Introduction: Conventional cell blocks (CCB) prepared from cytological specimens are very useful but the method is relatively time-consuming. Suitable modifications in cell-block techniques are beneficial for improving the turnaround time. We share our experience of a rapid microwave cell-block (MCB) technique.
Aim And Objectives: To study the quality of routine and immunohistochemical (IHC) staining of cell-block sections from serous body fluids prepared by the MCB technique compared with the CCB technique.
Method: A total of 177 serous body fluid samples were processed by routine centrifugation technique, and the sediments were used for cell-block preparations by both conventional and rapid microwave methods. Cell-block sections were stained with haematoxylin and eosin stain. Haematoxylin and eosin staining quality was analysed using three parameters (cellularity, morphology and staining intensity). IHC for epithelial membrane antigen and calretinin were also performed, and the quality of staining was evaluated on 62/177 samples. Results were analysed using appropriate statistical tests.
Results: The time taken for processing cell blocks by the MCB method was 1 hour and 18 minutes compared to 13 hours and 45 minutes by CCB. The quality of sections by both methods showed good agreement for cellularity and intensity of staining, and moderate agreement for morphology. A 100% concordance was noted for distinguishing benign and malignant samples on morphology as well as with IHC stain results.
Conclusion: Although the techniques are comparable in terms of quality of routine and IHC staining, we recommend using the MCB technique due to its short turnaround time.
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http://dx.doi.org/10.1111/cyt.12909 | DOI Listing |
Cytopathology
January 2021
Department of Pathology, Jawaharlal Institute of Postgraduate Medical Education and Research (JIPMER), Puducherry, India.
Introduction: Conventional cell blocks (CCB) prepared from cytological specimens are very useful but the method is relatively time-consuming. Suitable modifications in cell-block techniques are beneficial for improving the turnaround time. We share our experience of a rapid microwave cell-block (MCB) technique.
View Article and Find Full Text PDFDiagn Cytopathol
June 2007
Mahatma Gandhi Institute of Medical Sciences, Sevagram, Wardha, Maharashtra, India.
Cell blocks have largely been neglected in cervical cytology. The aim of this study was to determine if microwave processed cell blocks prepared from residual material on sampling devices could add to the diagnostic accuracy of cervico-vaginal smears. The material remaining on the spatula after making cervical smears was rinsed in ethanol and used to prepare microwave-processed cell blocks in 260 patients.
View Article and Find Full Text PDFCancer
February 2002
Department of Pathology, Pamela Youde Nethersole Eastern Hospital, Hong Kong, China.
Background: Thyroid transcription factor-1 (TTF-1) is a homeodomain-containing transcription factor selectively expressed in thyroid, lung and diencephalon. It has been shown to label pulmonary adenocarcinoma, thyroid tumors, and small cell carcinoma (pulmonary and extrapulmonary) with relatively high sensitivity and specificity. The usefulness of this immunostain in cytology specimens has not been thoroughly discussed in the literature.
View Article and Find Full Text PDFDiagn Cytopathol
September 2001
Cytopathology Section, National Institutes of Health/National Cancer Institute, Bethesda, Maryland 20892-1500, USA.
The distinction of mesothelial cells in cytologic samples is often a diagnostic challenge. This is particularly true in potentially malignant effusions in which reactive mesothelial cells may simulate adenocarcinoma (ACA) cells, and in the differentiation of ACA vs. mesothelioma.
View Article and Find Full Text PDFCancer
June 1999
Cytopathology Section, Laboratory of Pathology, National Institutes of Health/National Cancer Institute, Bethesda, Maryland 20892-1500, USA.
Background: Anti-alpha-inhibin, an antibody directed against a peptide hormone, has been shown to be a useful diagnostic aid in surgical pathology material for the identification of sex cord-stromal neoplasms and recently has been described in adrenocortical carcinoma (ACC). The diagnosis of ACC versus renal cell carcinoma (RCC) may be difficult morphologically, particularly in fine-needle aspiration (FNA) material. To date, the immunohistochemical distinction of ACC from RCC is based on a panel of antibodies that include vimentin, cytokeratins, and epithelial membrane antigen.
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