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A Protocol for Rapid Post-mortem Cell Culture of Diffuse Intrinsic Pontine Glioma DIPG
Published on: March 7, 2017
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Neonatal Respiratory Failure Caused by Congenital Diffuse Intrinsic Pontine Glioma
Katie M Satrom1, Rachel A Phelan2, Christopher L Moertel3
11 Neonatology, Department of Pediatrics, University of Minnesota Masonic Children's Hospital, Minneapolis, MN, USA.
Journal of Child Neurology
|January 25, 2017
Summary
A rare newborn diffuse intrinsic pontine glioma caused respiratory failure. Postmortem examination confirmed a high-grade astrocytoma, highlighting the aggressive nature of this pediatric brain tumor.
Area of Science:
- Pediatric Oncology
- Neuro-oncology
- Neonatal Medicine
Background:
- Diffuse intrinsic pontine glioma (DIPG) is a rare and aggressive pediatric brain tumor.
- It typically affects children between ages 5-9, making newborn presentation exceedingly rare.
- Early diagnosis and intervention are crucial for managing pediatric brain tumors.
Observation:
- A newborn presented with stridor and respiratory distress, rapidly progressing to respiratory failure.
- Cerebral magnetic resonance imaging (MRI) revealed findings consistent with diffuse intrinsic pontine glioma.
- The family opted for palliative care due to the severity of the condition.
Findings:
- The case confirmed a diagnosis of diffuse intrinsic pontine glioma in a neonate.
- Postmortem examination identified the tumor as a World Health Organization (WHO) grade III astrocytoma.
- This finding underscores the potential for aggressive brain tumors to manifest at birth.
Implications:
- This case expands the known age range for diffuse intrinsic pontine glioma presentation.
- It highlights the importance of considering rare neurological conditions in neonates with respiratory distress.
- Further research into the early-onset mechanisms of pediatric brain tumors is warranted.
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