Abstract:ObjectiveWe aimed to develop and reinforce a clinical management regimen for atypical endometrial cell (ATEC) categories within the descriptive reporting format for endometrial cytology.MethodsBetween January 2013 and December 2014, 215 samples, for which histological examination was performed immediately or within 3 months after cytology, were cytologically diagnosed as ATEC. For these samples, the medical records were retrospectively reviewed to identify risk factors for malignancy.ResultsAmong 152 samples d… Show more
“…The new terminology for endometrial cytology has been introduced and now TYSEC system is usefully utilized. [1][2][3][4][5] However, diagnosis of gray zone category, ATEC, especially ATEC-US implies that clinicians would perform unnecessary biopsies. Accurate cytological diagnosis is required to maximize the merit of cytology, which seems less harmful than biopsy.…”
Section: Discussionmentioning
confidence: 99%
“…Recent studies have shown that nearly 10% of the cases assigned to cytological ATEC-US category had corresponding malignant histology. [3][4][5] Although cytological gray zone category intrinsically has some amount of corresponding malignant histology, if it is large, it could cause a problem for managing patients with a cytological diagnosis of ATEC-US. Therefore, it would be ideal to minimize the number of cytological diagnosis of ATEC.…”
Background: The Yokohama System of Endometrial Cytology has been used for reporting endometrial cytology, which includes gray zone category, atypical endometrial cells (ATEC), subdivided into ATEC-US and ATEC-AE. ATEC-US has been reported to be correlated with malignancy in nearly 10% of the cases. For accurate diagnosis, application of ancillary techniques on endometrial cytology was investigated.Methods: Thirty-seven liquid based cytological specimens (SurePath™) with diagnosis of ATEC or malignant which have corresponding histological specimens, were subjected to immunocytochemical analysis for β-catenin, ARID1A, and PTEN. Hot spots of mutations for KRAS, BRAF and PIK3CA were evaluated by using i-densy system (ARKRAY).Results: In endometrial samples with the diagnosis of ATEC and malignant, aberrant gene expressions and/or gene mutations for β-catenin, ARID1A, PTEN, KRAS, BRAF,
“…The new terminology for endometrial cytology has been introduced and now TYSEC system is usefully utilized. [1][2][3][4][5] However, diagnosis of gray zone category, ATEC, especially ATEC-US implies that clinicians would perform unnecessary biopsies. Accurate cytological diagnosis is required to maximize the merit of cytology, which seems less harmful than biopsy.…”
Section: Discussionmentioning
confidence: 99%
“…Recent studies have shown that nearly 10% of the cases assigned to cytological ATEC-US category had corresponding malignant histology. [3][4][5] Although cytological gray zone category intrinsically has some amount of corresponding malignant histology, if it is large, it could cause a problem for managing patients with a cytological diagnosis of ATEC-US. Therefore, it would be ideal to minimize the number of cytological diagnosis of ATEC.…”
Background: The Yokohama System of Endometrial Cytology has been used for reporting endometrial cytology, which includes gray zone category, atypical endometrial cells (ATEC), subdivided into ATEC-US and ATEC-AE. ATEC-US has been reported to be correlated with malignancy in nearly 10% of the cases. For accurate diagnosis, application of ancillary techniques on endometrial cytology was investigated.Methods: Thirty-seven liquid based cytological specimens (SurePath™) with diagnosis of ATEC or malignant which have corresponding histological specimens, were subjected to immunocytochemical analysis for β-catenin, ARID1A, and PTEN. Hot spots of mutations for KRAS, BRAF and PIK3CA were evaluated by using i-densy system (ARKRAY).Results: In endometrial samples with the diagnosis of ATEC and malignant, aberrant gene expressions and/or gene mutations for β-catenin, ARID1A, PTEN, KRAS, BRAF,
“…21 However, several studies showed that increasing number of cases in gray zone category, especially ATEC-US in TYSEC, could cause problem in managing patients. [22][23][24] To solve the problem, a new approach to improve diagnostic accuracy have been expected. accuracy of endometrial carcinoma using thin-layer samples.…”
Section: Diagnostic Classification Of Endometrial Cytologymentioning
confidence: 99%
“…In order to improve diagnostic accuracy by standardization, sophisticated diagnostic algorithm by using LBC, the Osaki Study Group (OSG) method, was introduced as a reliable and reproducible method by a Japanese group 21 . However, several studies showed that increasing number of cases in gray zone category, especially ATEC‐US in TYSEC, could cause problem in managing patients 22–24 . To solve the problem, a new approach to improve diagnostic accuracy have been expected.…”
Background
Endometrial cytology is not much popular in the world, but is commonly used in a few countries. Although cytomorphological evaluation of endometrial cytology is complicating, recent advance in technology helps improve diagnostic accuracy. In addition, new reporting system, The Yokohama System, has been introduced as a standard reporting system resembling The Bethesda System of the uterine cervical cytology. Although sample standardization is one of the causes in diagnostic problem, it was solved by liquid‐based cytology (LBC) technology. In addition, standardized diagnostic algorithm by cytomorphological assessment of LBC samples, the Osaki Study Group (OSG) method, was recently proposed as a reliable and reproducible method. LBC can be utilized for ancillary methods. Application of immunocytochemistry and molecular technology on endometrial cytology samples has been studied to improve diagnostic accuracy. Recent progress of molecular technology has revealed many driver gene mutations in endometrial cancer and its precursors. Surprisingly, many studies revealed that even normal endometrial tissue had driver gene mutations.
Conclusion
Based on the recent advance in knowledge of molecular profile of endometrial lesions and normal endometrial tissue, endometrial cytology will gain much power in clinical usefulness.
“…Endometrial cancer is one of the common gynecological malignancies that threaten women's health, 1,2 especially for women in the perimenopausal and postmenopausal period, 3 and the incidence rate has been on the rise in recent years. Atypical endometrial hyperplasia (AEH) is the precancerous lesion for EC, and its pathological morphological manifestation is similar to that of highly differentiated EC 4,5 . The co‐incidence rate for AEH and EC were 15–55%, 6 and they are similar in clinical treatments and surgical methods.…”
Objectives
To evaluate shear wave elastography (SWE) technology diagnosis value of endometrial cancer (EC) and atypical endometrial hyperplasia (AEH), and to establish predictive logistic regression models for the diagnosis of EC and AEH.
Methods
Clinical information collection, transvaginal conventional ultrasonography, and SWE check were performed on 122 patients, who were perimenopausal or postmenopausal vaginal bleeding with ≥4.5 mm thick endometrium. The maximal (Emax) and mean (Emean) of Young's modulus for the endometrium were obtained. Using pathology as the gold standard, ROC curves were plotted to evaluate Young's modulus on the diagnostic effectiveness of EC and AEH. Single‐factor analysis and bivariate logistic regression methods were applied to assess the clinical variables, transuaginal conventional ultrasonography variables, and Young's modulus on the identification of EC and AEH.
Results
Out of 122 cases of endometrial lesions, 85 cases were benign lesions, and the remaining 37 cases were EC and AEH. The Emax and Emean for the benign group were 29.80 ± 11.40 and 17.96 ± 8.05 kPa, respectively. The Emax and Emean values for EC and AEH group were 59.49 ± 16.95 and 38.46 ± 17.10 kPa, respectively. Emax and Emean for both groups were statistically significant, with p <.001. In the logistical regression analysis, endometrial thickness, Color score, and Young's modulus were identified as independent risk factors for EC and AEH.
Conclusions
SWE technology plays an important role in the diagnosis of EC and AEH, and the diagnostic effectiveness would be higher when combined with conventional ultrasonography.
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