Prostate gland
The prostate gland adds juice to the sperm. In old men it creates lotsa problems... nodular hyperplasia (commonly called BPH or benign prostatic hyperplasia) and cancer (adenocarcinoma).
Normal
Prostate
Anatomy
Divided into three zones:[1]
- Peripheral zone - posterior aspect, palpable with digit.
- Classic location for cancer.
- Central zone - considered resistant to disease.
- Transition zone - usual location for nodular hyperplasia.
Histology
- Glands have two cell layers (similar to glands in breast).
- Second cell layer may be difficult to see (like in breast).
- Epithelium in glands is "folded" or "tufted".
- Very important - helps on differentiate from Gleason pattern 3.
- Luminal epithelium often clear cytoplasm.
- Single nucleus.
Benign normal:
- Corpora amylacea.
- Round/ovoid-eosinophilic bodies -- with laminations (layered appearance).
- In gland lumina.
- Usually in benign glands - but cannot be used to exclude cancer.[2]
- Very common.
- These should be differentiated from eosinophilic proteinaceous debris - which is associated with cancer.
Negatives:
- No nucleoli present (if you see nuclei think: cancer, HGPIN, reactive changes, basal cell hyperplasia).
- No mitoses - these are uncommon... even in high grade prostate cancer.
Notes:
- Tufted epithelium is a strong indicator of benignancy; however two uncommon prostate cancer typically have tufted epithelium:
- Pseudohyperplastic adenocarcinoma.
- Foamy gland carcinoma.
Images:
- Benign prostate with corpora amylacea - low mag. (WC).
- Benign prostate with corpora amylacea - high mag. (WC).
IHC of normal prostate
Normal prostate:
- AMACR -ve (mark epithelial cells).
- CK5/6 +ve,[3] p63 +ve, HMWCK +ve (mark basal cells).
- PSA (prostate-specific antigen) +ve, PSAP (prostatic-specific acid phosphatase) +ve.
Other accessory glands
Bulbourethral gland
- AKA Cowper's gland.
- Mucinous glands at the apex of the prostate.
- Resemble (mucinous) salivary glands.[4]
Image: Mucinous/serous salivary gland (duke.edu).
Seminal vesicles
- Fern-like architecture - epithelial component clustered closely, looks like it connects.
- Epithelium surrounded by a thick layer of muscle (>10 cells across ~80 microns).
- Lipofuscin (coarse cytoplasmic yellow granules approximately 1-2 micrometers) - key feature.
- Nucleoli - common.
- Nuclear inclusions - common.
Notes:
- The ejaculatory ducts have the same epithelium as the seminal vesicles.[5]
Images:
- SV - showing fern-like architecture (WC).
- SV - looking vaguely like to prostate adenocarcinoma (WC).
- SV - looks a bit like prostate but lumina too big (WC).
- SV (udel.edu).
Specimens
- Prostate core biopsy - done transrectal.
- Prostate chips (from a transurethral resection of the prostate, abbreviated TURP) - usu. done for nodular hyperplasia of the prostate gland; may be done in the context of obstructing cancer.
- Radical prostatectomy - includes the seminal vesicles.
- Radical cystoprostatectomy - includes the urinary bladder and seminal vesicles.[6]
Common diagnoses
- Benign.
- Atrophy - may resemble adenocarcinoma - typically not reported.
- Adenosis - may resemble adenocarcinoma - typically not reported.
- Prostate adenocarcinoma.
- Most common Grade is 3+3=6.
- HGPIN (high-grade prostatic intraepithelial neoplasia) - prostate adenocarcinoma precursor lesion.
- ASAP (atypical small acinar proliferation) - used if you have a few abnormal appearing glands... but can't decide between prostate adenocarcinoma & benign.
- Chronic inflammation.
- Acute inflammation - can result in an elevated PSA and may have prompted the biopsy you're looking at.
- Nodular hyperplasia of the prostate; AKA benign prostatic hypertrophy (BPH).
- Not diagnosed on needle biopsies.
- BPH is technically incorrect -- the process is a hyperplasia.
- Hyperplasia = proliferation of cells, hypertrophy = enlargement of cells.
- How to remember? A. Prostate... hyperPlasia.
- Hyperplasia = proliferation of cells, hypertrophy = enlargement of cells.
Clinical history
- PSA (serum).
- >10 ng/mL worrisome for prostate cancer.
- Normal is age dependent - increases with age, usu. cut-off ~ 4 ng/mL.
- HIFU = High Intensity Focused Ultrasound - an ablation procedure for prostate cancer.[7]
Specific conditions
Prostatic nodular hyperplasia
- AKA nodular hyperplasia of the prostate.
- AKA benign prostatic hyperplasia (abbreviated BPH).
- AKA benign prostatic hypertrophy.
- This is a misnomer. It is not a hypertrophy.
General
- Very common.
- Incidence increases with age.
Clinical - mnemonic I WISH 2p:[8]
- Intermittency.
- Weak stream.
- Incomplete emptying.
- Straining.
- Hesitancy.
- Post-void dribbling.
- Prolonged voiding.
Treatment:
- Medications.
- Transurethral resection of the prostate (TURP).
Microscopic
Features:
- Stromal and/or glandular hyperplasia.
Note:
- Should not be diagnosed on core biopsy!
Image:
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PROSTATE GLAND, TRANSURETHRAL RESECTION OF THE PROSTATE (TURP): - BENIGN PROSTATIC TISSUE WITH GLANDULAR AND STROMAL PROLIFERATION.
Acute inflammation
General
- A may lead to an increase in the PSA and prompt biopsy.
Microscopic
Features:
- Neutrophils within the glands, between the epithelial cells or within the stroma - key feature.
Note:
- "Prostatitis" is considered a clinical diagnosis.
- Cases are signed-out as "acute inflammation".
- Some pathologists do not comment on the presence (or absence) of inflammation.
- Cases are signed-out as "acute inflammation".
Image:
Chronic inflammation not otherwise specified
General
- Common.
- Non-specific finding.
- Etiology usually not apparent on histomorphology.
Microscopic
Features:
- Lymphocytes within the glands, between the epithelial cells or within the stroma - key feature.
Image:
Sign out
G. PROSTATE, LEFT LATERAL SUPERIOR, BIOPSY: - BENIGN PROSTATE TISSUE; - FOCAL CHRONIC INFLAMMATION.
F. PROSTATE, RIGHT MEDIAL MIDZONE, BIOPSY: - BENIGN PROSTATE TISSUE; - CHRONIC INFLAMMATION.
Note:
- Opinion is divided on whether this finding should be reported.
- Advocates for reporting inflammation say "[i]t is just reporting what you see and may explain the bump in PSA."
- Naysayers opine that "[i]t may provide false assurance that no cancer is present."
Granulomatous prostatitis
General
- Common.
- Usually secondary to BCG treatment of bladder cancer.
- Several classifications exist[9] - the most commonly used is by Epstein & Hutchins.
Epstein & Hutchins classification
The groupings:[10]
- Non-specific.
- No cause identified, usu. incidentally discovered.
- Most common.
- Post-TURP.
