patients’ medical records. The patients ranged in age from 43 to 75 years (mean, 65.0 years). Clinical presentation for each patient is summarized in Table 1. Diagnostic modalities and results of treatment with needle aspiration in patients with PA are summarized in Table 2. Predisposing factors for PA were diabetes in five patients, instrumentation in two patients, indwelling urethral catheter in one patient, and immunosuppressive therapy after renal transplantation in one patient. Digital rectal examination was performed in eight patients. TRUS was performed with an Ultramark 9-HDI or HDI 3000 system (Advanced Technology Laboratories, Bothell, WA) using a 9-5 MHz ICT probe and an SSA 250A (Toshiba, Tokyo, Japan) using a 5 MHz convex and linear transrectal probe. All patients had a cleansing enema prior to the procedure to eliminate as much fecal material as possible. We detected abnormal foci within the prostate by TRUS in all patients. The volume of pus collection was estimated by the formula: v = 0.5 × D1 × D2 × D3 (D1, the transverse; D2, the anteroposterior; D3, the cephalocaudal dimension of PA) or by use of software provided by the manufacturer with the prolate ellipse formula. Nine patients were examined with color and power Doppler sonography using 9-5 MHz ICT probes (HDI 3000). CT was performed in one patient, and one other patient was evaluated with MR imaging. TRUS-guided aspiration was performed with an 18 gauge (20 cm long) Chiba needle (Cook, Bloomington, IN) in five patients and an 18 gauge (20 cm long) Tru-Cut needle (Medical Device Technology, Gainesville, FL) in nine patients. Patients were placed in the left lateral decubitus position with a knee-chest position. A 9-5 MHz ICT probe (Advanced Technology Laboratories) or a 5 MHz J Ultrasound Med 19:609–617, 2000 convex and linear transrectal probe (Toshiba) was covered with a condom, and a biopsy guide attachment was used for needle aspiration. The needle was inserted under TRUS guidance through the rectal wall into the abscess cavity (Fig. 1A, B). Before TRUSguided needle aspiration, we started tentative antibiotic treatment with quinolone. After the needle aspiration, parenteral antibiotic therapy was initiated in all patients. Reaccumulation of pus was monitored by TRUS. Criteria for successful treatment were clinical improvement and decrease of more than one half of the estimated volume of pus collection on followup TRUS examination (Fig. 1C). Criteria for failure included continued clinical symptoms with or without persistent or recurring fluid collection. RESULTS Clinical presentations most often included dysuria and urinary frequency (10 patients, 71%). Six patients (43%) had acute urinary retention. Four patients (29%) had fever. Other clinical presentations included hematuria in three patients (21%), low back pain in two patients (14%), and perineal pain in two patients (14%) (Table 1). We tested for leukocytes in midstream urine in all patients; eight had more than 10 leukocytes per high power field, three had from 5 to 9, and three had fewer than 4. Urine culture obtained in these patients yielded a negative result in eight (57%) and a positive result in six (43%). Pseudomonas aeruginosa was isolated in three patients, Escherichia coli in two, and Staphylococcus aureus in one (Table 2). Elevated white blood cell counts were present in seven patients. Digital rectal examination was performed in eight patients, and five cases revealed tenderness. Because the classic finding on rectal examination of a tender, fluctuant mass was absent in all cases, no case of PA was diagnosed by digital rectal examination. Table 1: Clinical Presentations in Patients with Prostatic Abscesses (n = 14) Signs or Symptoms Dysuria Urinary frequency Acute urinary retention Fever Hematuria Pain in low back Perineal pain Number of Patients Percentage (%) 10 10 6 4 3 2 2 71.0 71.0 43.0 29.0 21.0 14.0 14.0 J Ultrasound Med 19:609–617, 2000 LIM ET AL 611 Table 2: Diagnostic Modalities and Results of Treatment with Needle Aspiration in Patients with Prostatic Abscesses (n = 14) DRE Method of Diagnosis Other Diagnostic Modalities 1 Not performed TRUS CT 23 39 Success after third procedure Not identified E. coli 2 Prostate smooth and nontender TRUS None 28 20 Success after first procedure Not identified Pseudomonas aeruginosa 3 Prostate smooth and nontender TRUS None 20 18 Success after first procedure Not identified Staphylococcus aureus 4 Prostate mildly tender TRUS MRI 5 3 Success after first procedure Not identified Not identified 5 Prostate mildly tender TRUS None 5.5 3 Success after first procedure Pseudomonas aeruginosa Not identified 6 Not performed TRUS CDI 2 1 Success after first procedure