The Journal of Urology
Volume 175, Issue 2 , Pages 495-499, February 2006

Virtual Microscopy in Prostate Histopathology: Simultaneous Viewing of Biopsies Stained Sequentially With Hematoxylin and Eosin, and α-Methylacyl-Coenzyme A Racemase/p63 Immunohistochemistry

  • Henrik O. Helin

      Affiliations

    • Institute of Medical Technology, University of Tampere, Tampere
  • ,
  • Mikael E. Lundin

      Affiliations

    • Biomedical Informatics Group, HUSLAB, Helsinki University Central Hospital, Helsinki
  • ,
  • Mervi Laakso

      Affiliations

    • Department of Pathology, Seinäjoki Central Hospital, Seinäjoki, Finland
  • ,
  • Johan Lundin

      Affiliations

    • Biomedical Informatics Group, HUSLAB, Helsinki University Central Hospital, Helsinki
  • ,
  • Heikki J. Helin

      Affiliations

    • Department of Oncology, University of Helsinki and Division of Pathology, HUSLAB, Helsinki University Central Hospital, Helsinki
  • ,
  • Jorma Isola

      Affiliations

    • Institute of Medical Technology, University of Tampere, Tampere
    • Corresponding Author InformationCorrespondence: Institute of Medical Technology, 33014 University of Tampere, Tampere, Finland (telephone: +358-3-2156729; FAX: +358-3-2158923)

Received 17 February 2005

Purpose

Histopathological diagnosis of small focus carcinomas in prostatic needle biopsies is often assisted by IHC. To make a definitive diagnosis the pathologist must compare IHC findings with hematoxylin and eosin stained tissue morphology. We introduce what is to our knowledge a new application of virtual microscopy, in which hematoxylin and eosin, and IHC stains done sequentially on the same microscope slide can be simultaneously displayed and compared on a computer screen.

Materials and Methods

A total of 30 hematoxylin and eosin stained prostatic needle biopsies were scanned with a computer controlled microscope. The slides were destained and then immunostained with a cocktail of AMACR and p63 antibodies, which labels the nuclei of nonmalignant basal cells (p63) and the cytoplasm of neoplastic glandular cells suspicious for malignancy (AMACR). The slides were then scanned again and the pairs of virtual slides were aligned for synchronized viewing.

Results

The presented technique was found helpful when suspicious lesions were small and when examining the immunoprofile of specimens was warranted, in addition to examining hematoxylin and eosin stained tissue morphology. The usefulness of our approach based on virtual microscopy can be evaluated on the website http://www.webmicroscope.net/AMACRp63, which also serves as an educational tool for self-learning the correlation between hematoxylin and eosin stained tissue morphology, and AMACR/p63 IHC in prostate biopsies.

Conclusions

The technology for simultaneously viewing sequentially hematoxylin and eosin and IHC stained prostate biopsies can be readily used for educational purposes, as exemplified by our website, and along with the availability of rapid virtual slide scanners it can also be used for clinical diagnostics.

Key Words:  prostate , prostatic neoplasms , biopsy , alpha-methylacyl-CoA racemase , telepathology

Abbreviations and Acronyms:  AMACR, α-methylacyl-coenzyme A racemase , ASAP, atypical small acinar proliferation , IHC, immunohistochemistry , PIN, prostatic intraepithelial neoplasia , ROI, region of interest

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 Supported by grants from the Scientific Foundation of Instrumentarium, Inc., Finska Läkaresällskapet, Biomedicum Foundation, Medicinska Understödsföreningen Liv och Hälsa, Svenska Kulturfonden, Finnish Cancer Foundation and Sigfrid Juselius Foundation.

PII: S0022-5347(05)00164-3

doi:10.1016/S0022-5347(05)00164-3

The Journal of Urology
Volume 175, Issue 2 , Pages 495-499, February 2006