Open Access
J Neurol Surg Rep 2016; 77(03): e118-e120
DOI: 10.1055/s-0036-1586211
Case Report
Georg Thieme Verlag KG Stuttgart · New York

Management of Giant Cervical Teratoma with Intracranial Extension Diagnosed in Utero

Authors

  • Jayesh P. Thawani

    1   Department of Neurosurgery, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, United States
  • Michael J. Randazzo

    2   Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States
  • Nickpreet Singh

    2   Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States
  • Jared M. Pisapia

    1   Department of Neurosurgery, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, United States
  • Kalil G. Abdullah

    1   Department of Neurosurgery, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, United States
  • Phillip B. Storm

    1   Department of Neurosurgery, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, United States
    3   Division of Neurosurgery, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States
    4   The Center for Fetal Diagnosis and Treatment, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States
Further Information

Publication History

05 May 2016

19 June 2016

Publication Date:
26 July 2016 (online)

Abstract

Cervical teratomas are rare germ cell tumors affecting the fetus that are associated with significant morbidity and mortality due to an increased risk of airway obstruction at delivery. These tumors can commonly produce polyhydramnios that results from the fetus' impaired ability to swallow amniotic fluid. Improved rates of prenatal diagnosis through comprehensive evaluations and imaging have dramatically impacted the perinatal management of infants with this condition. Here, we report a patient diagnosed with polyhydramnios whose fetus was discovered to have a giant cervical teratoma on imaging studies. The child underwent surgical resection after having the airway secured under the uteroplacental support as part of an ex utero intrapartum treatment procedure performed at 37 weeks. The following gross pathological and magnetic resonance images demonstrate this condition and its currently accepted treatment.

Funding

None.