Handling and reporting of pelvic lymphadenectomy specimens in prostate and bladder cancer: a web-based survey by the European Network of Uropathology
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu časopisecké články
PubMed
30604878
DOI
10.1111/his.13818
Knihovny.cz E-zdroje
- Klíčová slova
- bladder cancer, lymph node, lymphadenectomy, prostate cancer,
- MeSH
- chirurgická patologie metody normy MeSH
- internet MeSH
- lidé MeSH
- lymfadenektomie * MeSH
- lymfatické metastázy * diagnóza patologie MeSH
- nádory močového měchýře * patologie MeSH
- nádory prostaty * patologie MeSH
- odběr biologického vzorku metody normy MeSH
- průzkumy a dotazníky MeSH
- staging nádorů metody normy MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Geografické názvy
- Evropa MeSH
AIMS: Pathological evaluation of lymphadenectomy specimens plays a pivotal role in accurate lymph node (LN) staging. Guidelines standardising the gross handling and reporting of pelvic LN dissection (PLND) in prostate (PCa) and bladder (BCa) cancer are currently lacking. This study aimed to establish current practice patterns of PLND evaluation among pathologists. METHODS AND RESULTS: A web-based survey was circulated to all members of the European Network of Uropathology (ENUP), comprising 29 questions focusing on the macroscopic handling, LN enumeration and reporting of PLND in PCa and BCa. Two hundred and eighty responses were received from pathologists throughout 23 countries. Only LNs palpable at grossing were submitted by 58%, while 39% routinely embedded the entire specimen. Average LN yield from PLND was ≥10 LNs in 56% and <10 LNs in 44%. Serial section(s) and immunohistochemistry were routinely performed on LN blocks by 42% and <1% of respondents, respectively. To designate a LN microscopically, 91% required a capsule/subcapsular sinus. In pN+ cases, 72% reported the size of the largest metastatic deposit and 94% reported extranodal extension. Isolated tumour cells were interpreted as pN1 by 77%. Deposits identified in fat without associated lymphoid tissue were reported as tumour deposits (pN0) by 36% and replaced LNs (pN+) by 27%. LNs identified in periprostatic fat were included in the PLND LN count by 69%. CONCLUSION: This study highlights variations in practice with respect to the gross sampling and microscopic evaluation of PLND in urological malignancies. A consensus protocol may provide a framework for more consistent and standardised reporting of PLND specimens.
Barts Cancer Institute Queen Mary University of London London UK
Charles University Hospital Plzen Czech Republic
Cork University Hospital Cork Ireland
Erasmus MC Cancer Institute University Medical Center Rotterdam the Netherlands
Hôpital Tenon Sorbonne University Paris France
Karolinska Institute Stockholm Sweden
North Bristol NHS Trust Bristol UK
University Health Network University of Toronto Toronto ON Canada
University Hospital Basel Basel Switzerland
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