Endobronchial ultrasound-guided fine-needle aspiration and liquid-based thin-layer cytology

Background: Optimal management of patients with lung cancer requires accurate cell typing of tumours and staging at the time of diagnosis. Endobronchial ultrasound-guided lymph node aspiration as a method of diagnosing and staging lung cancer is a relatively new technique. Aim: To report the use of...

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Published inJournal of clinical pathology Vol. 60; no. 4; pp. 388 - 391
Main Authors Wallace, W A H, Monaghan, H M, Salter, D M, Gibbons, M A, Skwarski, K M
Format Journal Article
LanguageEnglish
Published London BMJ Publishing Group Ltd and Association of Clinical Pathologists 01.04.2007
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Summary:Background: Optimal management of patients with lung cancer requires accurate cell typing of tumours and staging at the time of diagnosis. Endobronchial ultrasound-guided lymph node aspiration as a method of diagnosing and staging lung cancer is a relatively new technique. Aim: To report the use of liquid-based-thin-layer cytology for the processing and reporting of these specimens. Methods: The specimens obtained from 80 patients were processed using the ThinPrep system, with the remainder of the samples being processed as a cell block. Results: 40 of the 81 procedures yielded malignant cells (30 non-small cell carcinoma, 8 small-cell carcinoma and 2 combined small-cell carcinoma/non-small-cell carcinoma). The cell blocks were found to contain sufficient material to allow the immunohistochemical characterisation of tumour cells with a range of antibodies. Conclusion: The use of liquid-based-thin-layer cytological techniques provides high-quality specimens for diagnostic purposes. When used in conjunction with cell blocks, sufficient material may be obtained to allow immunohistochemical studies to confirm the tumour cell type. Given the current move towards centralisation of pathology services, this approach gives the pathologist high-quality specimens without the need for direct onsite support at the time of the procedure.
Bibliography:href:jclinpath-60-388.pdf
istex:BE1A344E187B2EC59ABAAF3726F6E927FBD1ED84
PMID:16816170
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Correspondence to:
 Dr W A H Wallace
 Department of Pathology, Royal Infirmary of Edinburgh, 51 Little France Crescent, Edinburgh EH16 4SA, UK; william.wallace@luht.scot.nhs.uk
local:0600388
ObjectType-Article-1
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ISSN:0021-9746
1472-4146
DOI:10.1136/jcp.2006.038901