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Interpretation of fine-needle aspirates processed by the Thin Prep® technique: Cytologic artifacts and diagnostic pitfalls. Presented in part at the 46th Annual scientific Meeting of the American Society of Cytopathology, Nashville, Tennessee, November 3–7, 1998.

dc.contributor.authorMichael, Claire W.en_US
dc.contributor.authorHunter, Brianen_US
dc.date.accessioned2006-04-19T14:22:28Z
dc.date.available2006-04-19T14:22:28Z
dc.date.issued2000-07en_US
dc.identifier.citationMichael, Claire W.; Hunter, Brian (2000)."Interpretation of fine-needle aspirates processed by the Thin Prep® technique: Cytologic artifacts and diagnostic pitfalls. Presented in part at the 46th Annual scientific Meeting of the American Society of Cytopathology, Nashville, Tennessee, November 3–7, 1998. ." Diagnostic Cytopathology 23(1): 6-13. <http://hdl.handle.net/2027.42/35306>en_US
dc.identifier.issn8755-1039en_US
dc.identifier.issn1097-0339en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/35306
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=10907924&dopt=citationen_US
dc.description.abstractThe improvement in quality of cytologic preparations with the use of the ThinPrep® methodology has been well-documented, but the cytologic artifacts resulting from this technique have not been adequately described. This study describes and illustrates the cytologic artifacts introduced by the ThinPrep technique when used on fine-needle aspirates (FNAs), and evaluates these artifacts as potential diagnostic pitfalls. We reviewed a total of 120 FNAs simultaneously processed by both conventional smears and ThinPrep. FNAs were obtained from the following sites: lymph node (27), breast (23), soft-tissue sites (20), salivary glands (13), gastrointestinal tract (10), lung (9), thyroid gland (13), liver (3), adrenal gland (1), and kidney (1). The ThinPrep smears were consistently devoid of obscuring elements, and the cells were adequately preserved and evenly dispersed. However, we noted some cytomorphologic alterations that should be recognized to avoid erroneous diagnoses. The size of cell clusters was decreased, large branching sheets were fragmented, and there were more single cells, resulting in apparent discohesion. Small cells such as lymphocytes tended to aggregate. All cells were generally smaller and occasionally spindled, the chromatin detail was attenuated, and nucleoli were more prominent. Intranuclear inclusions were difficult to visualize. Background matrix was often altered in both quantity and quality. Extracellular particles, small mononuclear cells, red blood cells, and myoepithelial cells were markedly decreased in number. The pathologist should be cautious in interpreting FNAs prepared using ThinPrep if that is the only methodology employed. Familiarity with artifacts is essential to avoid misinterpretations. Diagn. Cytopathol. 23:6–13, 2000. © 2000 Wiley-Liss, Inc.en_US
dc.format.extent732689 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherJohn Wiley & Sons, Inc.en_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherCancer Research, Oncology and Pathologyen_US
dc.titleInterpretation of fine-needle aspirates processed by the Thin Prep® technique: Cytologic artifacts and diagnostic pitfalls. Presented in part at the 46th Annual scientific Meeting of the American Society of Cytopathology, Nashville, Tennessee, November 3–7, 1998.en_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPathologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Pathology, University of Michigan, Ann Arbor, Michigan ; Department of Pathology, University of Michigan, 1500 E. Medical Center Drive, Room 2G332/Box 0054, Ann Arbor, MI 48109-0054en_US
dc.contributor.affiliationumDepartment of Pathology, University of Michigan, Ann Arbor, Michiganen_US
dc.identifier.pmid10907924en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/35306/1/2_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/1097-0339(200007)23:1<6::AID-DC2>3.0.CO;2-Fen_US
dc.identifier.sourceDiagnostic Cytopathologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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