Nuclear pseudoinclusions as a clue for NUTM1-rearranged poroid tumours recognition
- PMID: 38715411
- DOI: 10.1111/his.15208
Nuclear pseudoinclusions as a clue for NUTM1-rearranged poroid tumours recognition
References
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- Kervarrec T, Pissaloux D, Tirode F et al. Gene fusions in poroma, porocarcinoma and related adnexal skin tumours: An update. Histopathology 2024; 84; 266–278.
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- Sekine S, Kiyono T, Ryo E et al. Recurrent YAP1‐MAML2 and YAP1‐NUTM1 fusions in poroma and porocarcinoma. J. Clin. Invest. 2019; 129; 3827–3832.
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- Macagno N, Kervarrec T, Sohier P et al. NUT is a specific immunohistochemical marker for the diagnosis of YAP1‐NUTM1‐rearranged cutaneous poroid neoplasms. Am. J. Surg. Pathol. 2021; 45; 1221–1227.
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- Kervarrec T, Pissaloux D, Paindavoine S et al. Recurrent PAK2 rearrangements in poroma with folliculo‐sebaceous differentiation. Histopathology 2023; 83; 310–319.
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- Kervarrec T, Frouin E, Collin C et al. Distinct regulations driving YAP1 expression loss in poroma, porocarcinoma and RB1‐deficient skin carcinoma. Histopathology 2023; 82; 885–898.
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