Journal of Pathology and Translational Medicine

Sun-Jae Lee

2 Articles

Cytopathologic Features of Secretory Carcinoma of Salivary Gland: Report of Two Cases: Young Ah Kim, Jae Won Joung, Sun-Jae Lee, Hoon-Kyu Oh, Chang Ho Cho, Woo Jung Sung; J Pathol Transl Med. 2019;53(1):70-74. Published online December 28, 2018; DOI: https://doi.org/10.4132/jptm.2018.11.09

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Secretory carcinoma of the salivary gland (SC) is a newly introduced rare salivary gland tumor that shares histological, immunohistochemical, and genetic characteristics with secretory carcinoma of the breast. Here, we report the cytologic features of two cases of SC confirmed by surgical resection. In these two cases, SC was incidentally detected in a 64-year-old female and a 56-yearold male. Fine needle aspiration cytology revealed nests of tumor cells with a papillary or glandular structure floating in mucinous secretions. The tumor cells demonstrated uniform, round, smooth nuclear contours and distinct nucleoli. Multiple characteristic cytoplasmic vacuoles were revealed. Singly scattered tumor cells frequently showed variable sized cytoplasmic vacuoles. The cytopathologic diagnosis of SC should be considered when characteristic cytological findings are revealed. Further immunohistochemistry and gene analyses are helpful to diagnose SC.

Citations

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Salivary Gland Secretory Carcinoma; Review of 13 Years World‐Wide Experience and Meta‐Analysis
Eyal Yosefof, Tomer Boldes, Daniel Dan, Eyal Robenshtok, Yulia Strenov, Gideon Bachar, Thomas Shpitzer, Aviram Mizrachi
The Laryngoscope.2024; 134(4): 1716. CrossRef
Efficacy of Fine-Needle Aspiration Cytology in Diagnosing Secretory Carcinoma of Salivary Gland: A Systematic Review and Meta-Analysis
Pooja Sharma Kala, Mamta Gupta, Naveen Thapliyal
Acta Cytologica.2024; 68(2): 83. CrossRef
An Underappreciated Cytomorphological Feature of Secretory Carcinoma of Salivary Gland on Fine Needle Aspiration Biopsy: Case Report with Literature Review
Yinan Hua, Bing Leng, Kenneth E. Youens, Lina Liu
Head and Neck Pathology.2022; 16(2): 567. CrossRef
Prognostic factors in mammary analogue secretory carcinomas of the parotid gland: Systematic review and meta‐analysis
Stefan Janik, Muhammad Faisal, Blazen Marijić, Stefan Grasl, Matthaeus Ch. Grasl, Gregor Heiduschka, Boban M. Erovic
Head & Neck.2022; 44(3): 792. CrossRef
A systematic review of secretory carcinoma of the salivary gland: where are we?
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Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology.2021; 132(4): e143. CrossRef
Clinical characteristics of acinic cell carcinoma and secretory carcinoma of the parotid gland
Tetsuya Terada, Ryo Kawata, Keiki Noro, Masaaki Higashino, Shuji Nishikawa, Shin-ichi Haginomori, Yoshitaka Kurisu, Hiroko Kuwabara, Yoshinobu Hirose
European Archives of Oto-Rhino-Laryngology.2019; 276(12): 3461. CrossRef

A Rare Case of Intramural Müllerian Adenosarcoma Arising from Adenomyosis of the Uterus: Sun-Jae Lee, Ji Y. Park; J Pathol Transl Med. 2017;51(4):433-440. Published online June 29, 2017; DOI: https://doi.org/10.4132/jptm.2017.06.11

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Abstract PDF

Müllerian adenosarcomas usually arise as polypoid masses in the endometrium of post-menopausal women. Occasionally, these tumors arise in the cervix, vagina, broad and round ligaments, ovaries and rarely in extragenital sites; these cases are generally associated with endometriosis. We experienced a rare case of extraendometrial, intramural adenosarcoma arising in a patient with adenomyosis. A 40-year-old woman presented with sudden-onset suprapubic pain. The imaging findings suggested leiomyoma with cystic degeneration in the uterine fundus. An ill-defined ovoid tumor with hemorrhagic degeneration, measuring 7.5 cm in diameter, was detected. The microscopic findings showed glandular cells without atypia and a sarcomatous component with pleomorphism and high mitotic rates. There was no evidence of endometrial origin. To recognize that adenosarcoma can, although rarely, arise from adenomyosis is important to avoid overstaging and inappropriate treatment.

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International Journal of Surgery.2024;[Epub] CrossRef
Mullerian adenosarcoma accidentally detected and coexisting with cervical carcinoma in situ: a rare case report
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Mucinous carcinoma originating from uterine adenomyosis: a case report
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Journal of Medical Case Reports.2023;[Epub] CrossRef
Endometrial Cancer Arising in Adenomyosis (EC-AIA): A Systematic Review
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Case Report: Uterine Adenosarcoma With Sarcomatous Overgrowth and Malignant Heterologous Elements
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Frontiers in Medicine.2022;[Epub] CrossRef
Adenomyosis as a Risk Factor for Myometrial or Endometrial Neoplasms—Review
Maria Szubert, Edward Kozirog, Jacek Wilczynski
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Uterine adenosarcoma arising from a subserosal adenomyoma: A case report
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Uterine Adenosarcoma Originating in Adenomyosis: Report of an Extremely Rare Phenomenon and Review of Published Literature
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Uterine adenosarcoma. Report of 5 cases and review of literature
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