Intracranial bifocal germinoma.
Bifocal germinoma
Epiphysis intracranial germ cell tumour
Hypophysis
Pineal tumor
Suprasellar tumor
Journal
Radiology case reports
ISSN: 1930-0433
Titre abrégé: Radiol Case Rep
Pays: Netherlands
ID NLM: 101467888
Informations de publication
Date de publication:
Sep 2022
Sep 2022
Historique:
received:
07
05
2022
revised:
25
05
2022
accepted:
28
05
2022
entrez:
27
6
2022
pubmed:
28
6
2022
medline:
28
6
2022
Statut:
epublish
Résumé
Primary intracranial germ cell tumors are rare, often affecting children and young patients. Germinomas are the most common type of germ cell tumors. We present the case of a 10-year-old child, who was admitted with decreased visual acuity, asthenia, polyuro-polydipsic syndrome, and gait disorder. His biological assessment showed an hypocortisolemia and diabetes insipidus. Imaging found a bifocal process in the suprasellar and pineal region, suggestive of a bifocal germinoma. Imaging data and the positivity of human chorionic gonadotrophin in the cerebrospinal fluid were in favor of the diagnosis of bifocal germinal tumor confirmed by biopsy. Currently the patient is hospitalized in pediatric oncology department. The diagnosis of germ cell tumors is based on imaging, tumor marker assays, and biopsy. They are treated by radiation therapy alone or in combination with reduction chemotherapy, and surgery for tumor residues. The location of the tumor usually makes surgery difficult.
Identifiants
pubmed: 35755113
doi: 10.1016/j.radcr.2022.05.080
pii: S1930-0433(22)00435-6
pmc: PMC9214722
doi:
Types de publication
Case Reports
Langues
eng
Pagination
3015-3018Informations de copyright
© 2022 The Authors. Published by Elsevier Inc. on behalf of University of Washington.
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