TY - JOUR
T1 - The clinicopathologic spectrum and genomic landscape of de-/trans-differentiated melanoma
AU - Ferreira, Ingrid
AU - Droop, Alastair
AU - Edwards, Olivia
AU - Wong, Kim
AU - Harle, Victoria
AU - Habib, Omar
AU - Gharpuray-Pandit, Deepa
AU - Houghton, Joseph
AU - Wiedemeyer, Katharina
AU - Mentzel, Thomas
AU - Billings, Steven D.
AU - Ko, Jennifer S.
AU - Fuzesi, Laszlo
AU - Mulholland, Kathleen
AU - Prusac, Ivana Kuzmic
AU - Liegl-Atzwanger, Bernadette
AU - Aubain, Nicolas de Saint
AU - Caldwell, Helen
AU - Riva, Laura
AU - van der Weyden, Louise
AU - Arends, Mark J
AU - Brenn, Thomas
AU - Adams, David J
PY - 2021/6/21
Y1 - 2021/6/21
N2 - 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 7 patients with available follow-up data (median follow-up period of 25 months; range: 8-36 months), 2 died from their disease and 3 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 were 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 the 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.
AB - 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 7 patients with available follow-up data (median follow-up period of 25 months; range: 8-36 months), 2 died from their disease and 3 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 were 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 the 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.
KW - dedifferentiated melanoma
KW - transdifferentiated melanoma
KW - melanoma with heterologous transdifferentiation
KW - melanoma with divergent transdifferentiation
KW - matplastic melanoma
KW - melanoma
KW - dedifferentiation
KW - transdifferentiation
KW - rhabdomyosarcomatous
KW - epthelial
KW - NF1
KW - CASZ1
U2 - 10.1038/s41379-021-00857-z
DO - 10.1038/s41379-021-00857-z
M3 - Article
JO - Modern Pathology
JF - Modern Pathology
SN - 0893-3952
ER -