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Fetal Ganglioneuroblastoma: A Rare Entity with Antenatal Diagnosis and Postnatal Follow Up

Year: 2024
Type: article
Study design: Case Report
Abstract: Fetal 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.
Language: English
Subfield: Neurology
Field: Medicine
Open Access status: hybrid
Estimated APC paid: $3,390
OpenAlex ID: W4401629809
FWCI:
Cites: 10
Cited by:
Related to: 10