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Developmentally anomalous cerebellar encephalocele arising within the cerebellopontine angle and extending into the adjacent skull base in a pediatric patient

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A Correction to this article was published on 04 November 2021

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Abstract

Lesions of the cerebellopontine angle (CPA) in young children are rare, with the most common being arachnoid cysts and epidermoid inclusion cysts. The authors report a case of an encephalocele containing heterotopic cerebellar tissue arising from the right middle cerebellar peduncle and filling the right internal acoustic canal in a 2-year-old female patient. Her initial presentation included a focal left 6th nerve palsy. Magnetic resonance imaging was suggestive of a high-grade tumor of the right CPA. The lesion was removed via a retrosigmoid approach, and histopathologic analysis revealed heterotopic atrophic cerebellar tissue. This report is the first description of a heterotopic cerebellar encephalocele within the CPA and temporal skull base of a pediatric patient.

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Acknowledgments

We thank Arie Perry, MD, at the University of California, San Francisco, for assistance with pathological analysis in this case and Kristin Kraus, MSc, for editorial assistance.

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Correspondence to Samuel H. Cheshier.

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The original online version of this article was revised due to a retrospective Open Access cancellation.

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Hamrick, F.A., Karsy, M., Bruggers, C.S. et al. Developmentally anomalous cerebellar encephalocele arising within the cerebellopontine angle and extending into the adjacent skull base in a pediatric patient. Childs Nerv Syst 37, 2943–2947 (2021). https://doi.org/10.1007/s00381-020-05020-8

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  • DOI: https://doi.org/10.1007/s00381-020-05020-8

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