2016
DOI: 10.1111/cyt.12354
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Fine needle aspiration cytology of a nodal low‐grade serous neoplasm: a case report of low‐grade serous carcinoma arising from a serous borderline tumour with cyto‐histological correlation

Abstract: This case report describes a rare case of nodal low grade serous pelvic neoplasia. Together with histological correlation, it illustrates previously undocumented cytomorphological features and also discusses important differential diagnosis and potential pitfalls for misdiagnosis.

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Cited by 3 publications
(3 citation statements)
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References 13 publications
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“…A few previous reports have briefly described cytological findings in LGSC, but none have provided detailed descriptions 8–10 . Our cytological examination of LGSC revealed isolated atypical epithelial cells and variable cellular clusters of sheet‐like, tubular, papillary, and micropapillary structures.…”
Section: Discussionmentioning
confidence: 71%
See 1 more Smart Citation
“…A few previous reports have briefly described cytological findings in LGSC, but none have provided detailed descriptions 8–10 . Our cytological examination of LGSC revealed isolated atypical epithelial cells and variable cellular clusters of sheet‐like, tubular, papillary, and micropapillary structures.…”
Section: Discussionmentioning
confidence: 71%
“…3 A few previous reports have briefly described cytological findings in LGSC, but none have provided detailed descriptions. [8][9][10] Our cytological examination of LGSC revealed isolated atypical epithelial cells and variable cellular clusters of sheet-like, tubular, papillary, and micropapillary structures. LGSC cells are usually small-to-mediumsized and have a high nuclear-to-cytoplasmic content ratio, nuclei with small irregularities, increased coarse chromatin, and prominent nucleoli.…”
Section: Discussionmentioning
confidence: 99%
“…2d). Therefore, such findings should be reported as a "low-grade serous neoplasm" rather than a low-grade serous carcinoma [21,22]. To support one's diagnosis, immunohistochemistry for claudin-4 (positive in epithelial tumors), PAX-8, ER, and progesterone receptor (PR) (positive in tumors of Mullerian origin), WT-1 (typically diffusely positive in these tumors of serous lineage), in addition to p53 and p16, can be employed [11,13,17].…”
Section: Differential Diagnosismentioning
confidence: 99%