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  • Oxford University Press (OUP)  (16)
  • 1
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 2008
    In:  American Journal of Clinical Pathology Vol. 130, No. 2 ( 2008-08), p. 213-218
    In: American Journal of Clinical Pathology, Oxford University Press (OUP), Vol. 130, No. 2 ( 2008-08), p. 213-218
    Type of Medium: Online Resource
    ISSN: 0002-9173 , 1943-7722
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    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2008
    detail.hit.zdb_id: 2039921-2
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  • 2
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 2021
    In:  American Journal of Clinical Pathology Vol. 155, No. 5 ( 2021-04-26), p. 638-648
    In: American Journal of Clinical Pathology, Oxford University Press (OUP), Vol. 155, No. 5 ( 2021-04-26), p. 638-648
    Abstract: The ongoing global severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic necessitates adaptations in the practice of surgical pathology at scale. Primary diagnosis by whole-slide imaging (WSI) is a key component that would aid departments in providing uninterrupted histopathology diagnosis and maintaining revenue streams from disruption. We sought to perform rapid validation of the use of WSI in primary diagnosis meeting recommendations of the College of American Pathologists guidelines. Methods Glass slides from clinically reported cases from 5 participating pathologists with a preset washout period were digitally scanned and reviewed in settings identical to typical reporting. Cases were classified as concordant or with minor or major disagreement with the original diagnosis. Randomized subsampling was performed, and mean concordance rates were calculated. Results In total, 171 cases were included and distributed equally among participants. For the group as a whole, the mean concordance rate in sampled cases (n = 90) was 83.6% counting all discrepancies and 94.6% counting only major disagreements. The mean pathologist concordance rate in sampled cases (n = 18) ranged from 90.49% to 97%. Conclusions We describe a novel double-blinded method for rapid validation of WSI for primary diagnosis. Our findings highlight the occurrence of a range of diagnostic reproducibility when deploying digital methods.
    Type of Medium: Online Resource
    ISSN: 0002-9173 , 1943-7722
    RVK:
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    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2021
    detail.hit.zdb_id: 2039921-2
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  • 3
    In: American Journal of Clinical Pathology, Oxford University Press (OUP), Vol. 155, No. 1 ( 2021-01-04), p. 87-96
    Abstract: Steatohepatitic hepatocellular carcinoma is a distinct variant of hepatocellular carcinoma strongly associated with underlying nonalcoholic steatohepatitis. The molecular biology of steatohepatitic hepatocellular carcinoma is not fully elucidated, and thus we aimed to investigate the molecular underpinnings of this entity. Methods Transcriptomic analysis using RNAseq was performed on eight tumor-nonneoplastic pairs of steatohepatitic hepatocellular carcinoma with comparison to conventional hepatocellular carcinoma transcriptomes curated in The Cancer Genome Atlas. Immunohistochemistry was used to validate key RNA-level findings. Results Steatohepatitic hepatocellular carcinoma demonstrated a distinctive differential gene expression profile compared with The Cancer Genome Atlas curated conventional hepatocellular carcinomas (n = 360 cases), indicating the distinctive steatohepatitic hepatocellular carcinoma morphology is associated with a unique gene expression profile. Pathway analysis comparing tumor-nonneoplastic pairs revealed significant upregulation of the hedgehog pathway based on GLI1 overexpression and significant downregulation of carnitine palmitoyltransferase 2 transcript. Glutamine synthetase transcript was significantly upregulated, and fatty acid binding protein 1 transcript was significantly downregulated and immunohistochemically confirmed, indicating steatohepatitic hepatocellular carcinoma tumor cells display a zone 3 phenotype. Conclusions Steatohepatitic hepatocellular carcinoma demonstrates a distinctive morphology and gene expression profile, phenotype of zone 3 hepatocytes, and activation of the hedgehog pathway and repression of carnitine palmitoyltransferase 2, which may be important in tumorigenesis.
    Type of Medium: Online Resource
    ISSN: 0002-9173 , 1943-7722
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    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2021
    detail.hit.zdb_id: 2039921-2
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  • 4
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 2010
    In:  American Journal of Clinical Pathology Vol. 133, No. 4 ( 2010-04-01), p. 623-632
    In: American Journal of Clinical Pathology, Oxford University Press (OUP), Vol. 133, No. 4 ( 2010-04-01), p. 623-632
    Abstract: We performed a histologic and immunohistochemical assessment of 53 noninvasive appendiceal epithelial proliferations, appropriating terminology and using markers shown useful in differentiating serrated colorectal polyps. These were classified as hyperplastic polyp (HP), sessile serrated adenoma (SSA), mixed serrated and adenomatous lesion (MSAL), mucinous cystadenoma (MCA), or conventional adenoma (CAD). Immunohistochemical analysis for cytokeratin (CK) 20, Ki-67, MUC6, and β-catenin was performed. Diagnoses were as follows: HP, 6; SSA, 12; HP vs SSA, 3; MSAL, 16; MCA, 14; and CAD, 2. All HPs showed expanded (beyond surface) CK20 and expanded or normal (base) Ki-67; 1 was MUC6+. Most SSAs and MSALs were CK20-expanded or expanded with random expression in deep crypts (Ex/I) and Ki-67-expanded, Ex/I (expanded with asymmetry), or normal. All SSAs and 8 of 16 MSALs were MUC6+. CADs were CK20-Ex/I, Ki-67-Ex, and MUC6–; 1 showed nuclear β-catenin expression. Serrated appendiceal lesions can be categorized using colorectal terminology. MUC6 is associated with SSA morphologic features. Similar immunohistochemical patterns in SSA and MSAL suggest a link between these lesions.
