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Fetal Ganglioneuroblastoma: A Rare Entity with Antenatal Diagnosis and Postnatal Follow Up
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AbstractFetal abdominal masses can be challenging to counsel due to uncertain diagnosis and outcomes. We report a case of a midline upper retroperitoneal mass found incidentally during a routine third trimester ultrasound. Despite not being a suprarenal mass, ultrasound and magnetic resonance imaging indicated neuroblastoma prenatally. With the generally favorable prognosis for prenatally diagnosed neuroblastomas, expectant counseling was given. Postnatal imaging and biopsy confirmed ganglioneuroblastoma, a rare subtype. A conservative approach was taken, and after initial growth, the mass spontaneously regressed 5 months after birth, nearly resolving by 8 months.
Georg Thieme Verlag KG
Title: Fetal Ganglioneuroblastoma: A Rare Entity with Antenatal Diagnosis and Postnatal Follow Up
Description:
AbstractFetal abdominal masses can be challenging to counsel due to uncertain diagnosis and outcomes.
We report a case of a midline upper retroperitoneal mass found incidentally during a routine third trimester ultrasound.
Despite not being a suprarenal mass, ultrasound and magnetic resonance imaging indicated neuroblastoma prenatally.
With the generally favorable prognosis for prenatally diagnosed neuroblastomas, expectant counseling was given.
Postnatal imaging and biopsy confirmed ganglioneuroblastoma, a rare subtype.
A conservative approach was taken, and after initial growth, the mass spontaneously regressed 5 months after birth, nearly resolving by 8 months.
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