Jerzy Klijanienko

Prof. Jerzy Klijanienko

orcid

Research Focus & Metrics

Academic Career Length

34Years (1993-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 November 2019 in European Journal of Cancer
Verified
Journal Article
Closed access
CLCharlotte Lecerf
Charlotte Lecerf
MKMaud Kamal
Maud Kamal
SVSophie VACHER
Sophie VACHER
WCWalid Chemlali
Walid Chemlali
ASAnne Schnitzler
Anne Schnitzler
Christophe Le TourneauChristophe Le Tourneau
Christophe Le Tourneau

16 August 1999 in Diagnostic Cytopathology
Verified
Journal Article
Closed access
PDF file
JKJerzy Klijanienko
Jerzy Klijanienko
AEAdel K. El-Naggar
Adel K. El-Naggar
PVPhilippe Vielh
Philippe Vielh

3 May 2019 in Cancer Cytopathology
Verified
Journal Article
Open access
PDF file
ZMZahra Maleki
Zahra Maleki
ZBZubair Baloch
Zubair Baloch
RLRyan Lu
Ryan Lu
KSKhurram Shafique
Khurram Shafique
SSSharon J. Song
Sharon J. Song
Marc PusztaszeriMarc Pusztaszeri
Marc Pusztaszeri
Background: The Milan System for Reporting Salivary Gland Cytopathology (MSRSGC) is a 6‐tier diagnostic category system with associated risks of malignancy (ROMs) and management recommendations. Submandibular gland fine‐needle aspiration (FNA) is uncommon with a higher frequency of inflammatory lesions and a higher relative proportion of malignancy, and this may affect the ROM and subsequent management. This study evaluated the application of the MSRSGC and the ROM for each diagnostic category for 734 submandibular gland FNAs.Methods: Submandibular gland FNA cytology specimens from 15 international institutions (2013‐2017) were retrospectively assigned to an MSRSGC diagnostic category as follows: nondiagnostic, nonneoplastic, atypia of undetermined significance (AUS), benign neoplasm, salivary gland neoplasm of uncertain malignant potential (SUMP), suspicious for malignancy (SM), or malignant. A correlation with the available histopathologic follow‐up was performed, and the ROM was calculated for each MSRSGC diagnostic category.Results: The case cohort of 734 aspirates was reclassified according to the MSRSGC as follows: nondiagnostic, 21.4% (0%‐50%); nonneoplastic, 24.2% (9.1%‐53.6%); AUS, 6.7% (0%‐14.3%); benign neoplasm, 18.3% (0%‐52.5%); SUMP, 12% (0%‐37.7%); SM, 3.5% (0%‐12.5%); and malignant, 13.9% (2%‐31.3%). The histopathologic follow‐up was available for 333 cases (45.4%). The ROMs were as follows: nondiagnostic, 10.6%; nonneoplastic, 7.5%; AUS, 27.6%; benign neoplasm, 3.2%; SUMP, 41.9%; SM, 82.3%; and malignant, 93.6%.Conclusions: This multi‐institutional study shows that the ROM of each MSRSGC category for submandibular gland FNA is similar to that reported for parotid gland FNA, although the reported rates for the different MSRSGC categories were variable across institutions. Thus, the MSRSGC can be reliably applied to submandibular gland FNA.

30 June 1999 in Diagnostic Cytopathology
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Journal Article
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JKJerzy Klijanienko
Jerzy Klijanienko
AEAdel K. El-Naggar
Adel K. El-Naggar
PVPhilippe Vielh
Philippe Vielh

17 March 2014 in Cancer Cytopathology
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Journal Article
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JKJerzy Klijanienko
Jerzy Klijanienko
PCPierre Colin
Pierre Colin
JCJérôme Couturier
Jérôme Couturier
RLRéal Lagacé
Réal Lagacé
PFPaul Fréneaux
Paul Fréneaux
STStamatios Theocharis
Stamatios Theocharis

24 June 2016 in Diagnostic Cytopathology
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Journal Article
Closed access
PDF file
JKJerzy Klijanienko
Jerzy Klijanienko
CTChristophe Le Tourneau
Christophe Le Tourneau
JRJosé Rodriguez
José Rodriguez
MCMartial Caly
Martial Caly
STStamatios Theocharis
Stamatios Theocharis