Pseudomonas aeruginosa Pseudomonas aeruginosa 7 Not performed TRUS CDI 5 3.5 Failure* E. coli E. coli 8 Prostate tender TRUS CDI 10 3.5 Failure† Not identified Staphylococcus aureus 9 Not performed TRUS CDI 2 1 Success after first procedure Pseudomonas aeruginosa Not identified 10 Prostate tender TRUS CDI 19 16 Success after first procedure Staphylococcus Staphylococcus aureus aureus 11 Prostate smooth and nontender TRUS CDI 27 23 Success after second procedure Not indentified Klebsiella pneumoniae 12 Not performed TRUS CDI 7 5 Success after first procedure E. coli E. coli 13 Prostate mildly tender TRUS CDI 9 12 Success after second procedure Not identified Not identified 14 Not performed TRUS CDI 14 16 Success after second procedure Not identified Staphylococcus aureus Patient Estimated Volume Volume of of Pus (ml) Aspirate (ml) Result of Treatment with Needle Aspiration Cultured Organism Urine Aspirate DRE, Digital rectal examination; CDI, color and power Doppler imaging. *Developed periprostatic abscess after transrectal needle aspiration, which was treated with perineal incision and drainage. †Because of small aspirate volume, prostatic abscess was treated with transurethral resection. The TRUS findings in 14 patients with PA are summarized in Table 3. TRUS revealed one or more hypoechoic areas within the prostate that contained inhomogeneous material in all patients (100%); in 10 patients (71.0%), the lesion showed internal septa or solid portions. The outer margin of the hypoechoic area was well defined and thick in 11 patients (79.0%) (Fig. 1A) and poorly defined in three patients (21.0%) (Fig. 2). The prostate showed a perilesional hypoechoic area, indicating inflammatory change, in 10 patients (71.0%) (Fig. 2A). The abnormal fluid collection was extended into a periprostatic space in six patients (43.0%) (Fig. 2B). The estimated volume of the abnormal fluid collection ranged between 2 and 28 ml (mean, 12.0 ml). The number of fluid collections within the prostate was one in seven patients (50%), two in six patients (43.0%), and three in one patient (7.0%). The location of the fluid collection within the prostate was in the outer and inner glands in six patients, in the outer gland in five patients, and in the inner gland in three patients. Color and power Doppler sonography were performed in nine patients. A diffusely increased blood flow was observed at the margin of the hypoechoic area as well as in the remaining portion of the prostate in all patients (100%). No blood flow was 612 TREATMENT OF PROSTATIC ABSCESS A Figure 1 68 year old man with diabetes who had urinary frequency and dysuria. A, Transverse sonogram shows abscess as inhomogeneous hypoechoic area with well-defined margin and wall in both inner and outer parts of the gland (arrows). Estimated volume of pus is 19 ml. B, Under TRUS guidance, an 18 gauge needle (arrowheads) was inserted through the rectal wall into the abscess cavity, and 16 ml of pus was aspirated. C, Postaspiration follow-up sonogram 1 week later shows obliteration of abscess cavity (arrows). J Ultrasound Med 19:609–617, 2000 B C noted within the hypoechoic area (Fig. 3). CT was done in one patient and MR imaging was performed in another patient. Both CT and MR imaging make it possible to define the exact extents of both intraglandular and extraglandular fluid collections (Fig. 4). The presence of pus within the prostate was confirmed by TRUS-guided needle aspiration in all patients, and successful treatment with needle aspiration was done in 12 (86.0%) of 14 patients. Treatment with needle aspiration failed in two patients (14.0%), with the development of perirectal abscess after transrectal needle aspiration in one patient (patient 7) (Fig. 5) and a small aspirate volume in another patient (patient 8). The former patient was treated with perineal incision and drainage, and the latter with transurethral resection. Treatment with needle aspiration via transrectal approach was completed in a procedure in eight (67.0%) of 12 patients. The remaining four patients (33.0%) needed a repeat procedure, these treatments being a second procedure in three patients (patient 11, 13, and 14) and a third procedure in one patient (patient 1). The amount of drained pus ranged from 1 to 39 ml (mean, 12.0 ml). After the TRUS-guided needle aspiration, antibiotics therapy was initiated in all patients, intravenously in 14 patients (cephalosporin, third-generation cephalosporin, and third-generation quinolone) and intramuscularly in 10 patients (aminoglycoside). TRUS-guided aspiration allowed us to identify Escherichia coli in three patients, Staphylococcus aureus in four patients, Pseudomonas aeruginosa in two patients, and Klebsiella