LOT and HOT … or not. The proliferation of clinically insignificant and poorly characterised types of renal neoplasia.


Journal

Pathology
ISSN: 1465-3931
Titre abrégé: Pathology
Pays: England
ID NLM: 0175411

Informations de publication

Date de publication:
Dec 2022
Historique:
received: 03 08 2022
accepted: 09 09 2022
pubmed: 22 10 2022
medline: 25 11 2022
entrez: 21 10 2022
Statut: ppublish

Résumé

The classification of malignant tumours is influenced by both immunohistochemical and molecular genetic findings. This is highlighted in the latest World Health Organization classification of renal neoplasia, which has a tumour category of 'tumours that are molecularly defined'. This implies that the defining molecular features are integral to tumourigenesis, which may not necessarily be the case. Renal oncocytoma is recognised as a benign tumour with variable morphology and immunoexpression. A variant of these tumours is hybrid oncocytic chromophobe tumour, which has features of both oncocytoma and chromophobe renal cell carcinoma and may, on rare occasions, show malignant behaviour. Recent reports have proposed two further entities with eosinophilic cytoplasm and varying nuclear pleomorphism, designated low grade oncocytic tumour (LOT) and eosinophilic vacuolated tumour (EVT), formally known as high grade oncocytic tumour (HOT). The diagnosis of these apparently benign tumours was made on the basis of morphological and immunohistochemical features. More recently it has been claimed that the mutations in the mTOR pathway are also a diagnostic feature and it is further suggested that these mutations are key to the pathogenesis of these tumours. As is seen in oncocytoma, immunohistochemical expression of tumours included in series of LOT and EVT is variable. The mutations in the mTOR pathway, where detected, were not constant, with any combination of mTOR, TSC1 and/or TSC2 being involved. A major issue is that in many of the studies full comparative genomic hybridisation results are not presented. In addition it is well recognised that mTOR mutations are seen in a variety of renal tumours. In view of these conflicting results, the rarity of these tumours and their apparent benign nature, raises questions as to why these tumours should be considered specific entities.

Identifiants

pubmed: 36270849
pii: S0031-3025(22)00263-X
doi: 10.1016/j.pathol.2022.09.002
pii:
doi:

Substances chimiques

Biomarkers, Tumor 0
TOR Serine-Threonine Kinases EC 2.7.11.1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

842-847

Informations de copyright

Copyright © 2022 Royal College of Pathologists of Australasia. All rights reserved.

Auteurs

Hemamali Samaratunga (H)

Aquesta Uropathology, Brisbane, Qld, Australia; University of Queensland, Brisbane, Qld, Australia.

Lars Egevad (L)

Department of Oncology and Pathology, Karolinska Institutet, Stockholm, Sweden.

Michelle Thunders (M)

Department of Pathology and Molecular Medicine, Wellington School of Medicine and Health Sciences, University of Otago, Wellington, New Zealand.

Kenneth A Iczskowski (KA)

Department of Pathology, Medical School of Wisconsin, Milwaukee, WI, USA.

Theodorus van der Kwast (T)

Laboratory Medicine Program, University Health Network and Princess Margaret Cancer Center, Toronto, Canada.

Glen Kristiansen (G)

Institute of Pathology, University Clinic, Bonn, Germany.

Chin-Chen Pan (CC)

Department of Pathology, Taipei Veterans General Hospital, Taipei, Taiwan.

Katia R M Leite (KRM)

Department of Urology, Laboratory of Medical Research, University of São Paulo Medical School, São Paulo, Brazil.

Andrew Evans (A)

Department of Pathology, Mackenzie Health, Richmond Hill, Ontario, Canada.

David Clouston (D)

TissuPath, Waverley, Vic, Australia.

Diane N Kenwright (DN)

Department of Pathology and Molecular Medicine, Wellington School of Medicine and Health Sciences, University of Otago, Wellington, New Zealand.

Peter B Bethwaite (PB)

Department of Pathology and Molecular Medicine, Wellington School of Medicine and Health Sciences, University of Otago, Wellington, New Zealand; Southern Community Laboratories, Wellington, New Zealand.

Greg Malone (G)

Royal Brisbane Hospital, Brisbane, Qld, Australia.

Simon Wood (S)

Department of Urology, Princess Alexandra Hospital Brisbane, Qld, Australia.

John W Yaxley (JW)

University of Queensland, Brisbane, Qld, Australia; Wesley Hospital, Brisbane, Qld, Australia.

Brett Delahunt (B)

Aquesta Uropathology, Brisbane, Qld, Australia; Department of Pathology and Molecular Medicine, Wellington School of Medicine and Health Sciences, University of Otago, Wellington, New Zealand; Southern Community Laboratories, Wellington, New Zealand. Electronic address: brett.delahunt@otago.ac.nz.

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Classifications MeSH