- Palisading granuloma with necrotic core (histology similar to a rheumatoid nodule[11][12]) +/- eosinophils.
- Specific.
- Identifiable infectious agent, usu. BCG (in the context of treating bladder cancer), rarely tuberculosis and even more rarely various fungi and syphilis.
- Allergic granulomatous prostatitis.
- Usually associated with eosinophils.
- Examples:
Microscopic
Features:
- Granulomas in the prostate - key feature.
- Palisading granulomas with a necrotic core (similar to a rheumatoid nodule) consistent a prior TURP.[11]
- +/-Eosinophils.
Images:
- Granulomatous inflammation of the prostate/bladder neck - low mag. (WC).
- Granulomatous inflammation of the prostate/bladder neck - high mag. (WC).
Stains
Note:
- Stains are indicated when there is a suspicion of an infective etiology based on histomorphology or clinical information (e.g. immunosuppression).
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PROSTATE GLAND, TRANSURETHRAL RESECTION OF THE PROSTATE (TURP): - BENIGN PROSTATIC TISSUE WITH GLANDULAR AND STROMAL PROLIFERATION. - PALISADING GRANULOMA WITH NECROTIC CORE, SEE COMMENT. COMMENT: This is morphologically consistent with a post-TURP granuloma.
Atrophy of the prostate
General
- Small glands (may mimic Gleason score 3 pattern).
Microscopic
Features:
- Glands often have a jagged edges/prows (in cancer the glands tend to have round edges) - key feature.
- Prow = forward most part of a ship's bow that cuts through the water.[13]
- You may have come across prow in the context of breast cancer, i.e. tubular carcinoma.
- Prow = forward most part of a ship's bow that cuts through the water.[13]
- Gland density is usually lower than in prostate carcinoma, i.e. glands are not back-to-back - key feature.
- Atrophic glands are often hyperchromatic.[14]
- Scant cytoplasm - usually.
Negatives:
- Nuclei like normal, i.e. nucleoli uncommon.
- Should have two cell layers, i.e. epithelial and myoepithelial (may be difficult to see).
Notes:
- Atrophic glands may be scattered with non-atrophic ones.
- IHC may be misleading - basal cell loss.
DDx:
Atrophy versus cancer
Histologic feature | Atrophy | Cancer |
---|---|---|
Glandular architecture/ arrangement |
angulated glands, may look like they originate from one large duct |
round glands, often back-to-back |
Nuclear hyperchromasia |
marked | moderate |
Cytoplasm | scant/minimal | moderate, may be amphophilic |
Basal cells | may be visible | absent |
Nucleoli | absent | present |
Secretions in glands |
no | yes - eosinophilic or blue |
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Generally, this finding is not reported; it is considered a normal finding.
Prostatic infarct
- AKA prostatic infarction.
General
- Rare < 0.1% of core biopsies.[15]
- Can mimic cancer - urothelial carcinoma.[15]
- Prostate usually large.
Microscopic
Features:
- Classic findings of necrosis:
- Karyolysis (loss of nuclei), karyorrhexis (frag. of nuclei), pyknosis (small shrunken nuclei).
- +/-Squamous metaplasia of prostate gland epithelium.
Notes:
- Corpora amylacea - help... call it benign.
- Glands maintain normal spacing.
DDx:
- Urothelial carcinoma with squamous differentiation.
Image:
Basal cell hyperplasia of the prostate
General
- Benign lesion that can be misdiagnosed as cancer.[16]
Microscopic
Features:[17]
- Low power gland architecture near normal.[18][19]
- Glands not as small as cancer.
- Folds in gland lumina.
- No hyperchromasia.
- Two cell populations (as in normal prostate glands).
- May have nucleoli.
DDx:
Image:
High-grade prostatic intraepithelial neoplasia
- Abbreviated as HGPIN.
- May be referred to as prostatic intraepithelial neoplasia, abbreviated PIN.
General
- Thought to be a precursor lesion for prostate adenocarcinoma.
Low-grade prostatic intraepithelial neoplasia:
- Not reported and generally believed to be irrelevant biologically/clinically.
- PIN not otherwise specified refers to HGPIN.
- Low-grade PIN has the architecture of HGPIN but lacks the nuclear atypia.
Microscopic
Features:
- Diagnosed on basis of nuclear changes.
- Hyperchromatic nuclei - key (low power) feature.
- Nucleoli present - key (high power) feature.
- Often increased N/C ratio.
- Nuclear enlargement.
- Different architectures (e.g. micropapillary).
- Usually epithelial hyperplasia.
Notes:
- Nucleoli should be visible with the 20x objective.
- If one uses the 40x objective... one over calls.
- May need IHC for cancer versus HGPIN.
DDx:
- Basal cell hyperplasia of the prostate.
- Intraductal carcinoma of the prostate.
- Prostatic adenocarcinoma - glands with HGPIN have two or more distinct cells layers.
- Benign prostate - HPGIN has nuclear changes.
HGPIN architecture
There are several forms:[22][23]
- Flat - uncommon.
- Tufting - common.
- Micropapillary - common.
- Cribriform - rare.
Note:
- The architectural pattern is NOT thought to have any prognostic significance; however, it may be useful for differentiating it from benign prostate.
Images:
IHC
- HGPIN: AMACR +ve, p63 +ve, HMWCK +ve.
- Cancer: AMACR +ve, p63 -ve, HMWCK -ve.
- Normal: AMACR -ve, p63 +ve, HMWCK +ve.
Atypical small acinar proliferation
- Abbreviated ASAP.
- AKA suspicious for carcinoma.[24]
- ASAP is preferred as it does not contain the word carcinoma and, thus, cannot be misread as carcinoma, i.e. positive for malignancy.
General
- It is a waffle diagnosis, i.e. it is not considered an entity with a distinct pathobiology.[25]
- Analogous to ASCUS on a pap test.
- ASAP should be used sparingly.
- One benchmark is < 3-5% of biopsies.[26]
- Never diagnosed on excision, i.e. prostatectomy specimen.
Association with adenocarcinoma
- On subsequent biopsy - chance of finding adenocarcinoma is approximately 40%; this is higher than if there is high-grade prostatic intraepithelial neoplasia (HGPIN).[27]
Management
- ASAP is considered an indication for re-biopsy;[28] in one survey of urologists[29] 41/42 (~98%) of respondents considered it a sufficient reason to re-biopsy.
Microscopic
Features:
- Atypical appearing acini.
- Limited extent, e.g. 2-3 glands.
Notes:
- IHC not contributory.
- Deeper cuts didn't yield anything - important.
DDx:
Intraductal carcinoma of the prostate
General
- Associated with a poor prognosis.[30]
- Strong association with aggressive invasive carcinomas on prostatectomy when identified in isolation on biopsy.[31]
Microscopic
Features:
- Malignant cells in glands with basal cells - key feature.
- Two cell populations:
- Obviously malignant cells with enlarged nuclei, granular chromatin, hyperchromasia and nucleoli.
- Cells with pale cytoplasm and smaller nuclei.
- Two cell populations:
DDx:
IHC
Features - basal cells present:
- HMWK +ve.
Prostatic adenocarcinoma
General
- Very common.
