Case Reports
Vol. 16 (2021)
https://doi.org/10.3269/1970-5492.2021.16.23
CONGENITAL NEUROBLASTOMA: A RARE CASE OF PLURIVISCERAL METASTATIC DISSEMINATION
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All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
Received: October 14 2025
Published: October 15 2025
Published: October 15 2025
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Neuroblastoma is one of the most common neonatal tumors. It involves children in early infancy
and originates from neural crest cells of the adrenal gland medulla or sympathetic glia. We report
an unusual case of congenital poorly differentiated neuroblastoma with multiple metastases in the
brain and cerebellum. The biophysical profile showed a prominent polyhydramnios at 25.3 weeks
of gestation; meantime, the mother was diagnosed with gestational diabetes. The mass was detected
during the third ultrasonographic examination at 31.4 weeks of gestation. The fetus lived only one
day after birth and the postmortem examinations were performed subsequently. An autopsy was
performed both to understand the causes of death and to identify any profiles of professional
responsibility. The histological examination confirmed the diagnosis: a neoplasm arising from the
lower right limb and pelvis.
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How to Cite
CONGENITAL NEUROBLASTOMA: A RARE CASE OF PLURIVISCERAL METASTATIC DISSEMINATION. (2025). EuroMediterranean Biomedical Journal, 16. https://doi.org/10.3269/1970-5492.2021.16.23
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