pneumoniae in one patient. In four patients, the same pathogen was the cause of both urinary tract infection and PA. In the remaining four patients, the organism responsible was not confirmed (Table 2). Complication associated with needle aspiration via transrectal route, which consisted of perirectal abscess formation (Fig. 5), developed in one patient (patient 7). Hospital stays ranged between 8 and 21 days (mean, 13.6 days). On followup TRUS, no remaining abscess pockets were found within the prostate in any of the cases. After 1 year, PA recurred in one case (patient 3). J Ultrasound Med 19:609–617, 2000 LIM ET AL DISCUSSION PA is an unusual condition. Such abscesses usually are complications of acute bacterial prostatitis that either has not been treated or has been inappropriately treated.2,9,10 Delay in diagnosis can have grave sequelae, including a rupture of the abscess into the ischiorectal fossa or into the perivesical space with associated morbidity and 613 death.1,8,9,11 Since the advent of antibiotic therapy, the prevalence of PA has decreased, and the type of organisms responsible for the development of PA has changed.2–4,7 The prevalence of PA is about 0.5% of all prostatic disease.2 In the preantibiotic era, Neisseria gonorrheae was the primary organism, responsible in 75% of the cases. In the antibiotic era, gram-negative bacilli (chiefly E. coli) have caused about 60 to 80% of cases. Other significant Table 3: TRUS Findings in Patients with Prostatic Abscesses (n = 14) TRUS Appearance of Lesion Patient Number of Lesions Mean Diameter (cm) Location Echogenicity Septum or Solid Portion Margin Perilesional Change 1 2 2.6, 3 Both sides inner and outer gland Inhomogeneous hypoechoic + Well-defined, thick wall Periprostatic extension 2 2 3.4, 2.7 Both sides inner and outer gland Inhomogeneous hypoechoic + Poorly defined 3 2 2.3, 3.2 Both sides inner gland Inhomogeneous hypoechoic – Well-defined, thick wall Perilesional hypoechoic area 4 2 1.9, 1.7 Both sides outer gland Inhomogeneous hypoechoic + Poorly defined Perilesional hypoechoic area, periprostatic extension 5 1 2.2 Left inner gland Inhomogeneous hypoechoic + Well-defined, thick wall Perilesional hypoechoic area 6 1 1.5 Right outer gland Inhomogeneous hypoechoic – Well-defined, thick wall Perilesional hypoechoic area 7 1 2.2 Left outer gland Inhomogeneous hypoechoic + Well-defined, thick wall Perilesional hypoechoic area 8 2 2.6, 1.7 Both sides inner and outer gland Inhomogeneous hypoechoic + Well-defined, thick wall Perilesional hypoechoic area, periprostatic extension 9 2 1.3, 1.2 Both sides outer gland Inhomogeneous hypoechoic – Well-defined, thick wall Perilesional hypoechoic area 10 1 3.4 Inner and outer gland Inhomogeneous hypoechoic – Well-defined, thick wall 11 3 1.8, 3.5, 1.8 Both sides inner and outer gland Inhomogeneous hypoechoic + Poorly defined Perilesional hypoechoic area 12 1 2.4 Left outer gland Inhomogeneous hypoechoic + Well-defined, thick wall Perilesional hypoechoic area, periprostatic extension 13 1 2.7 Right inner and outer gland Inhomogeneous hypoechoic + Well-defined, thick wall Perilesional hypoechoic area, periprostatic extension 14 1 3.0 Left inner gland Inhomogeneous hypoechoic + Well-defined, thick wall Periprostatic extension 614 TREATMENT OF PROSTATIC ABSCESS J Ultrasound Med 19:609–617, 2000 A B Figure 2 62 year old man with acute urinary retention. Transverse (A) and left longitudinal (B) sonograms show abscesses as hypoechic areas with poorly defined margin in both the inner and outer portions of the gland (arrows, asterisks). Left longitudinal sonogram shows periprostatic extension of prostatic abscess (arrowheads). pathogens include Pseudomonas species, staphylococci, and occasionally obligate anaerobic bacteria.2–4,6,7 The pathogenesis of a PA has been thought to involve two distinct mechanisms. The first mechanism is infected urine reflux, which occurs in older persons with preexisting bladder outlet obstruction. This is the most common mechanism, and the most frequent microorganisms responsible are Escherichia coli or other coliform bacteria. The second mechanism is hematogenous dissemination from a primary focus. This mechanism involved a much smaller group of patients, and the most common microorganism is Staphylococcus aureus.2,3,5,9 In view of the mechanisms involved, predisposing factors for a PA include bladder outlet obstruction, urethral instrumentation, and carcinoma of the prostate; further predisposing factors include systemic diseases, such as diabetes, liver disease, chronic renal failure, acquired immunodeficiency syndrome, and immunosuppressive therapy.2,3,5,6,9 The signs and symptoms of PA included, in order of frequency, acute