- Increasing incidence with age - the age in years is an approximation of the percentage of men with prostate cancer.
- Usually an indolent course - most old men die with prostate cancer not from prostate cancer.
Management
The management changes between Gleason 6, 7 & 8; typically, the implications are:
- Gleason 6: watchful waiting or radioactive seeds; surgery if patient wants.
- Gleason 7: do something - often surgery.
- Gleason 8+: bad cancer - do something quickly!
Bottom line:
- You want to be sure when you call something Gleason pattern 4.
Microscopic
Criteria as a list
Major criteria (the ABCs of prostate pathology):[32]
- Architecture.
- Increased gland density.
- Small circular glands.
- In rare subtypes - large branching glands.
- "Infiltrative growth" pattern - malignant glands between benign ones.
- Basal cells lacking.
- Cytological abnormalities:
- Nuclear enlargement.
- Nucleoli.
Minor criteria:[32]
- Nuclear hyperchromasia.
- Wispy blue mucin.
- Image: Wispy blue mucin (nature.com) - from Epstein.[33]
- Pink amorphous secretions.
- Image: Pink amorphous secretions (nature.com) - from Epstein.[33]
- Intraluminal crystalloid.
- Image: Intraluminal crystalloid (nature.com) - from Epstein.[33]
- Amphophilic cytoplasm.
- Amphopilic is said to be bluish-red[34] -- though might also be described as blue-grey.
- Adjacent HGPIN.
- Mitoses - quite rare.
Extent/quantity criteria:
- There is no agreed upon minimum number of glands; however, one paper suggests that agreement among experts is low with 5 or less glands.[35]
- Thus, it has been suggested that six or more glands should be present to diagnose cancer.[35]
Low power features
- Architecture is the key to diagnosing low grade cancer.
- Back-to-back glands or crowding of glands -- think low grade cancer (Gleason pattern 3).
- Sharp transition between gland border and lumen.
- Loss of epithelial folding at the epithelium-gland lumen interface - "punched-out" appearance.
- Eosinophilic debris within the gland lumen (pink amorphous secretions, intraluminal crystalloid).
- Blue-tinged acellular material within the gland lumen (mucin) -- uncommon.
- "Infiltrative": small round/oval (malignant) glands (approx. 5 cells across) interspersed with larger (benign) glands that are 2-3 times larger.
High power features
- Nuclei.
- Hyperchromatic nuclei (like in HGPIN).
- Nuclear enlargement.
- Difficult to appreciate (if cancer isn't side-by-side with normal prostate).
- Difficult to see if not on high power.
- Nucleoli visible on high power (200x or 100X)
- May be difficult to see - especially if light intensity is low.
- One should not use 400x to look for nucleoli (it is a waste of time + you risk overcalling something benign).
- If I see three good nucleoli in a gland I'm usually confident it is cancer.
- May be difficult to see - especially if light intensity is low.
- Loss of basal cells - diagnostic feature.
- Like in breast pathology (where one looks for loss of myoepithelial cells) - this may be difficult to see.
Notes:
- Mitoses are not a common feature - don't waste time looking for them.
Mimics
Mimics of prostate adenocarcinoma:[36]
Entity | Key feature | Detailed microscopic | Other | Image |
---|---|---|---|---|
Adenosis (AKA atypical adenomatous hyperplasia) | gradual transition between normal & small gland (NOT two populations) | many small glands, lack nuclear size variation, basal layer present | nucleoli may be present; may need to do p63 or 34betaE12 to find basal layer | AAH (webpathology.com) |
Sclerosing adenosis | gradual transition between normal & small gland (NOT two populations), fibrosis | many small glands, lack nuclear size variation, basal layer present | analogous to sclerosing adenosis of breast (???) | Sclerosing adenosis (webpathology.com) |
Atrophy | sharp angulation of gland | nuclear hyperchromasia, scant cytoplasm | may appear right beside non-atrophic tissue | Atrophy (webpathology.com), Partial atrophy (webpathology.com) Sclerotic atrophy (webpathology.com) |
Basal cell hyperplasia | two distinct cell populations (in epithelial component) | abundant epithelial cells; nucleoli in pale ('blue') nuclei of basal cells, glandular cell nuclei darker ('purple') | vaguely similar to epithelial hyperplasia of usual type (EHUT) in breast | BCH (webpathology.com) |
Bulbourethral gland | no nuclear atypia | clear cytoplasm | apex of prostate | Cowper gland (webpathology.com) |
Seminal vesicles / ejaculatory ducts | lipofuscin (yellow granular material in cytoplasm), smudge cells (smeared appearance + hyperchromatic) | fern-like arrangement of epithelium (low power), nucleoli, surrounded by muscle, +/- nuclear inclusions | involvement by cancer changes staging, lipofuscin may be present in prostate, often has marked nuc. size var.; location: usu. base of prostate | SV - high mag. (WC), SV - low mag. (WC) |
Radiation effect | marked nuclear size variation | increased stroma (fibrosis), lack nucleoli ??? | history of Rx; uniform nuc. size with Hx of Rx should raise susp. of cancer | Radiation changes (webpathology.com), Radiation changes (webpathology.com) |
Prostatitis | inflammatory cells (lymphocytes, plasma cells, PMNs) | no nuclear atypia, normal gland arch. | clinical mimic of cancer (elevated PSA); usu. not a problem for the pathologist | Prostatic inflammation (WC) |
Vasitis nodosa | sperm within ducts, clinical history (usu. post-vasectomy) | small tubules, nucleoli common, mild atypia, may "invade" vessels, track along nerves | mimics metastatic prostate carcinoma, IHC stains: PSA-, PSAP- | VN (webpathology.com) |
Memory device: AAABBRS = atrophy, adenosis, adenosis (sclerosing), basal cell hyperplasia, bulbourethral gland, radiation, seminal vesicles.
Gleason grading system
Overview:
- This system is only one any one talks about.
- Score range: 6-10.
- Technically 2-10... but almost no one uses 2-5.
- Reported as on biopsy as: (primary pattern) + (secondary pattern or tertiary pattern with the highest grade) = sum.
- e.g. Gleason score 3+4=7 means: pattern 3 is present and dominant, pattern 4 is the remainder of the tumour - but present in a lesser amount than pattern 3.
- Reported as on prostatectomies as: (primary pattern) + (secondary pattern) = sum, (tertiary pattern)
- Tertiary Gleason pattern - definition: a pattern that is seen in than 5% of the tumour (volume), that is higher grade than the two dominant patterns.[37]
- The presence of a tertiary patterns adversely affect the prognosis; however, the prognosis is not as bad as when the tertiary pattern is the secondary pattern, i.e. 3+4 tertiary 5 has a better prognosis than 3+5 (with some small amount of pattern 4).[37]
Examples:
- A biopsy has 80% pattern 4, 16% pattern 3 and 4% pattern 5... it would be reported as: 4+5=9.
- A prostatectomy has 80% pattern 4, 16% pattern 3 and 4% pattern 5... it would be reported as: 4+3=7 with tertiary pattern 5.
Testing yourself:
- There is a nice test-yourself quiz from Johns Hopkins: http://162.129.103.34/prostate/.
