Tumors from the 2nd spinal nerve in childhood. Review of publications and a clinical case from practice

Neoplasms of the C2 spinal nerves are rare clinical observations in childhood. The removal of these tumors has a number of features related to their localization. The paper describes the experience of treating a 17-year-old child with a tumor (schwannoma) of the C2 spinal nerve. In the patient, the manifestation of the disease was associated with manifestations of compression myelopathy against the background of a large tumor detected by MRI at the level of C1-C2 vertebrae with an extra-intracanal spread of the “hourglass” type. Despite the size of the tumor and the location of the intramural component ventrally from the spinal cord, the chosen tactics made it possible to minimize surgical trauma and avoid neurological deficit with total removal of the neoplasm.

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Publication Details

Journal
Russian Journal for Personalized Medicine
Published
2024-08-08
DOI
https://doi.org/10.18705/2782-3806-2024-4-3-262-267
Primary Topic
Neurofibromatosis and Schwannoma Cases
Type
article
Field-Weighted Citation Impact
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article

Tumors from the 2nd spinal nerve in childhood. Review of publications and a clinical case from practice

К. А. Самочерных, К. В. Сысоев, N. K. Samochernykh
Russian Journal for Personalized Medicine
Neurofibromatosis and Schwannoma Cases
article

Tumors from the 2nd spinal nerve in childhood. Review of publications and a clinical case from practice

К. А. Самочерных, К. В. Сысоев, N. K. Samochernykh
article en

Abstract

Neoplasms of the C2 spinal nerves are rare clinical observations in childhood. The removal of these tumors has a number of features related to their localization. The paper describes the experience of treating a 17-year-old child with a tumor (schwannoma) of the C2 spinal nerve. In the patient, the manifestation of the disease was associated with manifestations of compression myelopathy against the background of a large tumor detected by MRI at the level of C1-C2 vertebrae with an extra-intracanal spread of the “hourglass” type. Despite the size of the tumor and the location of the intramural component ventrally from the spinal cord, the chosen tactics made it possible to minimize surgical trauma and avoid neurological deficit with total removal of the neoplasm.

Russian Journal for Personalized MedicineVol. 4(3)
Federal Almazov North-West Medical Research Centre (RU)
Good health and well-being
Openalex Percentile: Top 80%
Neurofibromatosis and Schwannoma Cases
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