Your browser doesn't support javascript.
loading
Mucoepidermoid carcinoma, acinic cell carcinoma, and adenoid cystic carcinoma on fine-needle aspiration biopsy and The Milan System: an international multi-institutional study.
Miller, James A; An, Daniel; Shafique, Khurram; Song, Sharon; Rao, Rema A; Viswanathan, Kartik; Eykman, Elizabeth; Wiles, Austin; Ali, Syed Z; Field, Andrew; Fadda, Guido; Barkan, Guliz A; Layfield, Lester J; Rossi, Esther D; Powers, Celeste N; Siddiqui, Momin T; Kholova, Ivana; Baloch, Zubair; Maleki, Zahra.
Afiliação
  • Miller JA; Division of Cytopathology, Department of Pathology, The Johns Hopkins Hospital, Baltimore, Maryland.
  • An D; Division of Cytopathology, Department of Pathology, The Johns Hopkins Hospital, Baltimore, Maryland.
  • Shafique K; Department of Pathology, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania.
  • Song S; Department of Pathology, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania.
  • Rao RA; Department of Pathology, New York Presbyterian, Weill Cornell Medicine, Pathology and Laboratory Medicine, New York, New York.
  • Viswanathan K; Department of Pathology, New York Presbyterian, Weill Cornell Medicine, Pathology and Laboratory Medicine, New York, New York.
  • Eykman E; Department of Pathology, St. Vincent Hospital, Sydney, Australia.
  • Wiles A; Department of Pathology, Virginia Commonwealth University, Richmond, Virginia.
  • Ali SZ; Division of Cytopathology, Department of Pathology, The Johns Hopkins Hospital, Baltimore, Maryland.
  • Field A; Department of Pathology, St. Vincent Hospital, Sydney, Australia.
  • Fadda G; Department of Pathology, Catholic University of Sacred Heart, Fondazione Policlinico Univeristario A, Rome, Italy.
  • Barkan GA; Department of Pathology, Loyola University Medical Center, Maywood, Illinois.
  • Layfield LJ; Department of Pathology, University of Missouri School of Medicine, Columbia, Missouri.
  • Rossi ED; Department of Pathology, Catholic University of Sacred Heart, Fondazione Policlinico Univeristario A, Rome, Italy.
  • Powers CN; Department of Pathology, Virginia Commonwealth University, Richmond, Virginia.
  • Siddiqui MT; Department of Pathology, New York Presbyterian, Weill Cornell Medicine, Pathology and Laboratory Medicine, New York, New York.
  • Kholova I; Department of Pathology, Fimlab Laboratories and Tampere University, Faculty of Medicine and Health Technology, Tampere, Finland.
  • Baloch Z; Department of Pathology, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania.
  • Maleki Z; Division of Cytopathology, Department of Pathology, The Johns Hopkins Hospital, Baltimore, Maryland. Electronic address: zmaleki1@jhmi.edu.
J Am Soc Cytopathol ; 8(5): 270-277, 2019.
Article em En | MEDLINE | ID: mdl-31104944
ABSTRACT

BACKGROUND:

We evaluated the diagnostic accuracy (DA), risk of neoplasm (RON), and risk of malignancy (ROM) for the commonly encountered malignant salivary gland tumors mucoepidermoid carcinoma (MECa), acinic cell carcinoma (ACCa), and adenoid cystic carcinoma (ADCa) applying The Milan System for Reporting Salivary Gland Cytology (MSRSGC). MATERIALS AND

METHODS:

The cytology archives from 2007 to 2017 of 9 academic institutions were searched for salivary gland FNAs for the following key words mentioned either in the principal and/or differential diagnosis MEC, ACCa, and ADCa. The original cytology diagnosis was retrospectively classified according to the MSRSGC. Patient demographics, biopsy site, and available surgical follow-up were recorded. The final analysis included only cases with surgical follow-up.

RESULTS:

A total of 212 salivary gland FNAs were included. Based on retrospective reclassification according to MSRSGC, 97 of 212 (46%) FNA cases carried a diagnosis of malignancy specific for either MECa, ACCa, or ADCa. In the remaining 115 cases, 24 of 212 (11%) were reclassified as suspicious for malignancy (SM) and 91 of 212 (43%) as salivary gland neoplasm of uncertain malignant potential (SUMP). The DA for MECa, ACCa, and ADCa was 78.7%, 75% and 89%, respectively. The RON was 100% for all 3 tumors and the ROM was 93.6% for MECa, 96.8% for ACCa, and 94.4% for ADCa.

CONCLUSIONS:

The DA of 78.7% for MECa, 75% for ACCa, and 89% for ADCa is reasonable in FNA specimens. Although the management of definitive cases of malignancy remains unchanged, the MSRSGC provides a ROM for SM and SUMP categories, which can improve patient management.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Glândulas Salivares / Neoplasias das Glândulas Salivares / Carcinoma Mucoepidermoide / Carcinoma de Células Acinares / Carcinoma Adenoide Cístico / Internacionalidade Tipo de estudo: Clinical_trials / Etiology_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: J Am Soc Cytopathol Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Glândulas Salivares / Neoplasias das Glândulas Salivares / Carcinoma Mucoepidermoide / Carcinoma de Células Acinares / Carcinoma Adenoide Cístico / Internacionalidade Tipo de estudo: Clinical_trials / Etiology_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: J Am Soc Cytopathol Ano de publicação: 2019 Tipo de documento: Article