- It was studied in a paper by Kronz et al.[38]
Gleason pattern 1 & 2
- Use strongly discouraged by a number of GU pathology experts.
Notes:
- Gleason pattern 1 - probably represents what today would be called adenosis.
- Should never be used.
- Gleason pattern 2 - used by few GU pathology experts occasionally.
- Generally, should not be diagnosed on core biopsies.[39]
Gleason pattern 3
- Glands smaller than normal prostate glands + loss of epithelial folding.
- Can draw a line around each gland.
- May have gland branching.
- Glands have a X, U, V or Y shape.
Notes:
- Gland lumina should be seen.
- All cribriform is now, generally, classified as Gleason pattern 4.[39]
Gleason pattern 4
- Loss of gland lumina.
- Gland fusion.
- Benign looking cords ('hypernephroid pattern').
- Cribriform.
- Glomeruloid pattern - resembles a glomerulus.
Notes:
- One gland is not enough to call Gleason 4.
Images:
- Gleason pattern 4 - cribriform (WC).
- Gleason pattern 4 - small glands & Gleason pattern 5 - single cells (WC).
- Glomeruloid pattern (nature.com).
Gleason pattern 5
- Sheets.
- Must be differentiated from intraductal growth (which like in the breast are well circumscribed nests).
- Single cells.
- May be confused with stromal/lymphocytic infiltration.
- Look for nucleoli, cells should be round (prostatic stroma cells are spindle cells).
- May be confused with stromal/lymphocytic infiltration.
- Cords.
- Nests of cells with necrosis at centre.
Image: Gleason pattern 4 - small glands & Gleason pattern 5 - single cells (WC).
Special types
Special types of prostate cancer have set Gleason scores:[40]
Special type | Gleason pattern | Comment |
---|---|---|
Ductal carcinoma | 4 | may be graded 3 or 5[41] |
Mucinous carcinoma | 4 | |
Sarcomatoid carcinoma | 5 | glands graded separately |
Signet ring cell carcinoma | 5 | |
Small cell carcinoma | not graded | may be graded 5[41] |
Adenosquamous and squamous carcinoma | not graded | |
Lymphoepithelioma-like carcinoma | not graded | |
Adenoid cystic carcinoma | not graded | |
Urothelial carcinoma | not graded | |
Undifferentiated carcinoma, NOS | not graded |
How to remember the ones that aren't graded - think of Ur Lung carcinomas (Urothelial carcinoma, Lymphoepithelioma-like carcinoma):
- Small cell carcinoma.
- Squamous cell carcinoma.
- Adenosquamous carcinoma.
- Adenoid cystic carcinoma.
Staging parameters and margins
Surgical margins
- Positive is tumour touching ink.[42]
- "Close" margins have an increase recurrence risk.
Notes:
- Surgical margin - where the surgeon cut.
- It is possible to have EPE without a positive margin.
- It is possible to have a positive margin without EPE.
Rates and implication
Positivity rate varies substantially (13-44%):
- Norway: 26% -- strong dependence on surgeon volume (18% high case load vs. 44% low case load).[43]
- France: 13-17%.[44]
Note:
- There is likely a strong dependence on stage and grade of cancer, i.e. surgeons that operate more on high grade cancers will probably have a higher margin positive rates.
The impact of positive margins:
- Significant modest negative affect on long-term outcome in node negative cancers (pT2-4 pN0).[45]
- Weaker impact than stage and Gleason score.[46]
Extraprostatic extension
- Abbreviated EPE.
General:
- Extraprostatic extension (EPE) is difficult to assess (in prostatectomy specimens) as there is no consensus definition.
- The prostate does NOT have a well defined capsule.
- Intraobserver agreement for EPE is fair-moderate and lower than for the surgical margin.[47]
- The prostate does NOT have a well defined capsule.
- EPE, typically, upstages tumours from T2x to T3a.
Prostatectomy specimens - EPE is present if there is either:
- A "significant bulge" in the contour of the prostate at low power and no fibromuscular tissue surrounding the malignant cells.
- Malignant cells directly adjacent to peri-prostatic adipose tissue.
Note:
- The prostate, at the apex, may have some skeletal muscle. Thus, it is difficult to define extention... ergo EPE not called at the apex.
Prostate biopsy - EPE is present if:
Seminal vesicle invasion
- Tumour must be in the muscle surrounding the epithelial component - the connective tissue surrounding the seminal vesicle does not count.[50]
IHC
- AMACR +ve.
- AR +ve -- in prostate confined cancer.
- Usu. -ve in LN +ve disease.[51]
- PSA +ve.
- PSAP +ve.
- May be positive in hindgut neuroendocrine tumours.[52]
- p63 -ve.
- HMWCK (34betaE12) -ve.
Combination immunostains:
Molecular changes in prostate cancer
A fusion gene between TMPRSS2 and ERG is described.[56][57]
- Both genes are on chromosome 21.
- Currently not used diagnostically.
- Fusion gene seen in approximately 50% of prostate cancer.[57]
- A subset of TMPRSS2-ERG known as 2+Edel (seen in ~7% of all prostate cancer cases) predicts poor survival.[58]
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Prostatectomy specimens
See: CAP checklist.
Biopsy specimens
Important elements - a list:[32]
- Type of cancer, e.g. "prostatic adenocarcinoma, acinar type".
- Gleason score including primary and secondary pattern, e.g. "Gleason score 3+4=7".
- Number of cores and number involved, e.g. "2/3 cores involved by cancer".
- Percent area involved, i.e. how much of the core is cancer, e.g. "75% of specimen is tumour".
- Percent area involved that is Gleason pattern 4 or 5, e.g. "25% of the tumour is Gleason pattern 4 or 5".
- Presence of perineural invasion.
- Presence of extension into fat (extraprostatic extension).
Notes:
- "Percent area involved" may seem like an odd thing to request 'cause it is sampling dependent, i.e. if the radiologist sticks the biopsy needle deeper into the lesion more of the core is positive, but urologists think it is important -- more important than perineural invasion.[59]
Completely negative
A. PROSTATE, RIGHT LATERAL SUPERIOR, BIOPSY: - BENIGN PROSTATE TISSUE. B. PROSTATE, RIGHT MEDIAL SUPERIOR, BIOPSY: - BENIGN PROSTATE TISSUE. C. PROSTATE, RIGHT LATERAL MIDZONE, BIOPSY: - BENIGN PROSTATE TISSUE. D. PROSTATE, RIGHT MEDIAL MIDZONE, BIOPSY: - BENIGN PROSTATE TISSUE. E. PROSTATE, RIGHT LATERAL INTERIOR, BIOPSY: - BENIGN PROSTATE TISSUE. F. PROSTATE, RIGHT MEDIAL INFERIOR, BIOPSY: - BENIGN PROSTATE TISSUE. G. PROSTATE, LEFT LATERAL SUPERIOR, BIOPSY: - BENIGN PROSTATE TISSUE. H. PROSTATE, LEFT MEDIAL SUPERIOR, BIOPSY: - BENIGN PROSTATE TISSUE. I. PROSTATE, LEFT LATERAL MIDZONE, BIOPSY: - BENIGN PROSTATE TISSUE. J. PROSTATE, LEFT MEDIAL MIDZONE, BIOPSY: - BENIGN PROSTATE TISSUE. K. PROSTATE, LEFT LATERAL INTERIOR, BIOPSY: - BENIGN PROSTATE TISSUE. L. PROSTATE, LEFT MEDIAL INFERIOR, BIOPSY: - BENIGN PROSTATE TISSUE.