urinary retention, fever, dysuria, urinary frequency, perineal pain, hematuria, urethral discharge, and pain in the lower back. The classic finding on a digital rectal examination of a tender, fluctuant mass often is exceptional and not the Figure 3 70 year old man with hematuria and perineal pain. A, Transverse sonogram shows the abscess as an inhomogeneous hypoechoic area with well-defined margin in the inner part of the gland (asterisk). Note perilesional hypoechoic area (arrows). B, Color Doppler sonogram shows no blood flow within the hypoechoic area (asterisk). Note diffusely increased blood flow at the perilesional hypoechoic area, indicating inflammatory change. A B J Ultrasound Med 19:609–617, 2000 LIM ET AL 615 A B Figure 4 59 year old man with diabetes who had urinary frequency and dysuria. A, Longitudinal sonogram shows abscess as hypoechoic area. Texture is complex because of presence of fluid collection with debris and septation. B, CT scan shows multiple areas of low attenuation in the prostate with periprostatic extension (arrowheads). rule.1–4,6 Because signs, symptoms, and physical findings of PA are similar to those of acute bacterial prostatitis, the diagnosis of PA often is difficult on clinical basis alone.2,5,6,8,10 However, it is very important to distinguish between acute prostatitis and PA, since the therapeutic approach for each is different. From this point of view, prostatic imaging (TRUS, CT, MR imaging) is important in the diagnosis and management of PA. Of these types of prostatic imaging, TRUS is the most widely used technique in the diagnosis of PA and in the guide for percutaneous aspiration and drainage. It also is useful in evaluation of response to treatment.1,2,6,8,9 The most common TRUS finding of PA was one or more hypoechoic areas with well-defined and thick walls, seen in 79.0% of all patients. A hypoechic area with poorly defined walls was seen less frequently. Other conditions that may have a similar appearance to that of PA on TRUS are neoplastic processes, cystic lesions, and granulomas.1,2,7,10,19 However, the TRUS appearance of PA was quite characteristic and could be differentiated from that of other conditions. Reported criteria discriminating PA from prostate cancer include the following: (1) prostate carcinoma usually appears small and is more easily distinguishable from the surrounding gland, whereas PA Figure 5 75 year old man with indwelling catheter because of neurogenic bladder. A perirectal abscess developed after needle aspiration of PA. A, Transverse sonogram shows abscess as an inhomogeneous hypoechoic area with periprostatic extension in the apex portion of the left outer gland (asterisk). B, After treatment of the PA with TRUS-guided needle aspiration, the patient complained of fever and perineal pain. Transverse sonogram shows perirectal abscess as a complication of needle aspiration (arrows). A B 616 TREATMENT OF PROSTATIC ABSCESS occupies a large area of one or both glands; (2) carcinoma is found more frequently in the peripheral zone of the prostate, whereas PA is usually located in the central gland; (3) PA generally appears as a wider hypoechoic area and is less easily definable during its initial phase; (4) color and power Doppler sonographic examinations show a high perilesional vascularity that is absent within the tumor.1,7,19 Of these criteria, the location of the lesion may not be helpful in differentiating PA from prostate cancer, because PA can occur in both inner and outer gland. In our study, the PA was located in both the outer and inner gland in six patients, in the outer gland in five patients, and in the inner gland in three patients. In addition to high perilesional vascularity, our study showed a diffusely increased blood flow at the remaining portion of the prostate on color and power Doppler sonography. This was thought to represent an inflammatory reaction. After the diagnosis of PA is made, therapy consists of adequate drainage of the abscess and administration of pathogen-specific antimicrobial agents.6 Surgical drainage is accepted as the most important step in the treatment of a PA. However, the exact method of drainage remains somewhat controversial. Drainage techniques for PA included perineal incision and drainage, transurethral unroofing and resection into the abscess cavity, blind aspiration, and percutaneous transperineal drainage.1,3–7 Because perineal incision could cause impotence due to nerve damage, perineal incision and drainage is now seldom used.1,6 Although transurethral resection not only has the potential of causing the hematogenous spread of infectious organisms but also could have potential complications, such as retrograde