Morphologic features in a series of 352 Spitz melanocytic proliferations help predict their oncogenic drivers
Autor: | Mahtab Samimi, Julien Jacquemus, Daniel Pissaloux, Franck Tirode, Arnaud de la Fouchardière, Thibault Kervarrec, Christine Castillo |
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Přispěvatelé: | Département d'anatomopathologie, biopathologie, Centre Léon Bérard [Lyon], Département de Pathologie [CHRU Tours], Université Francois Rabelais [Tours]-Centre Hospitalier Régional Universitaire de Tours (CHRU TOURS), Infectiologie et Santé Publique (UMR ISP), Université de Tours-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE), Centre de Recherche en Cancérologie de Lyon (UNICANCER/CRCL), Centre Léon Bérard [Lyon]-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Service de dermatologie (CHRU de Tours), Centre Hospitalier Régional Universitaire de Tours (CHRU TOURS), Cypath : siège social [Villeurbanne], Université Francois Rabelais [Tours]-Centre Hospitalier Régional Universitaire de Tours (CHRU Tours), Université de Tours (UT)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE), Université de Lyon-Université de Lyon-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM), Centre Hospitalier Régional Universitaire de Tours (CHRU Tours) |
Jazyk: | angličtina |
Rok vydání: | 2021 |
Předmět: |
Proto-Oncogene Proteins B-raf
Morphology Pathology medicine.medical_specialty Skin Neoplasms Spitz naevus Carcinogenesis Biology MAP3K8 Pathology and Forensic Medicine Oncogenic driver 03 medical and health sciences 0302 clinical medicine Stroma Proto-Oncogene Proteins medicine ROS1 Humans Child Fusion Molecular Biology Cellular atypia 030304 developmental biology 0303 health sciences Melanoma Receptor Protein-Tyrosine Kinases Cell Biology General Medicine Protein-Tyrosine Kinases medicine.disease 030220 oncology & carcinogenesis Spitz melanocytic proliferation Immunohistochemistry [SDV.MHEP.DERM]Life Sciences [q-bio]/Human health and pathology/Dermatology |
Zdroj: | Virchows Archiv Virchows Archiv, Springer Verlag, In press, ⟨10.1007/s00428-021-03227-x⟩ |
ISSN: | 0945-6317 1432-2307 |
DOI: | 10.1007/s00428-021-03227-x⟩ |
Popis: | International audience; Spitz nevi are indolent melanocytic tumors arising preferentially during and after childhood. Over the last decades, recurrent oncogenic drivers, sparsely detected in melanoma, were identified in Spitz melanocytic proliferations. Therefore, the detection of such drivers appears as a relevant diagnostic tool to distinguish both entities. Interestingly, morphologic features might correlate with the oncogenic drivers. Thus, the goal of this study was to assess the performances of previously identified morphological criteria to predict the presence of specific drivers. In total, 352 Spitz melanocytic proliferations either with a genetically identified oncogenic driver or investigated for ALK, ROS1, and NTRK1 overexpression by immunohistochemistry were enrolled in the present study. The microscopic features of the cases were assessed blindly with regards to the molecular status and, performances of previously described morphological criteria to predict the molecular status were assessed applying the likelihood-ratio test (LHR). Overall, an oncogenic driver was identified in 76% of the cases (n = 268/352). No microscopic features allowed the reliable prediction of ROS1- and NTRK1-overexpressing cases. By contrast, a plexiform pattern can contribute to the recognition of ALK-overexpressing cases (LHR(+) = 6.14). Importantly, the pseudo-schwannoma variant was highly suggestive of NTRK3-rearranged cases (LHR(+) = 43). Moreover, atypical/malignant tumor (LHR(+) = 5.18), severe cellular atypia (LHR(+) = 5.07), and p16 loss (LHR(+) = 14) contribute to the recognition of MAP3K8-rearranged cases, while the presence of a sheet-like architecture (LHR(+) = 5.39) and a marked fibrosis of the stroma (LHR(+)=5.06) were predictive of BRAF-fused tumors. To conclude, our study confirms ALK-overexpressing, NTRK3-, MAP3K8-, and BRAF-rearranged cases harbored distinct morphologic features allowing their microscopic recognition. |
Databáze: | OpenAIRE |
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