| Literature DB >> 34155350 |
Ingrid Ferreira1,2, Alastair Droop1, Olivia Edwards1, Kim Wong1, Victoria Harle1, Omar Habeeb3, Deepa Gharpuray-Pandit4, Joseph Houghton5, Katharina Wiedemeyer6,7, Thomas Mentzel8, Steven D Billings9, Jennifer S Ko9, Laszlo Füzesi10, Kathleen Mulholland11, Ivana Kuzmic Prusac12, Bernadette Liegl-Atzwanger13, Nicolas de Saint Aubain14, Helen Caldwell15, Laura Riva1, Louise van der Weyden1, Mark J Arends15, Thomas Brenn16,17,18, David J Adams1.
Abstract
Dedifferentiation and transdifferentiation are rare and only poorly understood phenomena in cutaneous melanoma. To study this disease more comprehensively we have retrieved 11 primary cutaneous melanomas from our pathology archives showing biphasic features characterized by a conventional melanoma and additional areas of de-/trans-differentiation as defined by a lack of immunohistochemical expression of all conventional melanocytic markers (S-100 protein, SOX10, Melan-A, and HMB-45). The clinical, histologic, and immunohistochemical findings were recorded and follow-up was obtained. The patients were mostly elderly (median: 81 years; range: 42-86 years) without significant gender predilection, and the sun-exposed skin of the head and neck area was most commonly affected. The tumors were deeply invasive with a mean depth of 7 mm (range: 4-80 mm). The dedifferentiated component showed atypical fibroxanthoma-like features in the majority of cases (7), while additional rhabdomyosarcomatous and epithelial transdifferentiation was noted histologically and/or immunohistochemically in two tumors each. The background conventional melanoma component was of desmoplastic (4), superficial spreading (3), nodular (2), lentigo maligna (1), or spindle cell (1) types. For the seven patients with available follow-up data (median follow-up period of 25 months; range: 8-36 months), two died from their disease, and three developed metastases. Next-generation sequencing of the cohort revealed somatic mutations of established melanoma drivers including mainly NF1 mutations (5) in the conventional component, which was also detected in the corresponding de-/trans-differentiated component. In summary, the diagnosis of primary cutaneous de-/trans-differentiated melanoma is challenging and depends on the morphologic identification of conventional melanoma. Molecular analysis is diagnostically helpful as the mutated gene profile is shared between the conventional and de-/trans-differentiated components. Importantly, de-/trans-differentiation does not appear to confer a more aggressive behavior.Entities:
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Year: 2021 PMID: 34155350 DOI: 10.1038/s41379-021-00857-z
Source DB: PubMed Journal: Mod Pathol ISSN: 0893-3952 Impact factor: 7.842