Pineal parenchymal tumors of intermediate differentiation: in need of a stringent definition to avoid confusion. Scientific commentary on ‘Genetical and epigenetical profiling identifies two subgroups of pineal parenchymal tumors of intermediate differentiation (PPTID) with distinct molecular, histological and clinical characteristics’
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Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s00401-024-02684-3.pdf
Reference10 articles.
1. Fevre-Montange M, Szathmari A, Champier J, Mokhtari K, Chretien F, Coulon A et al (2008) Pineocytoma and pineal parenchymal tumors of intermediate differentiation presenting cytologic pleomorphism: a multicenter study. Brain Pathol 18:354–359. https://doi.org/10.1111/j.1750-3639.2008.00128.x
2. Jouvet A, Saint-Pierre G, Fauchon F, Privat K, Bouffet E, Ruchoux MM et al (2000) Pineal parenchymal tumors: a correlation of histological features with prognosis in 66 cases. Brain Pathol 10:49–60. https://doi.org/10.1111/j.1750-3639.2000.tb00242.x
3. Kleihues P, Cavenee WK (2000) World Health Organization Classification of Tumours—Pathology and Genetics. Tumours of the Nervous System, 3rd edn. International Agency for Research on Cancer, Lyon
4. Lee JC, Mazor T, Lao R, Wan E, Diallo AB, Hill NS et al (2019) Recurrent KBTBD4 small in-frame insertions and absence of DROSHA deletion or DICER1 mutation differentiate pineal parenchymal tumor of intermediate differentiation (PPTID) from pineoblastoma. Acta Neuropathol 137:851–854. https://doi.org/10.1007/s00401-019-01990-5
5. Liu APY, Li BK, Pfaff E, Gudenas B, Vasiljevic A, Orr BA et al (2021) Clinical and molecular heterogeneity of pineal parenchymal tumors: a consensus study. Acta Neuropathol 141:771–785. https://doi.org/10.1007/s00401-021-02284-5
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