Neuropediatrics 2020; 51(02): 170-172
DOI: 10.1055/s-0039-3399528
Short Communication
Georg Thieme Verlag KG Stuttgart · New York

Unilateral Hearing Loss Due to Cochlear Nerve Involvement as Isolated Symptom of a Primary Medulloblastoma

Authors

  • Janine Magg

    1   Department of Neuropaediatrics, Developmental Neurology, Social Paediatrics, University Children's Hospital, Tübingen, Germany
  • Thomas Nägele

    2   Department of Radiology, Section of Diagnostic and Interventional Neuroradiology, Tübingen, Germany
  • Michael Alber

    1   Department of Neuropaediatrics, Developmental Neurology, Social Paediatrics, University Children's Hospital, Tübingen, Germany
  • Annette Weichselbaum

    1   Department of Neuropaediatrics, Developmental Neurology, Social Paediatrics, University Children's Hospital, Tübingen, Germany
  • Martin Ebinger

    3   General Paediatrics, Oncology/Haematology, University Children's Hospital, Tübingen, Germany
  • Martin U. Schuhmann

    4   Department of Neurosurgery, Section of Pediatric Neurosurgery, Tübingen, Germany
Weitere Informationen

Publikationsverlauf

28. Juni 2019

07. September 2019

Publikationsdatum:
07. November 2019 (online)

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Abstract

Unilateral sensorineural hearing loss is a common symptom of vestibular schwannomas in adolescent patients with neurofibromatosis type 2 or sporadic vestibular schwannomas and is often the initial clinical feature. While rare cases of sensorineural impairment presenting as vision or hearing loss due to metastatic medulloblastoma are known, hearing loss as an isolated presenting symptom of primary malignant neuroepithelial tumors of the central nervous system has not been reported in the pediatric population so far. We present two adolescents with unilateral hearing loss due to cochlear nerve dysfunction as the only symptom of a primary nonmetastatic medulloblastoma of the WNT signaling pathway family members subgroup.