Gene fusions in poroma, porocarcinoma and related adnexal skin tumours: An update

Author:

Kervarrec Thibault123ORCID,Pissaloux Daniel4ORCID,Tirode Franck45,de la Fouchardière Arnaud145,Sohier Pierre167,Frouin Eric18ORCID,Hamard Aymeric2,Houben Roland9,Schrama David9,Barlier Anne1011,Cribier Bernard112,Battistella Maxime113,Macagno Nicolas11014

Affiliation:

1. CARADERM, French Network of Rare Cutaneous Cancer Lille France

2. Department of Pathology University Hospital of Tours Tours France

3. ‘Biologie des infections à polyomavirus’ Team UMR1282 INRAE, University of Tours Tours France

4. Department of Biopathology Center Léon Bérard Lyon France

5. Centre Léon Bérard, Cancer Research Center of Lyon, Equipe Labellisée University of Lyon, Université Claude Bernard Lyon 1, INSERM 1052, CNRS 5286 Lyon France

6. Department of Pathology Hôpital Cochin, AP‐HP, AP‐HP Centre – Université Paris Cité Paris France

7. Faculté de Médecine University Paris Cité Paris France

8. Department of Pathology University Hospital of Poitiers, University of Poitiers, LITEC Poitiers France

9. Department of Dermatology, Venereology and Allergology University Hospital Würzburg Würzburg Germany

10. Aix‐Marseille Univ, INSERM, MMG, U1251, Marmara Institute Marseille France

11. Laboratory of Molecular Biology La Conception Hospital Marseille France

12. Clinique Dermatologique Hôpital Civil, Hôpitaux Universitaires, Université de Strasbourg Strasbourg France

13. Department of Pathology Hospital Saint‐Louis, AP‐HP, Université Paris Cité, INSERM U976 Paris France

14. Department of Pathology APHM, Timone University Hospital Marseille France

Abstract

Poroma is a benign sweat gland tumour showing morphological features recapitulating the superficial portion of the eccrine sweat coil. A subset of poromas may transform into porocarcinoma, its malignant counterpart. Poroma and porocarcinoma are characterised by recurrent gene fusions involving YAP1, a transcriptional co‐activator, which is controlled by the Hippo signalling pathway. The fusion genes frequently involve MAML2 and NUTM1, which are also rearranged in other cutaneous and extracutaneous neoplasms. We aimed to review the clinical, morphological and molecular features of this category of adnexal neoplasms with a special focus upon emerging differential diagnoses, and discuss how their systematic molecular characterisation may contribute to a standardisation of diagnosis, more accurate classification and, ultimately, refinement of their prognosis and therapeutic modalities.

Publisher

Wiley

Subject

General Medicine,Histology,Pathology and Forensic Medicine

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