No glands
F. PROSTATE, RIGHT MEDIAL MIDZONE, BIOPSY: - BENIGN FIBROMUSCULAR TISSUE; - NO PROSTATIC GLANDULAR TISSUE PRESENT.
Inflammation
G. PROSTATE, LEFT LATERAL SUPERIOR, BIOPSY: - BENIGN PROSTATE TISSUE; - FOCAL CHRONIC INFLAMMATION.
F. PROSTATE, RIGHT MEDIAL MIDZONE, BIOPSY: - BENIGN PROSTATE TISSUE; - CHRONIC INFLAMMATION.
F. PROSTATE, RIGHT MEDIAL MIDZONE, BIOPSY: - BENIGN PROSTATE TISSUE; - ACUTE AND CHRONIC INFLAMMATION.
Positive
F. PROSTATE, RIGHT MEDIAL INFERIOR, BIOPSY: - ADENOCARCINOMA, GLEASON SCORE 6/10 (3+3); - 1/1 CORE INVOLVED; APPROXIMATELY 5% OF TISSUE INVOLVED.
F. PROSTATE, RIGHT MEDIAL INFERIOR, BIOPSY: - ADENOCARCINOMA, GLEASON SCORE 6/10 (3+3); - 1/1 CORE INVOLVED; APPROXIMATELY 25% OF TISSUE INVOLVED; - PERINEURAL INVASION PRESENT.
G. PROSTATE, LEFT LATERAL SUPERIOR, BIOPSY: - ADENOCARCINOMA, GLEASON SCORE 7/10 (4+3); - 1/1 CORE INVOLVED; APPROXIMATELY 5% OF TISSUE INVOLVED; - PERINEURAL INVASION PRESENT.
H. PROSTATE, LEFT MEDIAL SUPERIOR, BIOPSY: - ADENOCARCINOMA, GLEASON SCORE 8/10 (4+4); - 1/1 CORE INVOLVED; APPROXIMATELY 15% OF TISSUE INVOLVED.
H. PROSTATE, LEFT MEDIAL SUPERIOR, BIOPSY: - ADENOCARCINOMA, GLEASON SCORE 8/10 (4+4); - 1/1 CORE INVOLVED; APPROXIMATELY 15% OF TISSUE INVOLVED; - PERINEURAL INVASION PRESENT.
TUMOUR SUMMARY - PROSTATE CORE BIOPSIES: - HISTOLOGIC TYPE: ADENOCARCINOMA (ACINAR, NOT OTHERWISE SPECIFIED). - TOTAL GLEASON SCORE: 7. - PRIMARY PATTERN: 4. - SECONDARY PATTERN: 3. - PERCENT OF TUMOUR WITH PATTERN HIGHER THAN GRADE 3: 75%. - NUMBER OF CORES POSITIVE: 10. - TOTAL NUMBER OF CORES: 12. - TOTAL LINEAR MILLIMETERS OF NEEDLE CORE TISSUE: 152 MM. - PERCENT OF NEEDLE CORE TISSUE THAT IS TUMOUR: 44%. - PERIPROSTATIC FAT INVASION: NOT IDENTIFIED. - SEMINAL VESICLE INVASION: SEMINAL VESICLE NOT IDENTIFIED. - LYMPHOVASCULAR INVASION: NOT IDENTIFIED. - PERINEURAL INVASION: PRESENT. - ADDITIONAL FINDINGS: HIGH-GRADE PROSTATIC INTRAEPITHELIAL NEOPLASIA, CHRONIC INFLAMMATION (FOCAL).
Unusual forms of prostate cancer
Prostatic ductal adenocarcinoma
General
- Sometimes it is referred to as endometrioid or endometrial adenocarcinoma; both terms are discouraged.[60]
- Controversial - may represent acinar adenocarcinoma with periurethral ducts involvement.[61]
Microscopic
Features:[62]
- Pseudostratified (crowded appearing) columnar (or cigar-shaped) nuclei - key feature.
- Vaguely resembles colonic adenocarcinoma.
- Variable architecture:
- Papillary.
- Cribriform.
- Single gland (large glands).
- Endometrioid - vaguely looks like endometrial carcinoma (with back-to-back glands).
Notes:
- Usually seen in association with conventional (acinar) prostate adenocarcinoma.
Images:
- Prostatic ductal adenocarcinoma - several images (upmc.edu).
- Prostatic ductal adenocarcinoma - another case - several images (upmc.edu).
- Prostatic ductal adenocarcinoma - F1 (nih.gov).
- Prostatic ductal adenocarcinoma - F2 (nih.gov).
- Prostatic ductal adenocarcinoma (webpathology.com).
IHC
Features:[63]
- p53 +ve in ~ 75% of cases.
- Ki-67 high in ~ 70% of cases.
- Chromogranin A +ve (cytoplasm) in ~ 70% of cases.
Others:[64]
- PSA +ve.
PIN-like prostatic ductal adenocarcinoma
General
- Recently described.[65][66]
- May be confused with prostatic intraepithelial neoplasia (PIN).
Microscopic
Features:[65]
- Stratified malignant epithelium.
Note:
- Vaguely similar to a tubular adenoma of the colon.
DDx:
Image:
Foamy gland carcinoma
General
- Rare.
Microscopic
Features:
- Tufted glandular border.
- Abundant eosinophilic (or hyperchromatic) cytoplasm - key feature.
- Gland size larger than "typical" prostate cancer.
Image: Foamy gland carcinoma (nature.com).
Atrophic prostate carcinoma
- AKA atrophic carcinoma.
General
- Uncommon.
Note:
- An atrophic component in prostate cancer is common; one study identified it in ~15% of cases.[67]
Microscopic
Features:
- Scant cytoplasm.
- Nuclear features of conventional prostate cancer (nucleoli, nuclear enlargement).
- Increased gland density.
DDx:
Image: Atrophic carcinoma (nature.com).
Mucinous prostate carcinoma
General
- Rare.
Microscopic
Features:
- Cytologically malignant cells floating in mucin.
- > 25% of tumour mucinous.[40]
- One study suggests >= 25%.[68]
DDx:
- Metastatic mucinous carcinoma.
Notes:
- Mucinous carcinoma - percentage required to call varies by site.
Pseudohyperplastic prostatic adenocarcinoma
General
- Rare.
Microscopic
- Medium to large glands with an atypical morphology - key low power feature:
- Papillary or pseudopapillary infoldings, luminal undulations, branching or cystic dilatation.
- Nuclear features of conventional prostate cancer (nucleoli, nuclear enlargement).
Image: Pseudohyperplastic prostatic adenocarcinoma (nature.com).
