# Pathology

Pathology

BPH a ff ects both glandular epithelium and connective tissue stroma to variable degrees. BPH typically a ff ects the submucous group of glands in the transitional zone, forming a nodular enlargement. Eventually , this overgrowth compresses the peripheral zone glands into a false capsule and causes the appearance of  the typical ‘lateral’ lobes. When BPH a ff ects the central zone glands, a ‘middle’ lobe develops that projects up into the bladder within the internal sphincter ( Figure 84.1 ). 

Which investigations are appropriate for benign and
•
malignant conditions of the prostate
Clinical staging of carcinoma of the prostate and how
•
staging contributes to the complex decision making
Right half of bladder
Enlargement of
lateral lobe of
prostate
Prostatic
urethra
Hypertrophy
of trigone
Enlargement of
Posterior lobe
median lobe of
of prostate
prostate
Figure 84.1
Diagram of late-stage bladder out
/f_l
ow obstruction show
-
ing enlargement of the prostate from benign prostatic hyperplasia,
trabeculation of the bladder with smooth muscle hypertrophy and
/f_i
brosis.

Pathology

Serial sections of prostates obtained at routine necropsy demonstrate prostate carcinoma in 25% of  men between 50 and 65 years of  age. The incidence in men over 80 years is in the region of  70%. Most of  these neoplasms are tiny and (if life had continued) might have remained latent for years. Most men die with the prostate cancer rather than because of  cancer. The following types of  prostate cancer occur: /uni25CF microscopic latent cancer found on autopsy or at cysto prostatectomy; /uni25CF tumours found incidentally during TURP (T1a and T1b) or following screening by PSA measurement (T1c); /uni25CF early , localised prostate cancer (T2); /uni25CF locally advanced and high-risk prostate cancer (T3 and T4); /uni25CF metastatic disease, which may arise from a clinically evi dent tumour (T2, T3 or T4) or from an apparently benign gland (T0, T1) (i.e. occult prostate cancer). It should be noted that only the last two groups cause symp toms, and such tumours are not curable. Only screening or the trea tment of  incidentally found tumours or early prostate cancer (T1 and T2) can result in cure of  the disease. The prob lem is that many suc h tumours would never progress during the patient’s lifetime and only a few will grow and metastasise; herein lies the problem with prostate cancer.