    Type of Medium: Online Resource
    ISSN: 1943-7722 , 0002-9173
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    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2010
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  • 5
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 2013
    In:  American Journal of Clinical Pathology Vol. 140, No. 6 ( 2013-12-01), p. 872-880
    In: American Journal of Clinical Pathology, Oxford University Press (OUP), Vol. 140, No. 6 ( 2013-12-01), p. 872-880
    Type of Medium: Online Resource
    ISSN: 1943-7722 , 0002-9173
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    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2013
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  • 6
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 2009
    In:  American Journal of Clinical Pathology Vol. 132, No. 4 ( 2009-10-01), p. 506-513
    In: American Journal of Clinical Pathology, Oxford University Press (OUP), Vol. 132, No. 4 ( 2009-10-01), p. 506-513
    Abstract: Endoscopic ampullectomy (EA) is increasingly used in the management of ampullary neoplasia. Although studies on the safety and efficacy of this procedure exist, no study has specifically addressed the histopathologic features of the specimens. We review our experience with 45 EA specimens assessed for the following: diagnosis, high-grade dysplasia (HGD), submucosal ampullary gland/ductule involvement, specimen integrity, and margin status. Familial adenomatous polyposis (FAP) status and the endoscopist’s impression of completeness of removal were also ascertained. Previous biopsy diagnoses were compared with ampullectomy diagnoses, and histologic and clinical features were correlated with disease persistence. The histologic features of the ampullectomy specimens were as follows: diagnosis (no diagnostic abnormality, 3; reactive, 8; adenoma, 26; adenocarcinoma, 7; other, 1); HGD, 1; submucosal ampullary gland/ductule involvement, 20; specimen integrity (intact, 22; fragmented, 23); and margin status (positive, 20; negative, 2; could not be assessed, 12). Five patients had FAP, and EA was deemed complete in 21 (47%). The diagnostic agreement between preampullectomy biopsy and ampullectomy was 64%. Of the patients, 33 (73%) had documented persistent disease. None of the histologic or clinical features had a statistically significant relationship with disease persistence.
    Type of Medium: Online Resource
    ISSN: 1943-7722 , 0002-9173
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    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2009
    detail.hit.zdb_id: 2039921-2
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  • 7
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 2021
    In:  American Journal of Clinical Pathology Vol. 156, No. 4 ( 2021-09-08), p. 607-619
    In: American Journal of Clinical Pathology, Oxford University Press (OUP), Vol. 156, No. 4 ( 2021-09-08), p. 607-619
    Abstract: The Ki-67 proliferation index is integral to gastroenteropancreatic neuroendocrine tumor (GEP-NET) assessment. Automated Ki-67 measurement would aid clinical workflows, but adoption has lagged owing to concerns of nonequivalency. We sought to address this concern by comparing 2 digital image analysis (DIA) platforms to manual counting with same-case/different-hotspot and same-hotspot/different-methodology concordance assessment. Methods We assembled a cohort of GEP-NETs (n = 20) from 16 patients. Two sets of Ki-67 hotspots were manually counted by three observers and by two DIA platforms, QuantCenter and HALO. Concordance between methods and observers was assessed using intraclass correlation coefficient (ICC) measures. For each comparison pair, the number of cases within ±0.2xKi-67 of its comparator was assessed. Results DIA Ki-67 showed excellent correlation with manual counting, and ICC was excellent in both within-hotspot and case-level assessments. In expert-vs-DIA, DIA-vs-DIA, or expert-vs-expert comparisons, the best-performing was DIA Ki-67 by QuantCenter, which showed 65% cases within ±0.2xKi-67 of manual counting. Conclusions Ki-67 measurement by DIA is highly correlated with expert-assessed values. However, close concordance by strict criteria ( & gt;80% within ±0.2xKi-67) is not seen with DIA-vs-expert or expert-vs-expert comparisons. The results show analytic noninferiority and support widespread adoption of carefully optimized and validated DIA Ki-67.
    Type of Medium: Online Resource
    ISSN: 0002-9173 , 1943-7722
    RVK:
    RVK:
    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2021
    detail.hit.zdb_id: 2039921-2
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  • 8
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 2015
    In:  American Journal of Clinical Pathology Vol. 143, No. 3 ( 2015-03-01), p. 320-324
    In: American Journal of Clinical Pathology, Oxford University Press (OUP), Vol. 143, No. 3 ( 2015-03-01), p. 320-324
    Type of Medium: Online Resource
    ISSN: 1943-7722 , 0002-9173
    RVK:
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    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2015
    detail.hit.zdb_id: 2039921-2
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  • 9
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 2011
    In:  American Journal of Clinical Pathology Vol. 135, No. 2 ( 2011-02-01), p. 238-244
    In: American Journal of Clinical Pathology, Oxford University Press (OUP), Vol. 135, No. 2 ( 2011-02-01), p. 238-244
    Type of Medium: Online Resource
    ISSN: 1943-7722 , 0002-9173
    RVK:
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    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2011
    detail.hit.zdb_id: 2039921-2
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  • 10
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 2008
    In:  American Journal of Clinical Pathology Vol. 129, No. 3 ( 2008-03), p. 367-376
    In: American Journal of Clinical Pathology, Oxford University Press (OUP), Vol. 129, No. 3 ( 2008-03), p. 367-376
    Type of Medium: Online Resource
    ISSN: 0002-9173 , 1943-7722
    RVK:
    RVK:
    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2008
    detail.hit.zdb_id: 2039921-2
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