Ventriculoperiotoneal shunt as potential risk factor for extraneural dissemination of atypical teratoid-rhabdoid tumor in children?

Authors

  • Filip Murn Children’s Hospital Zagreb
  • Sandro Gašpar Children’s Hospital Zagreb, Department of Radiology
  • Tonći Grmoja Children’s Hospital Zagreb, Department of Radiology
  • Filip Jadrijević-Cvrlje Children’s Hospital Zagreb, Department of Oncology and Hematology
  • Ana Tripalo-Batoš Children’s Hospital Zagreb, Department of Radiology ; Department of Radiological Technology, University of Applied Health Sciences
  • Rhea Mužar Clinical Hospital Dubrava, Clinic for Plastic, Reconstructive and Aesthetic surgery
  • Goran Roić Children’s Hospital Zagreb, Department of Radiology ; Department of Radiological Technology, University of Applied Health Sciences

DOI:

https://doi.org/10.13112/PC.2024.5

Keywords:

pediatric brain tumors, atypical teratoid rhabdoid tumor, extraneural dissemination

Abstract

An atypical teratoid-rhabdoid tumor (AT/RT) is the second most common tumor in children and 30% when diagnosed, there is already metastatic dissemination. The ventriculoperitoneal shunt is a procedure that drains excess cerebrospinal fluid (CSF) in conditions such as hydrocephalus caused by meningitis, brain tumor, or neural tube defects. We present an extremely rare case of extraneural dissemination into the abdominal cavity along ventriculoperitoneal shunt in a 4-year-old boy. This is a type of extraneural dissemination in children that has only been published once and we are the first to present in Croatia. Although is known that AT/RT is a very aggressive type of tumor in this case report we present the value of ultrasound examination as part of follow-up protocol in children with VP shunt after brain tumor resection.

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Published

2024-03-06

Issue

Section

Case Report

How to Cite

Murn, F., Gašpar, S., Grmoja, T., Jadrijević-Cvrlje, F., Tripalo-Batoš, A., Mužar, R., & Roić, G. (2024). Ventriculoperiotoneal shunt as potential risk factor for extraneural dissemination of atypical teratoid-rhabdoid tumor in children?. Paediatria Croatica, 68(1), 37-41. https://doi.org/10.13112/PC.2024.5

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