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The Morpho-Molecular Landscape of Spitz Neoplasms

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MDPI
DOI: 10.3390/ijms23084211

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Spitz nevus; atypical Spitz tumor; malignant Spitz tumor; HRAS; ALK; ROS1; RET; MET; NTRK1; NTRK2; NTRK3

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Spitz neoplasms are a heterogeneous group of melanocytic proliferations with variable histological characteristics. Recent discoveries have provided insight into the molecular landscape of Spitz lineage, identifying specific molecular events that correlate with distinct histological features. Detection of driver genetic alterations can help identify aggressive subtypes requiring further molecular investigations.
Spitz neoplasms are a heterogeneous group of melanocytic proliferations with a great variability in the histological characteristics and in the biological behavior. Thanks to recent discoveries, the morpho-molecular landscape of Spitz lineage is becoming clearer, with the identification of subtypes with recurrent features thus providing the basis for a more solid and precise tumor classification. Indeed, specific mutually exclusive driver molecular events, namely HRAS or MAP2K1 mutations, copy number gains of 11p, and fusions involving ALK, ROS, NTRK1, NTRK2, NTRK3, MET, RET, MAP3K8, and BRAF genes, correlate with distinctive histological features. The accumulation of further molecular aberrations, instead, promotes the increasing malignant transformation of Spitz neoplasms. Thus, the detection of a driver genetic alteration can be achieved using the appropriate diagnostic tests chosen according to the histological characteristics of the lesion. This allows the recognition of subtypes with aggressive behavior requiring further molecular investigations. This review provides an update on the morpho-molecular correlations in Spitz neoplasms.

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