eMedicine Specialties > Urology > Infections and Related Inflammatory Conditions

Prostatitis, Tuberculous

Author: Vernon M Pais Jr, MD, Assistant Professor, Department of Surgery, Section of Urology, Dartmouth Medical School
Coauthor(s): Levi A Deters, MD, Staff Physician, Department of Urology, Dartmouth Hitchcock Medical Center; Jason R Bylund, MD, Resident, Division of Urology, University of Kentucky; Andrew A Wagner, MD, Staff Physician, Department of Surgery, Division of Urology, University of Massachusetts Medical Center
Contributor Information and Disclosures

Updated: Jun 26, 2009

Introduction

Background

Tuberculosis (TB) has plagued humankind since antiquity. The effects of TB have been noted in skeletal remains from 4000 BC, and both Hippocrates and Galen described TB's clinical manifestations; however, prostatic TB was not described until the turn of the 20th century.

The most common site of TB infection is the pulmonary tract; however, the genitourinary tract is the most common extrapulmonary site of TB infection (33% of cases). Only 20% of TB prostatitis cases are accompanied by underlying pulmonary infection.1

Despite optimistic predictions on the eradication of TB in developed nations, the disease continues to pose a major worldwide health problem. In 2006, the World Health Organization reported that more than 2 billion people, roughly one third of the world’s population, are infected with TB and a reported 1.7 million deaths per year are due to TB. Developing nations continue to carry a burden of the disease (83% of total cases), with 9.6 million new cases of TB reported worldwide during 2006. To compound the problem, in both developing and industrialized nations, rates of active TB associated with HIV infection are increasing (8% of total), and the incidence of multidrug-resistant TB is also increasing, with a reported 0.5 million cases during 2006.2

Pathophysiology

The causative agent in tuberculous prostatitis is Mycobacterium tuberculosis, a strictly aerobic nonmotile bacterium. The bacterium grows slowly, dividing only once every 24 hours, and is capable of surviving within immune cells after phagocytosis. Generally, tuberculous prostatitis results from hematogenous dissemination of the mycobacteria from the site of the primary infection. Theories of descending spread via infected urine have been abandoned, largely in light of animal studies demonstrating hematogenous spread and the scarcity of prostatic urethral TB in association with prostatic parenchymal TB.

Frequency

United States

Large autopsy studies from the first half of the 20th century report a 10%-12% incidence of prostatic involvement in men with TB.

International

Direct data are lacking, although extrapolation of the US autopsy data suggests that 10%-12% of men with TB might have prostatic involvement. More recent small series suggest a lower rate of clinically detected prostatic TB.

Mortality/Morbidity

  • Mortality directly attributable to prostatic TB has not been reported in the recent literature. A case report described 2 patients with HIV infection who died of disseminated TB during hospitalization. Unsuspected tuberculous prostatic abscesses were noted in both patients during the postmortem examination.
  • Male factor infertility, which manifests as decreased ejaculate volume, oligospermia, azoospermia, and leukocytospermia, has been observed in association with tuberculous prostatitis. A perineal urinary fistula may result from tubercular cavern formation within or behind the prostate. Reports note perineal swelling, pain, and discharge preceding the development of the urinary fistula. Prostatic tuberculous abscess formation has been noted, particularly in men with AIDS.

Race

Contemporary studies have not addressed racial distributions of tuberculous prostatitis. Autopsy data published in 1949 evaluated prostatic TB in white and nonwhite patients. Of 169 nonwhite patients with TB, 18 (10.7%) had prostatic involvement during autopsy, compared with 50 of 660 (7.6%) white patients.

Sex

Prostatic TB affects only males.

Age

In 1937, Moore presented the age distribution of 243 cases of prostatic TB. Seventy-nine percent of patients were younger than 50 years. Moore describes this as "a disease of young adults."3 The recent literature is unable to offer as large a view of the age distribution.

Kostakopoulos et al (1998) presented 5 cases of unsuspected prostatic TB, all in patients aged 60-71 years.4 Although this starkly contrasts with Moore's earlier data, all 5 cases were incidental findings at the time of transurethral resection of the prostate (TURP), and they do not necessarily reflect the age at which the disease first developed.

