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The World Health Organization 2016 classification of testicular germ cell tumours: a review and update from the International Society of Urological Pathology Testis Consultation Panel
Authors:Sean R Williamson  Brett Delahunt  Cristina Magi‐Galluzzi  Ferran Algaba  Lars Egevad  Thomas M Ulbright  Satish K Tickoo  John R Srigley  Jonathan I Epstein  Daniel M Berney  the Members of the ISUP Testicular Tumour Panel
Affiliation:1. Department of Pathology and Laboratory Medicine and Josephine Ford Cancer Institute, Henry Ford Health System, Detroit, MI, USA;2. Wayne State University School of Medicine, Detroit, MI, USA;3. Department of Pathology and Molecular Medicine, Wellington School of Medicine and Health Sciences, University of Otago—Wellington, Wellington, New Zealand;4. Robert J. Tomsich Pathology and Laboratory Medicine Institute, Cleveland Clinic, Cleveland, OH, USA;5. Section of Pathology, Fundació Puigvert, Universitat Autónoma de Barcelona, Barcelona, Spain;6. Department of Pathology, Karolinska University Hospital, Stockholm, Sweden;7. Department of Pathology and Laboratory Medicine, Indiana University, Indianapolis, IN, USA;8. Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA;9. Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario, Canada;10. Department of Pathology, The Johns Hopkins Hospital, Baltimore, MD, USA;11. Department of Molecular Oncology, Barts Cancer Institute, Queen Mary University of London, London, UK
Abstract:Since the last World Health Organization (WHO) classification scheme for tumours of the urinary tract and male genital organs, there have been a number of advances in the understanding, classification, immunohistochemistry and genetics of testicular germ cell tumours. The updated 2016 draft classification was discussed at an International Society of Urological Pathology Consultation on Testicular and Penile Cancer. This review addresses the main updates to germ cell tumour classification. Major changes include a pathogenetically derived classification using germ cell neoplasia in situ (GCNIS) as a new name for the precursor lesion, and the distinction of prepubertal tumours (non‐GCNIS‐derived) from postpubertal‐type tumours (GCNIS‐derived), acknowledging the existence of rare benign prepubertal‐type teratomas in the postpubertal testis. Spermatocytic tumour is adopted as a replacement for spermatocytic seminoma, to avoid potential confusion with the unrelated usual seminoma. The spectrum of trophoblastic tumours arising in the setting of testicular germ cell tumour continues to expand, to include epithelioid and placental site trophoblastic tumours analogous to those of the gynaecological tract. Currently, reporting of anaplasia (seminoma or spermatocytic tumour) or immaturity (teratoma) is not required, as these do not have demonstrable prognostic importance. In contrast, overgrowth of a teratomatous component (somatic‐type malignancy) and sarcomatous change in spermatocytic tumour indicate more aggressive behaviour, and should be reported.
Keywords:germ cell neoplasia in situ  germ cell tumour  postpubertal‐type teratoma  spermatocytic tumour
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