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Pineal anlage tumor: a case report and review of the literature

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Abstract

Purpose

Pineal anlage tumors (PAT) are extremely rare malignant tumors in the pediatric population considered to be a variant of pineoblastomas. These tumors are characterized by a combination of neuroectodermal and heterologous ectomesenchymal components. PAT can be clinically aggressive and has a propensity to cerebrospinal fluid (CSF) dissemination. So far, only 13 cases of these tumors have been reported in the literature.

Case Article

In this article, we report the case of an anlage tumor in a 3-year-old girl with a rapidly aggressive course.

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Abbreviations

CNS:

Central nervous system

CSF:

Cerebrospinal fluid

CT:

Computerized tomography

MNTI:

Melanotic neuroectodermal tumor of childhood

MRI:

Magnetic resonance imaging

PAT:

Pineal anlage tumor

WHO:

World Health Organization

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Correspondence to Eduardo Cambruzzi.

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Cambruzzi, E., Medeiros, M.S., da Silva, J.N.A.M. et al. Pineal anlage tumor: a case report and review of the literature. Childs Nerv Syst 38, 1625–1629 (2022). https://doi.org/10.1007/s00381-021-05441-z

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  • DOI: https://doi.org/10.1007/s00381-021-05441-z

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