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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Source
http://dx.doi.org/10.1007/s00381-021-05441-zDOI Listing

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