Ascites production and prognosis after ventriculoperitoneal shunt for diffuse midline gliomas in children: A case

Chunxia Huang1, Xubin Chai2,3, Yunpeng Han1

  • 1Department of Clinical Laboratory, Guangdong Sanjiu Brain Hospital, Guangzhou, China.

Medicine
|October 28, 2024
PubMed

Insights

Diffuse midline glioma (DMG) patients with hydrocephalus treated with shunts can develop malignant ascites. Continuous monitoring of cerebrospinal fluid (CSF) and ascitic fluid is crucial for early detection and intervention.

Area of Science:

  • Neuro-oncology
  • Pediatric neurosurgery
  • Cancer metastasis

Background:

  • Diffuse midline glioma (DMG) is an aggressive pediatric brain tumor.
  • Hydrocephalus is a common complication of DMG, often managed with ventriculoperitoneal shunts (VPS).
  • VPS can lead to ascites, a serious concern in patients with brain tumors.

Purpose of the Study:

  • To report on pediatric cases of diffuse midline glioma (DMG) with H3 K27M mutation.
  • To describe the development of carcinomatous ascites following VPS insertion in these patients.
  • To highlight the importance of monitoring for metastatic spread via ascitic fluid.

Main Methods:

  • Case series of 3 pediatric patients with brainstem DMG (H3 K27M mutation).
  • All patients developed hydrocephalus requiring VPS insertion.
  • Post-operative development of malignant ascites with confirmed tumor cells in ascitic fluid.

Main Results:

  • All 3 patients developed intra-abdominal metastasis manifesting as carcinomatous ascites.
  • Initial response of primary tumors and hydrocephalus to treatment was observed.
  • Despite palliative chemotherapy, all patients succumbed within one month of ascites development.

Conclusions:

  • These cases highlight the critical need for vigilant monitoring of both CSF and ascitic fluid in DMG patients.
  • Regular biochemical and cytologic analysis of fluids aids in early detection of disease progression.
  • Proactive monitoring and timely intervention are essential for potentially improving outcomes in pediatric glioma patients.
Abstract

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