Notes:
- Usually associated with conventional (acinar) prostate adenocarcinoma.
- Pale abundant cytoplasm - similar to normal prostate.
Prostatic signet ring cell carcinoma
General
- Very rare - 9 cases in a series of 29,783 prostate cancer cases.[71]
- Criteria vary - percentage of SRCs required for Dx varies from 20% to 50%.[71]
Microscopic
Features:
- Signet ring cells - see basics article.
Image:
Sarcomatoid prostate carcinoma
- AKA carcinosarcoma.
General
- Rare.
Microscopic
Features:[72]
- Biphasic tumour:
- Spindle cells (sarcomatous component).
- May include components of: osteosarcoma, chondrosarcoma and/or rhabdomyosarcoma.
- Glandular component (like conventional prostate carcinoma).
- Spindle cells (sarcomatous component).
IHC
Features - typical:[72]
- PSA +ve.
- Keratin +ve.
Small cell carcinoma of the prostate gland
General
- Rare.
Microscopic
Features:
- Nuclear moulding.
- Stippled chromatin.
- High NC ratio.
- Small cells.
Notes:
- Similar to small cell carcinoma of the lung.
- High-grade squamoid component favours metastatic urothelial carcinoma.
- UCC usu. HWCK +ve.
Adenoid cystic/basal cell carcinoma of the prostate
- Abbreviated ACBCC.
General
- Rare.
- Typically indolent - may be aggressive.[73]
Microscopic
Features:
- Adenoid cystic carcinoma-like and basal cell adenoma-like:
- Nests of cells that have round spaces filled by whispy blue mucin.
- Dense collagenous stroma.
Images:
IHC
- HER2/neu +ve (strong).[74]
See also
References
- ↑ McNeal, JE. (Aug 1988). "Normal histology of the prostate.". Am J Surg Pathol 12 (8): 619-33. PMID 2456702.
- ↑ Christian JD, Lamm TC, Morrow JF, Bostwick DG (January 2005). "Corpora amylacea in adenocarcinoma of the prostate: incidence and histology within needle core biopsies". Mod. Pathol. 18 (1): 36–9. doi:10.1038/modpathol.3800250.
- ↑ Trpkov, K.; Bartczak-McKay, J.; Yilmaz, A. (Aug 2009). "Usefulness of cytokeratin 5/6 and AMACR applied as double sequential immunostains for diagnostic assessment of problematic prostate specimens.". Am J Clin Pathol 132 (2): 211-20; quiz 307. doi:10.1309/AJCPGFJP83IXZEUR. PMID 19605815.
- ↑ PR. September 2009.
- ↑ Leroy X, Ballereau C, Villers A, et al. (April 2003). "MUC6 is a marker of seminal vesicle-ejaculatory duct epithelium and is useful for the differential diagnosis with prostate adenocarcinoma". Am. J. Surg. Pathol. 27 (4): 519–21. PMID 12657938.
- ↑ URL: http://www.cancer.gov/dictionary?cdrid=446218. Accessed on: 23 February 2012.
- ↑ URL: http://www.internationalhifu.com/what-is-hifu-mainmenu-132.html. Accessed on: 15 June 2010.
- ↑ TN06 U5
- ↑ Uzoh, CC.; Uff, JS.; Okeke, AA. (Mar 2007). "Granulomatous prostatitis.". BJU Int 99 (3): 510-2. doi:10.1111/j.1464-410X.2006.06585.x. PMID 17092284.
- ↑ Epstein, JI.; Hutchins, GM. (Sep 1984). "Granulomatous prostatitis: distinction among allergic, nonspecific, and post-transurethral resection lesions.". Hum Pathol 15 (9): 818-25. PMID 6432674.
- ↑ 11.0 11.1 Mies, C.; Balogh, K.; Stadecker, M. (Mar 1984). "Palisading prostate granulomas following surgery.". Am J Surg Pathol 8 (3): 217-21. PMID 6703198.
- ↑ URL: http://www.humpath.com/spip.php?article18010. Accessed on: 26 September 2012.
- ↑ http://en.wikipedia.org/wiki/Prow
- ↑ SN. June 3, 2009.
- ↑ 15.0 15.1 Milord, RA.; Kahane, H.; Epstein, JI. (Oct 2000). "Infarct of the prostate gland: experience on needle biopsy specimens.". Am J Surg Pathol 24 (10): 1378-84. PMID 11023099.
- ↑ Cleary, KR.; Choi, HY.; Ayala, AG. (Dec 1983). "Basal cell hyperplasia of the prostate.". Am J Clin Pathol 80 (6): 850-4. PMID 6195916.
- ↑ URL: http://pathologyoutlines.com/prostate.html#bch. Accessed on: 28 June 2010.
- ↑ URL: http://www.nature.com/modpathol/journal/v16/n6/fig_tab/3880810f1.html. Accessed on: 28 June 2010.
- ↑ URL: http://www.nature.com/modpathol/journal/v16/n6/fig_tab/3880810f2.html. Accessed on: 28 June 2010.
- ↑ Srigley, JR.; Merrimen, JL.; Jones, G.; Jamal, M. (Dec 2010). "Multifocal high-grade prostatic intraepithelial neoplasia is still a significant risk factor for adenocarcinoma.". Can Urol Assoc J 4 (6): 434. PMID 21191509.
- ↑ Herawi, M.; Kahane, H.; Cavallo, C.; Epstein, JI. (Jan 2006). "Risk of prostate cancer on first re-biopsy within 1 year following a diagnosis of high grade prostatic intraepithelial neoplasia is related to the number of cores sampled.". J Urol 175 (1): 121-4. doi:10.1016/S0022-5347(05)00064-9. PMID 16406886.
- ↑ Humphrey, Peter A; Dehner, Louis P; Pfeifer, John D (2008). The Washington Manual of Surgical Pathology (1st ed.). Lippincott Williams & Wilkins. pp. 380. ISBN 978-0781765275.
- ↑ Bostwick, DG.; Qian, J. (Mar 2004). "High-grade prostatic intraepithelial neoplasia.". Mod Pathol 17 (3): 360-79. doi:10.1038/modpathol.3800053. PMID 14739906. http://www.nature.com/modpathol/journal/v17/n3/pdf/3800053a.pdf.
- ↑ THvdK. 19 June 2010.
- ↑ Flury SC, Galgano MT, Mills SE, Smolkin ME, Theodorescu D (January 2007). "Atypical small acinar proliferation: biopsy artefact or distinct pathological entity". BJU International 99 (4): 780-5. PMID 17378841. http://www3.interscience.wiley.com/journal/118508438/abstract.
- ↑ THvdK. 19 June 2010.
- ↑ Leite KR, Camara-Lopes LH, Cury J, Dall'oglio MF, Sañudo A, Srougi M (June 2008). "Prostate cancer detection at rebiopsy after an initial benign diagnosis: results using sextant extended prostate biopsy". Clinics 63 (3): 339–42. PMID 18568243. http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1807-59322008000300009&lng=en&nrm=iso&tlng=en.
