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Eble JN, Sauter G., Epstein JI, Sesterhenn IA - iarc

Eble JN, Sauter G., Epstein JI, Sesterhenn IA - iarc

Eble JN, Sauter G., Epstein JI, Sesterhenn IA - iarc

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A<br />

Fig. 3.12 A Organ-confined adenocarcinoma of the prostate extending to edge of gland.<br />

B Adenocarcinoma of the prostate with focal extra-prostatic extension.<br />

B<br />

Fig. 3.15 Extraprostatic extension by prostatic adenocarcinoma,<br />

with tracking along nerve, into<br />

periprostatic adipose tissue.<br />

cases of obvious carcinoma, there may<br />

be cells that closely mimic basal cells.<br />

These cells when labeled with basal cell<br />

specific antibodies are negative and represent<br />

fibroblasts closely apposed to the<br />

neoplastic glands. Conversely, basal<br />

cells may not be readily recognized in<br />

benign glands without the use of special<br />

studies. The histopathology of prostatic<br />

cancer, and its distinction from benign<br />

glands, rests on a constellation of architectural,<br />

nuclear, cytoplasmic, and intraluminal<br />

features. With the exception of<br />

three malignant specific features listed at<br />

the end of this section, all of the features<br />

listed below, while more commonly seen<br />

in cancer, can also be seen in benign<br />

mimickers of cancer.<br />

A<br />

Fig. 3.13 A Intraprostatic lymphovascular space invasion by prostatic adenocarcinoma. B Ejaculatory duct<br />

invasion by prostatic adenocarcinoma, with duct wall invasion, with sparing of ejaculatory duct epithelium<br />

and lumen.<br />

Fig. 3.14 Limited adenocarcinoma of the prostate on needle biopsy.<br />

tinguish them from benign prostatic<br />

glands, to poorly differentiated tumours,<br />

difficult to identify as being of prostatic<br />

origin. A feature common to virtually all<br />

prostate cancers is the presence of only<br />

a single cell type without a basal cell<br />

layer. Benign prostate glands, in contrast,<br />

contain a basal cell layer beneath<br />

the secretory cells. The recognition of<br />

basal cells on hematoxylin and eosin<br />

stained sections is not straightforward. In<br />

B<br />

Architectural features<br />

Benign prostatic glands tend to grow<br />

either as circumscribed nodules within<br />

benign prostatic hyperplasia, radiate in<br />

columns out from the urethra in a linear<br />

fashion, or are evenly dispersed in the<br />

peripheral zone {1685}. In contrast,<br />

gland-forming prostate cancers typically<br />

contain glands that are more crowded<br />

than in benign prostatic tissue, although<br />

there is overlap with certain benign mimickers<br />

of prostate cancer. Glands of adenocarcinoma<br />

of the prostate typically<br />

grow in a haphazard fashion. Glands oriented<br />

perpendicular to each other and<br />

glands irregularly separated by bundles<br />

of smooth muscle are indicative of an<br />

infiltrative process. Another pattern characteristic<br />

of an infiltrative process is the<br />

presence of small atypical glands situated<br />

in between larger benign glands. With<br />

the loss of glandular differentiation and<br />

the formation of cribriform structures,<br />

fused glands, and poorly formed glands,<br />

the distinction between benign glands<br />

based on the architectural pattern<br />

becomes more apparent. Tumours composed<br />

of solid sheets, cords of cells, or<br />

isolated individual cells characterize<br />

undifferentiated prostate cancer. These<br />

architectural patterns are key components<br />

to the grading of prostate cancer<br />

(see Gleason grading system).<br />

170 Tumours of the prostate

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