Spitz tumor with SQSTM1::NTRK2 fusion: a clinicopathological study of 5 casesShow others and affiliations
2023 (English)In: American journal of dermatopathology, ISSN 0193-1091, E-ISSN 1533-0311, Vol. 45, no 5, p. 306-310Article in journal (Refereed) Published
Abstract [en]
Spitz tumors are melanocytic neoplasms characterized by specific, mutually exclusive driver molecular events, namely genomic rearrangements involving the threonine kinase BRAF and the tyrosine kinase receptors ALK , NTRK1 , NTRK2 , NTRK3 , MET , RET , ROS1 , and MAP3K8 or less commonly, mutations in HRAS or MAP2K1 . We hereby report 5 Spitz tumors with a SQSTM1::NTRK2 fusion. All patients were woman with the ages at diagnosis ranging from 30 to 50 years. Locations included the lower extremity (n = 3), forearm, and back (one each). All the neoplasms were superficial melanocytic proliferation with a flat to dome-shaped silhouette, in which junctional spindled and polygonal dendritic melanocytes were mainly arranged as horizontal nests associated with conspicuous lentiginous involvement of the follicular epithelium. Only one case showed heavily pigmented, vertically oriented melanocytic nests resembling Reed nevus. A superficial intradermal component observed in 2 cases appeared as small nests with a back-to-back configuration. In all lesions, next-generation sequencing analysis identified a SQSTM1::NTRK2 fusion. A single case studied with fluorescence in situ hybridization for copy number changes in melanoma-related genes proved negative. No further molecular alterations were detected, including TERT-p hotspot mutations.
Place, publisher, year, edition, pages
Wolters Kluwer, 2023. Vol. 45, no 5, p. 306-310
Keywords [en]
Spitz tumor, SQSTM1::NTRK2 fusion, polygonal, dendritic, adnexal involvement, necrotic keratinocytes, Kamino bodies
National Category
Cell and Molecular Biology
Identifiers
URN: urn:nbn:se:umu:diva-207694DOI: 10.1097/DAD.0000000000002410ISI: 000974834600008PubMedID: 36939120Scopus ID: 2-s2.0-85152973859OAI: oai:DiVA.org:umu-207694DiVA, id: diva2:1753687
2023-04-282023-04-282023-09-05Bibliographically approved