Synchronous congenital malignant rhabdoid tumor of the orbit and cerebellar atypical teratoid/rhabdoid tumor: Case report.
CT
MRI
MRT
Orbit
Journal
Radiology case reports
ISSN: 1930-0433
Titre abrégé: Radiol Case Rep
Pays: Netherlands
ID NLM: 101467888
Informations de publication
Date de publication:
Nov 2023
Nov 2023
Historique:
received:
02
07
2023
revised:
25
07
2023
accepted:
29
07
2023
medline:
8
9
2023
pubmed:
8
9
2023
entrez:
8
9
2023
Statut:
epublish
Résumé
Malignant rhabdoid tumor is an uncommon pediatric tumor that often arises from the kidneys but can also develop in other soft tissues including the orbits, where it is known as atypical teratoid rhabdoid tumor. Orbital location is exceptional, with just a few reported cases. Imaging allows for an accurate diagnosis, but histological confirmation is required. The treatment is yet unclear but nearly often surgical, either with or without chemotherapy. In this report, we present a case of a neonate of 1-month-old with an orbital primary malignant rhabdoid tumor with synchronous cerebellar location. The patient was unable to undergo surgery, he had chemotherapy, and unfortunately died 1 week after following palliative treatment. We will illustrate this clinical experience and point out the importance of radiological imaging in the assessment of this uncommon condition.
Identifiants
pubmed: 37680666
doi: 10.1016/j.radcr.2023.07.074
pii: S1930-0433(23)00513-7
pmc: PMC10480453
doi:
Types de publication
Case Reports
Langues
eng
Pagination
3979-3983Informations de copyright
© 2023 The Authors. Published by Elsevier Inc. on behalf of University of Washington.
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