Publication: Well-differentiated fetal adenocarcinoma of the lung mimicking adenoid cystic carcinoma on fine needle aspiration: A case report
Issued Date
2016-11-01
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ISSN
10970339
87551039
87551039
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2-s2.0-84978164213
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Mahidol University
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SCOPUS
Bibliographic Citation
Diagnostic Cytopathology. Vol.44, No.11 (2016), 917-920
Suggested Citation
Vilasinee Rerkpichaisuth, Jennifer A. Collins, Thiraphon Boonyaarunnate, Syed Z. Ali Well-differentiated fetal adenocarcinoma of the lung mimicking adenoid cystic carcinoma on fine needle aspiration: A case report. Diagnostic Cytopathology. Vol.44, No.11 (2016), 917-920. doi:10.1002/dc.23526 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/41028
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Title
Well-differentiated fetal adenocarcinoma of the lung mimicking adenoid cystic carcinoma on fine needle aspiration: A case report
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Abstract
© 2016 Wiley Periodicals, Inc. Well-differentiated fetal adenocarcinoma (WDFA) of the lung is a rare variant of adenocarcinoma with an unusual morphology. Although the histologic features of this rare neoplasm have been well established, there is a deficit in the literature with regards to its discrete cytomorphologic features. We report the fine needle aspiration (FNA) findings of a case of this unusual malignancy in a 44-year-old man with an incidental lung nodule. FNA revealed three-dimensional clusters of epithelial cells with scant cytoplasm, hyperchromatic nuclei that are associated with an extracellular metachromatic matrix. The original cytology report was signed out as an epithelial neoplasm favor adenoid cystic carcinoma. Consequently, a wedge resection of the lung was done and the histologic diagnosis was WDFA of the lung. The findings of minimal nuclear atypia in association with focally abundant spheres of extracellular matrix can mimic adenoid cystic carcinoma. WDFA has good prognosis and therefore, pre-operative cytologic diagnosis is critical to clinical management. We present the cytomorphologic features of this neoplasm with particular emphasis on a potential diagnostic pitfall of this rare entity. Diagn. Cytopathol. 2016;44:917–920. © 2016 Wiley Periodicals, Inc.