CC BY-NC-ND 4.0 · Asian J Neurosurg 2023; 18(03): 698-700
DOI: 10.1055/s-0043-1774822
Clinical Images

Medulloblastoma with Subcutaneous Spread: A Rare Entity

Siddharth Srinivasan
1   Department of Neurosurgery, Kasturba Medical College, Manipal Academy of Higher Education, Manipal, Karnataka, India
,
1   Department of Neurosurgery, Kasturba Medical College, Manipal Academy of Higher Education, Manipal, Karnataka, India
,
Rajesh Nair
1   Department of Neurosurgery, Kasturba Medical College, Manipal Academy of Higher Education, Manipal, Karnataka, India
,
1   Department of Neurosurgery, Kasturba Medical College, Manipal Academy of Higher Education, Manipal, Karnataka, India
› Institutsangaben
Funding None.
 

Abstract

Medulloblastoma is the most common malignant pediatric brain tumor. Histological subclassification and adjuvant therapy have improved prognostication and outcome. Extraneural metastasis remains a poor prognostic factor and subcutaneous seeding is rarely encountered and reported in the pediatric population. We report a 3-year-old child who rapidly presented with subcutaneous seeding a month following gross total resection of his tumor.


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Medulloblastomas are the most common pediatric malignant brain tumor. Extraneural metastasis of medulloblastoma, although uncommon, has been reported before. However, medulloblastoma with subcutaneous spread is a rare entity. We report a 3-year-old child who presented with decreased conscious levels and raised intracranial pressure. Evaluation with magnetic resonance imaging of the brain was suggestive of a posterior fossa midline space occupying lesion with gross obstructive hydrocephalus. He underwent emergency suboccipital craniotomy and near total resection of the tumor. Histopathology was confirmed as World Health Organization grade 4 medulloblastoma. The child made an uneventful postoperative recovery and was discharged home. Postoperatively in 6 weeks the child presented with a tense pseudomeningocele ([Fig. 1A]) and worsening hydrocephalus. Computed tomography of the brain revealed recurrence of tumor with subcutaneous spread along the posterior fossa incision line and skin over the occipital region ([Fig. 1B]). Cytology of fluid aspirated from the collection was also positive for tumor cells. The child underwent a palliative ventriculoperitoneal shunt for the hydrocephalus. The child succumbed to the disease shortly within a week.

Zoom Image
Fig. 1 (A) Clinical image demonstrating a pseudomeningocele along the posterior fossa in an operated case of central nervous system grade 4 medulloblastoma at 6 weeks follow-up. (B) Sagittal midline image of the computed tomography brain showing the pseudomeningocoele, hydrocephalus, subcutaneous tumor deposits (red arrow).

Leptomeningeal and subarachnoid spread of medulloblastoma is well documented in literature. Incidence of extraneural metastasis is 7 to 10%.[1] Most common sites are bone, bone marrow, lymph nodes, lung, and liver.[2] The mechanisms of spread are due to perineural lymphatics and by direct seeding.[3] Hematogenous route of spread is accepted as the most likely mechanism to distant locations. Extraneural metastasis with subcutaneous spread is likely due to direct seeding and remains a poor prognostic factor even with adjuvant chemoradiation.


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Conflict of Interest

None declared.

  • References

  • 1 Maiti T, Sabharwal P, Pandey P, Devi BI. Subcutaneous metastasis in medulloblastoma: a case report and review of literature. J Pediatr Neurosci 2013; 8 (02) 168-170
  • 2 Rochkind S, Blatt I, Sadeh M, Goldhammer Y. Extracranial metastases of medulloblastoma in adults: literature review. J Neurol Neurosurg Psychiatry 1991; 54 (01) 80-86
  • 3 McComb JG, Davis RL, Isaacs Jr H, Landing BH. Medulloblastoma presenting as neck tumors in 2 infants. Ann Neurol 1980; 7 (02) 113-117

Address for correspondence

Ajay Hegde, MCh, DNB, FRCS
Department of Neurosurgery, Kasturba Medical College, Manipal Academy of Higher Education
Manipal, Karnataka, India 576104

Publikationsverlauf

Artikel online veröffentlicht:
27. September 2023

© 2023. Asian Congress of Neurological Surgeons. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)

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  • References

  • 1 Maiti T, Sabharwal P, Pandey P, Devi BI. Subcutaneous metastasis in medulloblastoma: a case report and review of literature. J Pediatr Neurosci 2013; 8 (02) 168-170
  • 2 Rochkind S, Blatt I, Sadeh M, Goldhammer Y. Extracranial metastases of medulloblastoma in adults: literature review. J Neurol Neurosurg Psychiatry 1991; 54 (01) 80-86
  • 3 McComb JG, Davis RL, Isaacs Jr H, Landing BH. Medulloblastoma presenting as neck tumors in 2 infants. Ann Neurol 1980; 7 (02) 113-117

Zoom Image
Fig. 1 (A) Clinical image demonstrating a pseudomeningocele along the posterior fossa in an operated case of central nervous system grade 4 medulloblastoma at 6 weeks follow-up. (B) Sagittal midline image of the computed tomography brain showing the pseudomeningocoele, hydrocephalus, subcutaneous tumor deposits (red arrow).