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Study on the morphology and reproducibility of the diagnosis of endometrial lesions utilizing liquid‐based cytology
Author(s) -
Papaefthimiou Maria,
Symiakaki Hera,
Mentzelopoulou Panagiota,
Tsiveleka Ageliki,
Kyroudes Aspasia,
Voulgaris Zannis,
Tzonou Anastasia,
Karakitsos Petros
Publication year - 2005
Publication title -
cancer cytopathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.052
H-Index - 304
eISSN - 1097-0142
pISSN - 0008-543X
DOI - 10.1002/cncr.21025
Subject(s) - medicine , atypia , cytology , endometrial hyperplasia , endometrial cancer , liquid based cytology , gynecology , radiology , hyperplasia , curettage , atypical hyperplasia , cancer , pathology , cervical cancer
BACKGROUND The objective of the current study was to determine the diagnostic cytomorphologic criteria for liquid‐based cytology and to evaluate the reproducibility and usefulness of the cytologic diagnosis in endometrial lesions. METHODS A total of 162 direct endometrial samplings taken from postmenopausal women were evaluated by 2 skilled cytopathologists in endometrial cytology. The cytologic diagnosis was made according to the 1994 classification scheme of the World Health Organization. After establishment of the criteria, three additional cytopathologists without any experience in liquid‐based endometrial cytology examined the same cases to determine interobserver variability. The intraobserver variability also was evaluated by all the observers. RESULTS The cytomorphologic criteria were established in the following four diagnostic categories: atrophic endometrium, hyperplasia without atypia, hyperplasia with atypia, and adenocarcinoma. The overall interobserver agreement was nearly perfect with a κ value of 0.89 during the checking round and ranged from moderate to substantial with κ values of 0.48–0.80, respectively, in the other diagnostic rounds ( P < 0.0001); hyperplasia with atypia was found to be the most difficult category to identify correctly. Furthermore, the intraobserver agreement ranged from substantial to perfect with κ values of 0.61–1.00 in all diagnostic rounds ( P < 0.0001). CONCLUSIONS Liquid‐based cytology allows for standardized and reproducible endometrial preparations, which in turn allows the application of common diagnostic criteria among cytopathologists. Furthermore, liquid‐based cytology in combination with endometrial sampling could be a useful tool for the outpatient diagnosis of endometrial lesions, which could reduce unnecessary curettage. Cancer (Cancer Cytopathol) 2005. © 2005 American Cancer Society.

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