Malignant congenital tumor of the pineal gland rudiment. Literature review and clinical case

We present a clinical case of an extremely rare congenital brain tumor in a 6-month-old child – pineal anlage tumor (PAT), which occurs in 0.04 % of all brain neoplasms in childhood. Foreign literature describes 20 cases of PAT in children, while there are no such publications in the domestic literature. At present, this tumor is not yet defined as a separate type in the latest edition of the WHO classification in 2021. In the WHO classification of 2007, PAT is described as a rare variant of pineoblastoma with melanotic, cartilaginous and/or rhabdomyoblast differentiation, characterized by heterogeneous elements of neuroepithelial and ectomesenchymal tissue, but without endodermal structures. Due to the rarity of this type of neoplasm, histologic diagnosis can be difficult for the morphologist. Specific therapy has not been developed at present, the optimal treatment is the maximal complete surgical removal of the volumetric neoplasm, as well as polychemotherapy according to the protocol of pineoblastoma treatment. However, the efficacy of this strategy remains unclear.

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Publication Details

Journal
Russian Journal of Pediatric Hematology and Oncology
Published
2025-04-23
DOI
https://doi.org/10.21682/2311-1267-2025-12-1-70-76
Primary Topic
Glioma Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
0.00
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article

Malignant congenital tumor of the pineal gland rudiment. Literature review and clinical case

М. И. Лившиц, M. A. Kolcheva, A. N. Kislyakov, R. Kh. Anders et al.
Russian Journal of Pediatric Hematology and Oncology
Glioma Diagnosis and Treatment
article

Malignant congenital tumor of the pineal gland rudiment. Literature review and clinical case

М. И. Лившиц, M. A. Kolcheva, A. N. Kislyakov, R. Kh. Anders, P. V. Lobankin, Andrey Levashov, С. Р. Варфоломеева, Э. В. Кумирова, G. E. Chmutin, В.В. Горев, В. В. Семенова, Т. В. Наседкина, A. S. Kucheryavaya, G. A. Bykova
article en

Abstract

We present a clinical case of an extremely rare congenital brain tumor in a 6-month-old child – pineal anlage tumor (PAT), which occurs in 0.04 % of all brain neoplasms in childhood. Foreign literature describes 20 cases of PAT in children, while there are no such publications in the domestic literature. At present, this tumor is not yet defined as a separate type in the latest edition of the WHO classification in 2021. In the WHO classification of 2007, PAT is described as a rare variant of pineoblastoma with melanotic, cartilaginous and/or rhabdomyoblast differentiation, characterized by heterogeneous elements of neuroepithelial and ectomesenchymal tissue, but without endodermal structures. Due to the rarity of this type of neoplasm, histologic diagnosis can be difficult for the morphologist. Specific therapy has not been developed at present, the optimal treatment is the maximal complete surgical removal of the volumetric neoplasm, as well as polychemotherapy according to the protocol of pineoblastoma treatment. However, the efficacy of this strategy remains unclear.

Russian Journal of Pediatric Hematology and OncologyVol. 12(1)
Engelhardt Institute of Molecular Biology (RU), Peoples' Friendship University of Russia (RU), Pirogov Russian National Research Medical University (RU), Ministry of Health (ES), Russian Children's Clinical Hospital (RU), Ministry of Health of the Russian Federation (RU), Regional Children's Clinical Hospital No. 1 (RU), National Medical Research Center of Cardiology (RU)
Openalex Percentile: Top 74%
Glioma Diagnosis and Treatment
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