- ↑ Bostwick DG, Meiers I (July 2006). "Atypical small acinar proliferation in the prostate: clinical significance in 2006". Arch. Pathol. Lab. Med. 130 (7): 952–7. PMID 16831049. http://journals.allenpress.com/jrnlserv/?request=get-abstract&issn=0003-9985&volume=130&page=952.
- ↑ Rubin MA, Bismar TA, Curtis S, Montie JE (July 2004). "Prostate needle biopsy reporting: how are the surgical members of the Society of Urologic Oncology using pathology reports to guide treatment of prostate cancer patients?". Am. J. Surg. Pathol. 28 (7): 946–52. PMID 15223967.
- ↑ Henry, PC.; Evans, AJ. (Jul 2009). "Intraductal carcinoma of the prostate: a distinct histopathological entity with important prognostic implications.". J Clin Pathol 62 (7): 579-83. doi:10.1136/jcp.2009.065003. PMID 19246509.
- ↑ Robinson, BD.; Epstein, JI. (Oct 2010). "Intraductal carcinoma of the prostate without invasive carcinoma on needle biopsy: emphasis on radical prostatectomy findings.". J Urol 184 (4): 1328-33. doi:10.1016/j.juro.2010.06.017. PMID 20723921.
- ↑ 32.0 32.1 32.2 Humphrey PA (January 2007). "Diagnosis of adenocarcinoma in prostate needle biopsy tissue". J. Clin. Pathol. 60 (1): 35–42. doi:10.1136/jcp.2005.036442. PMC 1860598. PMID 17213347. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1860598/?tool=pubmed.
- ↑ 33.0 33.1 33.2 Epstein JI (March 2004). "Diagnosis and reporting of limited adenocarcinoma of the prostate on needle biopsy". Mod. Pathol. 17 (3): 307–15. doi:10.1038/modpathol.3800050. PMID 14739905. http://www.nature.com/modpathol/journal/v17/n3/full/3800050a.html.
- ↑ URL: http://pancreaticcancer2000.com/page1.htm. Accessed on: 3 June 2010.
- ↑ 35.0 35.1 Van der Kwast, TH.; Evans, A.; Lockwood, G.; Tkachuk, D.; Bostwick, DG.; Epstein, JI.; Humphrey, PA.; Montironi, R. et al. (Feb 2010). "Variability in diagnostic opinion among pathologists for single small atypical foci in prostate biopsies.". Am J Surg Pathol 34 (2): 169-77. doi:10.1097/PAS.0b013e3181c7997b. PMID 20061936.
- ↑ Weedman Molavi, Diana (2008). The Practice of Surgical Pathology: A Beginner's Guide to the Diagnostic Process (1st ed.). Springer. pp. 100-3. ISBN 978-0387744858.
- ↑ 37.0 37.1 Zhou, Ming; Magi-Galluzzi, Cristina (2006). Genitourinary Pathology: A Volume in Foundations in Diagnostic Pathology Series (1st ed.). Churchill Livingstone. pp. 72. ISBN 978-0443066771.
- ↑ Kronz, JD.; Silberman, MA.; Allsbrook, WC.; Bastacky, SI.; Burks, RT.; Cina, SJ.; Mills, SE.; Ross, JS. et al. (Sep 2000). "Pathology residents' use of a Web-based tutorial to improve Gleason grading of prostate carcinoma on needle biopsies.". Hum Pathol 31 (9): 1044-50. doi:10.1053/hupa.2000.16278. PMID 11014569.
- ↑ 39.0 39.1 Epstein, JI. (Feb 2010). "An update of the Gleason grading system.". J Urol 183 (2): 433-40. doi:10.1016/j.juro.2009.10.046. PMID 20006878. Cite error: Invalid
<ref>
tag; name "pmid20006878" defined multiple times with different content - ↑ 40.0 40.1 Grignon DJ (March 2004). "Unusual subtypes of prostate cancer". Mod. Pathol. 17 (3): 316–27. doi:10.1038/modpathol.3800052. PMID 14976541.
- ↑ 41.0 41.1 URL: https://www.bostwicklaboratories.com/global/physicians/medical-library/articles/gleason-grading.aspx. Accessed on: 26 November 2011.
- ↑ Lu, J.; Wirth, GJ.; Wu, S.; Chen, J.; Dahl, DM.; Olumi, AF.; Young, RH.; McDougal, WS. et al. (Jul 2012). "A close surgical margin after radical prostatectomy is an independent predictor of recurrence.". J Urol 188 (1): 91-7. doi:10.1016/j.juro.2012.02.2565. PMID 22578729.
- ↑ Steinsvik, EA.; Axcrona, K.; Angelsen, A.; Beisland, C.; Dahl, A.; Eri, LM.; Haug, ES.; Svindland, A. et al. (Aug 2012). "Does a surgeon's annual radical prostatectomy volume predict the risk of positive surgical margins and urinary incontinence at one-year follow-up? - Findings from a prospective national study.". Scand J Urol Nephrol. doi:10.3109/00365599.2012.707684. PMID 22860630.
- ↑ Koutlidis, N.; Mourey, E.; Champigneulle, J.; Mangin, P.; Cormier, L. (Jul 2012). "Robot-assisted or pure laparoscopic nerve-sparing radical prostatectomy: What is the optimal procedure for the surgical margins? A single center experience.". Int J Urol. doi:10.1111/j.1442-2042.2012.03102.x. PMID 22860572.
- ↑ Mauermann, J.; Fradet, V.; Lacombe, L.; Dujardin, T.; Tiguert, R.; Tetu, B.; Fradet, Y. (Aug 2012). "The Impact of Solitary and Multiple Positive Surgical Margins on Hard Clinical End Points in 1712 Adjuvant Treatment-Naive pT2-4 N0 Radical Prostatectomy Patients.". Eur Urol. doi:10.1016/j.eururo.2012.08.002. PMID 22901983.
- ↑ Chalfin, HJ.; Dinizo, M.; Trock, BJ.; Feng, Z.; Partin, AW.; Walsh, PC.; Humphreys, E.; Han, M. (Jul 2012). "Impact of surgical margin status on prostate-cancer-specific mortality.". BJU Int. doi:10.1111/j.1464-410X.2012.11371.x. PMID 22788795.
- ↑ Evans, AJ.; Henry, PC.; Van der Kwast, TH.; Tkachuk, DC.; Watson, K.; Lockwood, GA.; Fleshner, NE.; Cheung, C. et al. (Oct 2008). "Interobserver variability between expert urologic pathologists for extraprostatic extension and surgical margin status in radical prostatectomy specimens.". Am J Surg Pathol 32 (10): 1503-12. doi:10.1097/PAS.0b013e31817fb3a0. PMID 18708939.
- ↑ Epstein, JI.; Srigley, J.; Grignon, D.; Humphrey, P. (Sep 2007). "Recommendations for the reporting of prostate carcinoma.". Hum Pathol 38 (9): 1305-9. doi:10.1016/j.humpath.2007.05.015. PMID 17707261.
- ↑ Evans, A. 4 June 2010.
- ↑ Lester, Susan Carole (2010). Manual of Surgical Pathology (3rd ed.). Saunders. pp. 409. ISBN 978-0-323-06516-0.
