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Application of the Milan System for Reporting Submandibular Gland Cytopathology: An international, multi-institutional study

  • Zahra Maleki
  • , Zubair Baloch
  • , Ryan Lu
  • , Khurram Shafique
  • , Sharon J. Song
  • , Kartik Viswanathan
  • , Rema A. Rao
  • , Holly Lefler
  • , Aisha Fatima
  • , Austin Wiles
  • , Vickie Y. Jo
  • , He Wang
  • , Guido Fadda
  • , Celeste N. Powers
  • , Syed Z. Ali
  • , Liron Pantanowitz
  • , Momin T. Siddiqui
  • , Ritu Nayar
  • , Jerzy Klijanienko
  • , Guliz A. Barkan
  • Jeffrey F. Krane, Esther D. Rossi, Fabiano Callegari, Ivana Kholová, Massimo Bongiovanni, William C. Faquin, Marc P. Pusztaszeri
  • Johns Hopkins University
  • University of Pennsylvania
  • Cornell University
  • Northwestern University
  • Rutgers - The State University of New Jersey, New Brunswick
  • Virginia Commonwealth University
  • Brigham and Women’s Hospital
  • Catholic University of the Sacred Heart
  • University of Pittsburgh
  • Institut Curie
  • Loyola University Chicago
  • Universidade Federal de São Paulo
  • Fimlab Laboratories
  • Tampere University
  • University of Lausanne
  • Massachusetts General Hospital
  • McGill University

Research output: Contribution to journalArticlepeer-review

55 Scopus citations

Abstract

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.

Original languageEnglish
Pages (from-to)306-315
Number of pages10
JournalCancer Cytopathology
Volume127
Issue number5
DOIs
StatePublished - May 2019

Keywords

  • atypia of undetermined significance (AUS)
  • benign neoplasm
  • fine-needle aspiration (FNA)
  • malignant
  • Milan System for Reporting Salivary Gland Cytopathology (MRSSGC)
  • nondiagnostic
  • nonneoplastic
  • risk of malignancy (ROM)
  • salivary gland neoplasm of uncertain malignant potential (SUMP)
  • submandibular gland
  • suspicious for malignancy (SM)

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