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GU BreakOut Session

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Title: GU BreakOut Session


1
GU Break-Out Session
  • L. Priya Kunju, M.D.
  • Assistant Professor
  • Department of Pathology
  • The University of Michigan

2
Case 1
  • 62 Y, PSA 8.1
  • Underwent prostate NBX

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Case 1
  • Diagnosis
  • Prostate carcinoma, pseudohyperplastic variant,
    Gleason Score 336

5
Pseudohyperplastic Prostate Carcinoma
  • Recently recognized entity
  • Resembles architecturally benign hyperplastic
    prostate glands and/or HGPIN
  • Incidence NBX 2, Rad Prostatectomy 11
  • Cytologic atypia always present


  • (Humphery et al, AJSP,1998)

6
Pseudohyperplastic CarcinomaDiagnostic Criteria
  • Numerous closely packed glands with complex,
    undulating architecture and papillary infoldings.
  • Numerous markedly dilated back to back glands
    with abundant cytoplasm and rigid luminal borders
  • Infiltrative growth pattern
  • Cytologic atypia including enlarged nuclei and
    prominent macronucleoli, amphophilic cytoplasm
    and blue mucin
  • Majority represent Gleason pattern 3
  • IHC Very USEFUL provide objective
    support/evidence

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Pseudohyperplastic CarcinomaImmunohistochemistry
  • Negative with basal markers
  • AMACR slightly lower sensitivity
  • (70-77) for this variant compared to
    conventional PCa

9
Pseudohyperplastic CarcinomaSignificance
  • Uncommon variant of PCa
  • Diagnostic challenge on NBX
  • Critical not to
  • Under-diagnose this variant as benign ( IHC
    useful)
  • Over-diagnose in minute foci as HGPIN cannot be
    ruled out with certainty. (IHC may not be very
    useful in this setting)

10
Case 2
  • 55 Y , PSA 5.0
  • H/O Minute focus of Prostate adenocarcinoma,
    Gleason score 6, lt5 of biopsy
  • Underwent Radical Prostatectomy

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Case 2
  • Diagnosis
  • Prostate adenocarcinoma with atrophic features,
    Gleason score 336.

13
Prostate cancer, Atrophic Variant
  • Unusual variant, confused with benign acinar
    atrophy
  • Incidence NBX 2, Rad Pros 3
  • Resemble atrophy or PAH on low-power
  • (due to scant cytoplasm) but has cytologic
    atypia of malignancy

Egan et al, AJSP, 1997
14
Prostate cancer, Atrophic VariantDiagnostic
Criteria
  • Abnormal architecture is subtle due to scant
    cytoplasm
  • Rare in a pure form conventional PCA is
    typically present
  • Infiltrative architecture
  • Round, often dilated acini, lined by falltened
    attenuated epithelium with scant cytoplasm and
    high N/C ratio
  • Cytologic atypia (nuclear) beyond that seen in
    atrophy
  • Scant cytoplasm compared to conventional PCa,
    less amphophilic
  • Acini commonly show blue mucin and/or
    eosinophilic secretions

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Basal marker
P504S
19
Prostate cancer, Atrophic VariantImmunohistochemi
stry
  • Basal markers negative
  • AMACR lower sensitivity (70) for this variant
    compared to conventional PCa

20
Prostate cancer, Atrophic VariantSignificance
  • Uncommon
  • Significant diagnostic pitfall in NBX
  • Crticial not to under-diagnose as benign
  • Majority are Gleason score 6, (few Gleason score
    7).

21
Case 3
  • 73Y African-American
  • S/P radiation therapy for prostate adenocarcinoma
  • (Gleason score 6, diagnosed in 2004)

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Case 3
  • Diagnosis
  • Prostate adenocarcinoma
  • Well-differentiated mimicking adenosis
  • Morphologically resembles Gleason score 6 with
    minimal therapy change

25
Adenosis
  • Incidence NBX 0.8
  • Common in TURP as incidental finding

26
Adenosis vs. Well-Diff PCaDiagnostic Criteria
  • ADENOSIS
  • Well circumscribed,lobular
  • Similar-appearing small glands mixed with large
    glands
  • Occasional glands with recognizable basal cell on
    HE
  • Pale clear cytoplasm
  • Small nucleoli
  • Blue mucin rare
  • Basal cells present on IHC ( may be patchy)
  • WELL-DIFFERENTIATED PCA
  • Haphazard, disorganized growth
  • Small glands appear different from large glands
  • Basal cells not recognized on HE
  • Occasional amphophilic cytoplasm
  • Occasional large prominent nucleoli
  • Blue mucin common
  • Basal cells absent

Epstein 2008
27
Adenosis
28
Adenosis vs. Well-Diff PCa
  • Constellation of features outweigh the
    significance of any one feature
  • Adenosis 19 show some infiltration
  • 40 show prominent nucleoli
  • Well-Diff PCa 30 lack prominent nucleoli
  • Both Crowded glands, crystalloids,
    AMACR positivity

29
Well-Differentiated PCa mimicking Adenosis
30
Case 4
  • 85Y H/O hematuria
  • Prostatic urethral mass on cystoscopy

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Case 4
  • Diagnosis
  • Prostatic Duct Adenocarcinoma
  • Behave like Gleason score 448

34
Prostatic duct adenocarcinoma
  • Incidence 0.4-0.8 of PCa
  • Frequently admixed with PCa showing acinar
    differentiation
  • Can arise in large primary peri-urethral
    prostatic ducts
  • Exophytic papillary lesions
  • Obstructive symptoms, hematuria
  • Can arise in peipheral prostatic ducts

35
Prostatic duct adenocarcinomaDiagnostic criteria
  • Papillary fronds with fibrovascular cores
  • Lined by pseudostratified columnar epithelium
    with abundant amphophilic cytoplasm

36
Prostatic duct adenocarcinoma
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Prostatic duct adenocarcinomaDiagnostic criteria
  • Papillary fronds with fibrovascular cores
  • Lined by pseudostratified columnar epithelium
    with abundant amphophilic cytoplasm
  • Cribriform pattern formed by back to back large
    glands lined by pseudostratified columnar
    epithelium with intraglandular bridging and
    slit-like lumens
  • No Basal cells present

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Prostatic duct adenocarcinomaSignificance
  • Diagnostic pitfall in NBX
  • Mild cytologic atypia without prominent
    nucleoli
  • Tumor fragmentation
  • DD Prostatic urethral polyp
  • HGPIN

41
Prostatic Urethral Polyp
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Prostatic Duct AdenocarcinomaSignificance
  • Diagnostic pitfall in TUR
  • DD may mimic high-grade papillary urothelial
    carcinoma
  • Nuclear features useful
  • UC nuclei pleomorphic vs. monotonous nuclei of
    PCa
  • IHC Very useful
  • PCa PSA ,CK903 p63 , CK 7
  • UC PSA -, CK 903 p63 ,CK 7

44
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