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Congenital Intracranial Teratoma—An Intractable Enigma: A Case Report and Review of Literature

  • Review Article
  • Published:
Journal of Fetal Medicine

Abstract

Congenital intracranial tumors are rare, accounting for 0.5–1.9% of pediatric tumors. Though antenatal detection rates have improved with ultrasound (US) and MRI, histopathology gives a definite diagnosis. Prognosis is guarded as there is no effective postnatal treatment. We present a fetus incidentally diagnosed with intracranial teratoma by US and MRI at 36 weeks of gestation. Elective cesarean was performed for anticipated labor dystocia. A female baby with head circumference > 99th centile was delivered. Due to the invasive growth potential of the tumor, the baby succumbed at 4 months of palliative care. Further research is required for devising new treatment modalities to tackle this intractable condition.

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No funding was received from any source to support the publication of this case report.

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Authors and Affiliations

  1. Department of High-Risk Pregnancy and Perinatology, KIMS Health, 1, Vinod Nagar road, Anayara, Trivandrum, Kerala, 695029, India

    Brinda Sabu, Tazeen Khan & Vidyalekshmy R

  2. Department of Neonatology, KIMS Health, 1, Vinod Nagar road, Anayara, Trivandrum, Kerala, 695029, India

    Naveen Jain

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  1. Brinda Sabu
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  2. Tazeen Khan
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  3. Vidyalekshmy R
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  4. Naveen Jain
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All the authors have equally contributed to the article.

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Correspondence to Brinda Sabu.

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Sabu, B., Khan, T., R, V. et al. Congenital Intracranial Teratoma—An Intractable Enigma: A Case Report and Review of Literature. J. Fetal Med. 8, 231–235 (2021). https://doi.org/10.1007/s40556-021-00314-6

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  • DOI: https://doi.org/10.1007/s40556-021-00314-6

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