ejaculation, urethral stenosis, or urinary incontinence,1,2 it is frequently used in the treatment of a PA in many institution.3,4,6 Some investigators reported the placement of a transperineal drainage catheter under TRUS-guidance as the treatment method for a PA.1,3,7 Percutaneous catheter drainage under radiologic guidance is an accepted method for draining abdominal abscesses and other fluid collections. The safety and efficacy of this procedure are well established. In percutaneous drainage, the principle is that, in addition to the aspiration of all drainable pus, a catheter should be left in the abscess cavity until all drainage cease and the space becomes obliterated.3,5,6,12–16 Initially, a transperineal route is preferred for the percutaneous drainage of PA, because this approach could avoid rectourethral fistula formation and fecal contamination of the abscess cavity.18,20 In contrast to percutaneous catheter drainage of abdominal abscesses, transperineal drainage of a PA may result in a painful and prolonged catheter drainage procedure. J Ultrasound Med 19:609–617, 2000 Few reports have been published showing that TRUS-guided needle aspiration via transrectal route could produce a cure in the treatment of PA.2,7,18 The rationale for this regimen is that emptying the collection is likely to a pressure reduction within the PA, thereby resulting in easy intracavitary antibiotic inflow.2 Collado and coworkers2 reported on results in the largest series, 24 patients treated with transrectal needle aspiration and adjuvant antibiotic therapy. Results of PA needle aspiration in these 24 patients were successful in 20 patients (83.3%); only two patients required second procedures.2 In our experience, 12 (85.7%) of 14 cases were successfully treated with needle aspiration; four cases needed a repeat procedure. In our study, we did not place a catheter for transrectal drainage. Although catheters provide continuous drainage of pus, thereby resulting in complete evacuation of pus,21 there are several problems in transrectal drainage: (1) the catheter may be uncomfortable, (2) prevention of dislodgment may be a problem in management, and (3) restriction in ambulation may be advisable.22 The advantages of transrectal needle aspiration using TRUS-guidance include (1) the trajectory of the needle is shorter because of close contact between the prostate and the probe; (2) direct access through the rectal wall minimizes bleeding, injury to adjacent organs, and spread of infection; (3) this approach is more comfortable for the patient than the transperineal approach, which is more painful.2,17 In our study, seven patients had multiple abscesses. With a repositioning of the needle, it is possible to aspirate multiple abscesses in different locations. We performed more than one procedure in four patients (two procedures in three patients and three procedures in one patient). Because of thick viscous pus, initial aspirate volumes in these four patients were small in amount. However, in these four patients, repeat aspiration after an interval of 3 to 7 days successfully removed the predicted volume of pus. Thus, we considered that the treatment in these subjects was successful treatment. Although some investigators have used saline solution irrigation or intraprostatic infiltration of antibiotic to improve outcome,2,5,17,23 we did not use it in our study. Without saline solution irrigation or antibiotic intraprostatic infiltration, we obtained good results in our study; therefore, we do not think either of these is indicated. In conclusion, TRUS is important in the diagnosis of PA, in guidance for aspiration, and in drainage of the PA. TRUS-guided transrectal needle aspiration could be an effective method for treating PA that does not require catheter placement or prolonged drainage. J Ultrasound Med 19:609–617, 2000 REFERENCES 1. Barozzi L, Pavlica P, Menchi I, et al: Prostatic abscess: Diagnosis and treatment. AJR 170:753, 1998 2. Collado A, Palou J, Garcia-Penit J, et al: Ultrasoundguided needle aspiration in prostatic abscess. Urology 53:548, 1999 LIM ET AL 617 14. Bennett JD, Kozak RI, Taylor BM, et al: Deep pelvic abscesses: Transrectal drainage with radiologic guidance. Radiology 185:825, 1992 15. Mauro MA, Jaques PF, Mandell VS, et al: Pelvic abscess drainage by the transrectal catheter approach in men. AJR 144:477, 1985 16. Clark RA, Towbin R: Abscess drainage with CT and ultrasound guidance. Radiol Clin North Am 21:445, 1983 3. Meares EM Jr: Prostatic abscess. J Urol 136:1281, 1986 4. Trauzzi SJ, Kay CJ, Kaufman DG, et al: Management of prostatic abscess in patients with human immunodeficiency syndrome. 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