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Comparison of ThinPrep and TriPath PREP liquid-based preparations in nongynecologic specimens: A pilot study

dc.contributor.authorMichael, Claire W.en_US
dc.contributor.authorMcConnel, Jamesen_US
dc.contributor.authorPecott, Jamesen_US
dc.contributor.authorAfify, Alaa M.en_US
dc.contributor.authorAl-Khafaji, Basim M.en_US
dc.date.accessioned2006-04-19T14:22:54Z
dc.date.available2006-04-19T14:22:54Z
dc.date.issued2001-09en_US
dc.identifier.citationMichael, Claire W.; McConnel, James; Pecott, James; Afify, Alaa M.; Al-Khafaji, Basim (2001)."Comparison of ThinPrep and TriPath PREP liquid-based preparations in nongynecologic specimens: A pilot study." Diagnostic Cytopathology 25(3): 177-184. <http://hdl.handle.net/2027.42/35308>en_US
dc.identifier.issn8755-1039en_US
dc.identifier.issn1097-0339en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/35308
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=11536442&dopt=citationen_US
dc.description.abstractThinPrep (TP) and TriPath PREP (TriP) are two liquid-based cytologic preparations that produce a thin layer of cells. This study compares the diagnostic accuracy and different cytomorphologic alterations produced by these preparations in nongynecologic specimens. Samples from 10 urines (3 urothelial carcinomas and 7 negative), 4 positive serous fluids, and 7 fine-needle aspirates (FNAs) were prepared by both techniques. FNAs represented one each of: Hashimoto's thyroiditis (HT), hyperplastic colloid nodule (HCN), Hodgkin's lymphoma, liposarcoma, chondrosarcoma, squamous-cell carcinoma (SCC) metastatic to the lymph node, and carcinoid tumor. All 5 participants, none of whom had prior knowledge of the clinical history or histologic diagnosis, reviewed and interpreted the slides. Both techniques produced a clean background and were equally accurate in urines, serous fluids, and three FNAs. TriP was slightly more accurate in four FNAs: HCN and HT where colloid and lymphocytes were better represented, SCC where keratin and malignant cells were more readily identified among lymphocytes, and carcinoid which was easier to evaluate on TriP due to less cellular shrinkage and more dispersion of cells between aggregates. TP preparations had more cell shrinkage, and the chromatin was harder to evaluate. Both techniques produced artificial aggregations of lymphocytes, but TriP had a more evenly dispersed single-cell population between aggregates, rendering them easier to evaluate for atypia. TP produced fragmentation of large sheets that were flattened, while TriP contained larger branching sheets in a three-dimensional (3-D) configuration. TP produced a true monolayer of cells that were all spread at the same plane, while in TriP the cells were spread at slightly different planes, requiring frequent focusing of the viewed plane. While both techniques are acceptable for diagnostic purposes, they both introduce new cytomorphologic alterations that pathologists need to recognize. TriP seems superior to TP in FNAs specimens where preservation of architecture and cellular integrity are important considerations. Diagn. Cytopathol. 25:177–184, 2001. © 2001 Wiley-Liss, Inc.en_US
dc.format.extent263263 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.titleComparison of ThinPrep and TriPath PREP liquid-based preparations in nongynecologic specimens: A pilot studyen_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.contributor.affiliationumDepartment of Pathology, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartment of Pathology, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationotherDepartment of Pathology, Piedmont Hospital, Atlanta, Georgiaen_US
dc.identifier.pmid11536442en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/35308/1/2033_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/dc.2033en_US
dc.identifier.sourceDiagnostic Cytopathologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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