Over the last 15 years, case reports of prostatic TB in immunocompetent men note patient ages of 26-85 years. Reported cases of prostatic TB in men with HIV infection document presentation in men aged 30-47 years. Most recently, Kulchavenya and Khomyakov reported on a series of 58 Siberian men with prostatic TB; their mean age was 49 years.5

Clinical

History

  • The often-incidental finding of tuberculosis (TB) in TURP chips suggests that many men may not have symptoms attributable to prostatic TB.
  • Nonspecific symptoms, including irritative voiding, may be the only complaints. Of men with prostatic TB, 50% have dysuria and 40% have perineal pain. Renal TB, which is a common comorbidity, may manifest as flank pain. Significant differential diagnostic overlap requires maintaining a high index of suspicion for prostatic TB, particularly in men with a history of exposure to or infection with TB.
  • Patients may present with male factor infertility, a well-described complication of prostatic TB.
  • Sterile urethral discharge and terminal hematuria may herald tuberculous prostatitis.
  • Perineal pain, swelling, and drainage can account for a less common but more overt presentation. Perineal urinary fistula has been reported.
  • The most dramatic presentations of prostatic TB may be those in men with AIDS. To date, 6 cases of tuberculous prostatic abscesses have been reported in men with HIV infection. Unlike the more insidious presentations noted in immunocompetent men, these patients presented with fever, perineal pain, and urinary hesitancy; 2 of the patients also presented with mental status changes.

Physical

  • Most patients with prostatic TB in contemporary series have a prostate that may be hard, irregular, nodular, or granular.
  • In patients with a prostatic tuberculous abscess, a soft fluctuant mass has been noted.
  • Tenderness varies with the acuity of the process.
  • Prostatic TB should be suspected in patients who have a draining perineal fistula.

Causes

  • Prior infection with TB is the most important risk factor. Historically, 10%-12% of men with TB had pathologic evidence of prostatic involvement during autopsy.
  • HIV infection increases the risk for active TB and has been suggested to increase the risk for reactivation of dormant foci.
  • Prolonged steroid use and immunosuppressive therapy may increase the risk of reactivation of dormant foci.
  • Case reports have described prostatic TB as a complication of intravesical bacillus Calmette-Guérin immunotherapy.6

More on Prostatitis, Tuberculous

Overview: Prostatitis, Tuberculous
Differential Diagnoses & Workup: Prostatitis, Tuberculous
Treatment & Medication: Prostatitis, Tuberculous
Follow-up: Prostatitis, Tuberculous
References

References

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Further Reading

Keywords

tuberculous prostatitis, tuberculosis, TB, prostatic TB, prostatic tuberculosis, consumption, phthisis, Mycobacterium tuberculosis, M tuberculosis, prostatic urethral tuberculosis, prostatic urethral TB, prostatic parenchymal tuberculosis, prostatic parenchymal TB, tuberculous prostatic abscess, genitourinary tuberculosis, GU tuberculosis, genitourinary TB

Contributor Information and Disclosures

Author

Vernon M Pais Jr, MD, Assistant Professor, Department of Surgery, Section of Urology, Dartmouth Medical School
Vernon M Pais Jr, MD is a member of the following medical societies: Alpha Omega Alpha, American Urological Association, Endourological Society, Sigma Xi, and Society of Laparoendoscopic Surgeons
Disclosure: Nothing to disclose.

Coauthor(s)

Levi A Deters, MD, Staff Physician, Department of Urology, Dartmouth Hitchcock Medical Center
Disclosure: Nothing to disclose.

Jason R Bylund, MD, Resident, Division of Urology, University of Kentucky
Disclosure: Nothing to disclose.

Andrew A Wagner, MD, Staff Physician, Department of Surgery, Division of Urology, University of Massachusetts Medical Center
Andrew A Wagner, MD is a member of the following medical societies: American Urological Association
Disclosure: Nothing to disclose.

Medical Editor

Richard A Santucci, MD, FACS, Chief of Urology, Detroit Receiving Hospital; Specialist-in-Chief of Urology, Detroit Medical Center; Chief of Urologic Trauma Surgery, Sinai Grace Hospital; Director, The Center for Urologic Reconstruction; Clinical Professor of Urology, Michigan State College of Medicine
Richard A Santucci, MD, FACS is a member of the following medical societies: American College of Surgeons, American Urological Association, and Société Internationale d'Urologie (International Society of Urology)
Disclosure: Nothing to disclose.

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: eMedicine Salary Employment

CME Editor

J Stuart Wolf Jr, MD, FACS, David A Bloom Professor of Urology, Director of Division of Minimally Invasive Urology, Department of Urology, University of Michigan
J Stuart Wolf Jr, MD, FACS is a member of the following medical societies: American College of Surgeons, American Urological Association, Catholic Medical Association, Endourological Society, Society for Urology and Engineering, Society of Laparoendoscopic Surgeons, Society of University Urologists, and Society of Urologic Oncology
Disclosure: Terumo Corporation Consulting fee Consulting; Omeros Corporation Consulting fee Consulting

Chief Editor

Edward David Kim, MD, FACS, Professor of Surgery, Division of Urology, University of Tennessee Graduate School of Medicine; Consulting Staff, University of Tennessee Medical Center
Edward David Kim, MD, FACS is a member of the following medical societies: American College of Surgeons, American Society for Reproductive Medicine, American Society of Andrology, American Urological Association, and Tennessee Medical Association
Disclosure: Lilly Consulting fee Consulting; Astellas Consulting fee Speaking and teaching; Indevus Consulting fee Speaking and teaching

 
 
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