Benign prostatic hyperplasia
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Steven C. Campbell, M.D., Ph.D.
Synonyms and keywords: Hyperplasia of the Postate; Prostate hyperplasia, benign; prostatic hypertrophy; adenofibromatous hypertrophy of prostate; benign prostatic hypertrophy
Overview
Steven C. Campbell, M.D., Ph.D.
Overview
Benign prostatic hyperplasia refers to the increase in size of the prostate in middle-aged and elderly men. To be accurate, the process is one of hyperplasia rather than hypertrophy, but the nomenclature is often interchangeable, even amongst urologists. It is characterized by hyperplasia of prostatic stromal and epithelial cells, resulting in the formation of large, fairly discrete nodules in the periurethral region of the prostate. When sufficiently large, the nodules compress the urethral canal to cause partial, or sometimes virtually complete, obstruction of the urethra which interferes the normal flow of urine. It leads to symptoms of urinary hesitancy, frequent urination, increased risk of urinary tract infections and urinary retention. Although prostate specific antigen levels may be elevated in these patients, because of increased organ volume and inflammation due to urinary tract infections, BPH is not considered to be a premalignant lesion.
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Historical Perspective
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Pathophysiology
Steven C. Campbell, M.D., Ph.D.
Pathophysiology
Androgens (testosterone and related hormones) are considered to play a permissive role in BPH by most experts. This means that androgens have to be present for BPH to occur, but do not necessarily directly cause the condition. This is supported by the fact that castrated boys do not develop BPH when they age, unlike intact men. Additionally, administering exogenous testosterone is not associated with a significant increase in the risk of BPH symptoms. Dihydrotestosterone (DHT), a metabolite of testosterone is a critical mediator of prostatic growth. DHT is synthesized in the prostate from circulating testosterone by the action of the enzyme 5α-reductase, type 2. This enzyme is localized principally in the stromal cells; hence, these cells are the main site for the synthesis of DHT.
DHT can act in an autocrine fashion on the stromal cells or in paracrine fashion by diffusing into nearby epithelial cells. In both of these cell types, DHT binds to nuclear androgen receptors and signals the transcription of growth factors that are mitogenic to the epithelial and stromal cells. DHT is 10 times more potent than testosterone because it dissociates from the androgen receptor more slowly. The importance of DHT in causing nodular hyperplasia is supported by clinical observations in which an inhibitor of 5α-reductase is given to men with this condition. Therapy with 5α-reductase inhibitor markedly reduces the DHT content of the prostate and in turn reduces prostate volume and, in many cases, BPH symptoms.
There is growing evidence that estrogens play a role in the etiology of BPH. This is based on the fact that BPH occurs when men generally have elevated estrogen levels and relatively reduced free testosterone levels, and when prostate tissue becomes more sensitive to estrogens and less responsive to DHT. Cells taken from the prostates of men who have BPH have been shown to grow in response to high estradiol levels with low androgens present. Estrogens may render cells more susceptible to the action of DHT.
On a microscopic level, BPH can be seen in the vast majority of men as they age, particularly over the age of 70 years, around the world. However, rates of clinically significant, symptomatic BPH vary dramatically depending on lifestyle. Men who lead a western lifestyle have a much higher incidence of symptomatic BPH than men who lead a traditional or rural lifestyle. This is confirmed by research in China showing that men in rural areas have very low rates of clinical BPH, while men living in cities adopting a western lifestyle have a skyrocketing incidence of this condition, though it is still below rates seen in the West.
Much work remains to be done to completely clarify the causes of BPH.
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Causes
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Drug Induced
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Differentiating Benign Prostatic Hyperplasia from other Diseases
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Epidemiology and Demographics
Steven C. Campbell, M.D., Ph.D.
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Overview
More than half of the men in the United States between the ages of 60 and 70 and as many as 90% between the ages of 70 and 90 have symptoms of BPH. For some men, the symptoms may be severe enough to require treatment.
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Risk Factors
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Screening
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Natural History, Complications and Prognosis
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Complications
Men who have had long-standing BPH with a gradual increase in symptoms may develop:
- Sudden inability to urinate
- Urinary tract infections
- Urinary stones
- Damage to the kidneys
- Blood in the urine
Even after surgical treatment, a recurrence of BPH may develop over time.
Prognosis
Treatments options as stated above are likely to relieve symptoms. Surgery is slightly more successful in relieving symptoms, but the risk of complications is greater.
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Diagnosis
Diagnosis
History and Symptoms | Physical Examination | Laboratory Findings | Ultrasound | Other Imaging Findings | Other Diagnostic Studies
Treatment
Treatment
Medical Therapy | Surgery | Primary Prevention | Secondary Prevention | Cost-Effectiveness of Therapy | Future or Investigational Therapies
Related chapters
Related chapters
- Prostate
- Prostate cancer
- Prostate specific antigen
- Prostatectomy
- Urinary retention
- Uvula of urinary bladder
Template:Diseases of the pelvis, genitals and breasts
de:Benigne Prostatahyperplasie it:Ipertrofia prostatica benigna ka:პროსტატის კეთილთვისებიანი ჰიპერპლაზია nl:Benigne prostaathypertrofie fi:Eturauhasen liikakasvu
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