Jb. Brennick et al., LIPOFUSCIN PIGMENTATION (SO-CALLED MELANOSIS) OF THE PROSTATE, The American journal of surgical pathology, 18(5), 1994, pp. 446-454
Although intraepithelial pigment in the prostate gland has been termed
melanosis, the nature of the pigment is not entirely clear, and many
pathologists are not aware of its existence. We examined 863 hematoxyl
in and eosin (H + E) stained slides from 150 surgical specimens of pro
state (69 needle biopsies, 66 transurethral resections, 14 radical pro
statectomies, and 1 suprapubic prostatectomy) from 149 patients (age r
ange, 47 to 90 years; mean 70 years) in an effort to characterize this
pigment. The 1-3 mu m in diameter, predominantly subnuclear, yellow-b
rown to gray-brown granules with a dark blue rim (by H + E) stained po
sitively with Fontana-Masson, periodic acid-Schiff with diastase, Cong
o red, luxol fast blue, and oil-red-O and exhibited yellow autofluores
cence consistent with lipofuscin. H + E stained slides revealed pigmen
t in the benign epithelium in 86 of 150 cases (57%), within stromal ma
crophages in eight cases, and in atypical epithelium in two cases of h
igh-grade prostatic intraepithelial neoplasia. Ten cases of invasive a
denocarcinoma without recognizable pigment in H + E stained sections w
ere stained by the Fontana-Masson technique, and pigment was identifie
d in malignant epithelium in three of these cases. Ultrastructural exa
mination of intraepithelial pigment in KII-fixed tissue from three rad
ical prostatectomy specimens demonstrated the typical appearance of li
pofuscin. Although intraepithelial pigment in prostatic biopsy or rese
ction specimens is usually considered characteristic of seminal vesicl
e epithelium, our study demonstrates that lipofuscin is commonly prese
nt in epithelial cells of benign prostatic hyperplasia and less freque
ntly in those of prostatic intraepithelial neoplasia and adenocarcinom
a. The recognition of this pigment is important in preventing diagnost
ic confusion with seminal vesicle epithelium and with melanocytic lesi
ons.