Fetal Ganglioneuroblastoma: A Rare Entity with Antenatal Diagnosis and Postnatal Follow Up
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.
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
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Englisch
- Bibliographic citation
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Fetal Ganglioneuroblastoma: A Rare Entity with Antenatal Diagnosis and Postnatal Follow Up ; day:16 ; month:08 ; year:2024
Journal of fetal medicine ; (16.08.2024)
- Contributor
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Varshney, Alok
Kapoor, Aakriti
Kaur, Shina
Kapoor, Tushar
Kapoor, Aakaar
Kapoor, Apurva
Kapoor, Ravi
- DOI
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10.1055/s-0044-1788925
- URN
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urn:nbn:de:101:1-2410031042104.549726790422
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:27 AM CEST
Data provider
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Varshney, Alok
- Kapoor, Aakriti
- Kaur, Shina
- Kapoor, Tushar
- Kapoor, Aakaar
- Kapoor, Apurva
- Kapoor, Ravi
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