- ↑ Fleischmann, A.; Rocha, C.; Schobinger, S.; Seiler, R.; Wiese, B.; Thalmann, GN. (Apr 2011). "Androgen receptors are differentially expressed in Gleason patterns of prostate cancer and down-regulated in matched lymph node metastases.". Prostate 71 (5): 453-60. doi:10.1002/pros.21259. PMID 20878946.
- ↑ Azumi, N.; Traweek, ST.; Battifora, H. (Aug 1991). "Prostatic acid phosphatase in carcinoid tumors. Immunohistochemical and immunoblot studies.". Am J Surg Pathol 15 (8): 785-90. PMID 1712549.
- ↑ URL: http://biocare.net/wp-content/uploads/225DS.pdf. Accessed on: 18 October 2011.
- ↑ URL: http://www.antibodies-online.com/antibody/308235/anti-PIN-4+p63+Cytokeratin+HMW+p504S++AMACR/. Accessed on: 18 October 2011.
- ↑ URL: http://www.webpathology.com/image.asp?case=96&n=5. Accessed on: 18 October 2011.
- ↑ Yu J, Yu J, Mani RS, Cao Q, Brenner CJ, Cao X, Wang X, Wu L, Li J, Hu M, Gong Y, Cheng H, Laxman B, Vellaichamy A, Shankar S, Li Y, Dhanasekaran SM, Morey R, Barrette T, Lonigro RJ, Tomlins SA, Varambally S, Qin ZS, Chinnaiyan AM (May 2010). "An Integrated Network of Androgen Receptor, Polycomb, and TMPRSS2-ERG Gene Fusions in Prostate Cancer Progression". Cancer Cell 17 (5): 443–54. doi:10.1016/j.ccr.2010.03.018. PMC 2874722. PMID 20478527. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2874722/.
- ↑ 57.0 57.1 Online 'Mendelian Inheritance in Man' (OMIM) 602060
- ↑ Attard, G.; Clark, J.; Ambroisine, L.; Fisher, G.; Kovacs, G.; Flohr, P.; Berney, D.; Foster, CS. et al. (Jan 2008). "Duplication of the fusion of TMPRSS2 to ERG sequences identifies fatal human prostate cancer.". Oncogene 27 (3): 253-63. doi:10.1038/sj.onc.1210640. PMID 17637754.
- ↑ Rubin MA, Bismar TA, Curtis S, Montie JE (July 2004). "Prostate needle biopsy reporting: how are the surgical members of the Society of Urologic Oncology using pathology reports to guide treatment of prostate cancer patients?". Am. J. Surg. Pathol. 28 (7): 946–52. PMID 15223967.
- ↑ Samaratunga, H.; Delahunt, B. (Aug 2008). "Ductal adenocarcinoma of the prostate: current opinion and controversies.". Anal Quant Cytol Histol 30 (4): 237-46. PMID 18773743.
- ↑ Bock, BJ.; Bostwick, DG. (Jul 1999). "Does prostatic ductal adenocarcinoma exist?". Am J Surg Pathol 23 (7): 781-5. PMID 10403300.
- ↑ Zhou, Ming; Magi-Galluzzi, Cristina (2006). Genitourinary Pathology: A Volume in Foundations in Diagnostic Pathology Series (1st ed.). Churchill Livingstone. pp. 88. ISBN 978-0443066771.
- ↑ Tarján, M.; Lenngren, A.; Hellberg, D.; Tot, T. (Jun 2012). "Immunohistochemical verification of ductal differentiation in prostate cancer.". APMIS 120 (6): 510-8. doi:10.1111/j.1600-0463.2011.02862.x. PMID 22583364.
- ↑ Kumar, A.; Mukherjee, SD. (Apr 2010). "Metastatic ductal carcinoma of the prostate: a rare variant responding to a common treatment.". Can Urol Assoc J 4 (2): E50-4. PMID 20368883.
- ↑ 65.0 65.1 Hameed, O.; Humphrey, PA. (Jul 2006). "Stratified epithelium in prostatic adenocarcinoma: a mimic of high-grade prostatic intraepithelial neoplasia.". Mod Pathol 19 (7): 899-906. doi:10.1038/modpathol.3800601. PMID 16607376.
- ↑ Lee, TK.; Miller, JS.; Epstein, JI. (Jun 2010). "Rare histological patterns of prostatic ductal adenocarcinoma.". Pathology 42 (4): 319-24. doi:10.3109/00313021003767314. PMID 20438402.
- ↑ Kaleem, Z.; Swanson, PE.; Vollmer, RT.; Humphrey, PA. (Jun 1998). "Prostatic adenocarcinoma with atrophic features: a study of 202 consecutive completely embedded radical prostatectomy specimens.". Am J Clin Pathol 109 (6): 695-703. PMID 9620026.
- ↑ Osunkoya AO, Nielsen ME, Epstein JI (March 2008). "Prognosis of mucinous adenocarcinoma of the prostate treated by radical prostatectomy: a study of 47 cases". Am. J. Surg. Pathol. 32 (3): 468–72. doi:10.1097/PAS.0b013e3181589f72. PMID 18300802.
- ↑ Zhou, Ming; Magi-Galluzzi, Cristina (2006). Genitourinary Pathology: A Volume in Foundations in Diagnostic Pathology Series (1st ed.). Churchill Livingstone. pp. 77. ISBN 978-0443066771.
- ↑ Arista-Nasr J, Martinez-Benitez B, Valdes S, Hernández M, Bornstein-Quevedo L (2003). "Pseudohyperplastic prostatic adenocarcinoma in transurethral resections of the prostate". Pathol. Oncol. Res. 9 (4): 232–5. doi:PAOR.2003.9.4.0232. PMID 14688829.
- ↑ 71.0 71.1 Warner, JN.; Nakamura, LY.; Pacelli, A.; Humphreys, MR.; Castle, EP. (Dec 2010). "Primary signet ring cell carcinoma of the prostate.". Mayo Clin Proc 85 (12): 1130-6. doi:10.4065/mcp.2010.0463. PMID 21123640.
- ↑ 72.0 72.1 Zhou, Ming; Magi-Galluzzi, Cristina (2006). Genitourinary Pathology: A Volume in Foundations in Diagnostic Pathology Series (1st ed.). Churchill Livingstone. pp. 77 & 80. ISBN 978-0443066771.
- ↑ Iczkowski, KA.; Ferguson, KL.; Grier, DD.; Hossain, D.; Banerjee, SS.; McNeal, JE.; Bostwick, DG. (Dec 2003). "Adenoid cystic/basal cell carcinoma of the prostate: clinicopathologic findings in 19 cases.". Am J Surg Pathol 27 (12): 1523-9. PMID 14657711.
- ↑ Iczkowski, KA.; Montironi, R. (Dec 2006). "Adenoid cystic/basal cell carcinoma of the prostate strongly expresses HER-2/neu.". J Clin Pathol 59 (12): 1327-30. doi:10.1136/jcp.2005.035147. PMID 17142577.
External links
- CAP prostate check list - cap.org.
- CAP prostate protocol - cap.org.
- Gleason score quiz - Johns Hopkins Prostate Center.