| Literature DB >> 35365470 |
Orlando De Jesus1, Joel E Pellot Cestero2, Frances M Gómez-González3, Román Vélez3.
Abstract
Choriocarcinoma is a highly malignant tumour emerging from the syncytiotrophoblast divided into gestational and non-gestational presentations. Primary choriocarcinoma of the mediastinum is rare. Metastases to the brain often occur; however, brainstem involvement has not been reported for non-gestational choriocarcinoma. We described a middle-aged man who developed a complete left oculomotor nerve paralysis secondary to a brainstem tumour at the midbrain. The workup for the primary source of the brainstem tumour included a chest CT scan, which revealed a mediastinal mass. A mediastinal mass needle biopsy confirmed the diagnosis of primary mediastinal choriocarcinoma. Despite aggressive chemotherapy, the patient died 6 months after the initial presentation from neurological complications and multiorgan failure. © BMJ Publishing Group Limited 2022. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: Brain stem / cerebellum; Neuroimaging; Neurooncology; Neurosurgery; Pathology
Mesh:
Year: 2022 PMID: 35365470 PMCID: PMC8977749 DOI: 10.1136/bcr-2021-248389
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X