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Multifocal primary intracranial yolk sac tumor in an adult patient: a case report and literature review
BACKGROUND: Yolk sac tumor is a type of germ cell tumor. It commonly arises in the gonads but sometimes can occur outside the gonads. Primary intracranial yolk sac tumors were very rare. It is always located in the pineal, suprasellar and posterior third ventricular region. The incidence of yolk sac...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9189240/ https://www.ncbi.nlm.nih.gov/pubmed/35706784 http://dx.doi.org/10.21037/tcr-21-2561 |
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author | Yang, Xiaochen Wang, Yubo Chen, Geng Hong, Xinyu |
author_facet | Yang, Xiaochen Wang, Yubo Chen, Geng Hong, Xinyu |
author_sort | Yang, Xiaochen |
collection | PubMed |
description | BACKGROUND: Yolk sac tumor is a type of germ cell tumor. It commonly arises in the gonads but sometimes can occur outside the gonads. Primary intracranial yolk sac tumors were very rare. It is always located in the pineal, suprasellar and posterior third ventricular region. The incidence of yolk sac tumor is estimated as less than 8% of all primary intracranial germ cell tumors. Multifocal primary intracranial yolk sac tumors have seldom been reported. CASE DESCRIPTION: Here we reported a 29 years old male patient with a sudden coma and a history of headaches for one month. Computed Tomography and magnetic resonance imaging of the head showed three masses located at the suprasellar region, pineal region and left temporal lobe separately. The mass at the left temporal lobe was successfully resected with emergency surgery, and decompressive craniectomy was also performed. Intraoperative findings revealed that the tumor was a solid mass with intra-tumoral haemorrhage. The pathology examination confirmed the diagnosis of yolk sac tumor. Hematoxylin and eosin staining clearly showed the Schiller-Duval body. Whole-brain radiotherapy was performed after the operation, and the patient died in a local hospital 11 months after the surgery. CONCLUSIONS: We reported a case of multifocal primary intracranial yolk sac tumor in an adult patient. Then we reviewed the literature and discussed the treatment and diagnosis of patients with primary intracranial yolk sac tumors. |
format | Online Article Text |
id | pubmed-9189240 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-91892402022-06-14 Multifocal primary intracranial yolk sac tumor in an adult patient: a case report and literature review Yang, Xiaochen Wang, Yubo Chen, Geng Hong, Xinyu Transl Cancer Res Case Report BACKGROUND: Yolk sac tumor is a type of germ cell tumor. It commonly arises in the gonads but sometimes can occur outside the gonads. Primary intracranial yolk sac tumors were very rare. It is always located in the pineal, suprasellar and posterior third ventricular region. The incidence of yolk sac tumor is estimated as less than 8% of all primary intracranial germ cell tumors. Multifocal primary intracranial yolk sac tumors have seldom been reported. CASE DESCRIPTION: Here we reported a 29 years old male patient with a sudden coma and a history of headaches for one month. Computed Tomography and magnetic resonance imaging of the head showed three masses located at the suprasellar region, pineal region and left temporal lobe separately. The mass at the left temporal lobe was successfully resected with emergency surgery, and decompressive craniectomy was also performed. Intraoperative findings revealed that the tumor was a solid mass with intra-tumoral haemorrhage. The pathology examination confirmed the diagnosis of yolk sac tumor. Hematoxylin and eosin staining clearly showed the Schiller-Duval body. Whole-brain radiotherapy was performed after the operation, and the patient died in a local hospital 11 months after the surgery. CONCLUSIONS: We reported a case of multifocal primary intracranial yolk sac tumor in an adult patient. Then we reviewed the literature and discussed the treatment and diagnosis of patients with primary intracranial yolk sac tumors. AME Publishing Company 2022-05 /pmc/articles/PMC9189240/ /pubmed/35706784 http://dx.doi.org/10.21037/tcr-21-2561 Text en 2022 Translational Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/. |
spellingShingle | Case Report Yang, Xiaochen Wang, Yubo Chen, Geng Hong, Xinyu Multifocal primary intracranial yolk sac tumor in an adult patient: a case report and literature review |
title | Multifocal primary intracranial yolk sac tumor in an adult patient: a case report and literature review |
title_full | Multifocal primary intracranial yolk sac tumor in an adult patient: a case report and literature review |
title_fullStr | Multifocal primary intracranial yolk sac tumor in an adult patient: a case report and literature review |
title_full_unstemmed | Multifocal primary intracranial yolk sac tumor in an adult patient: a case report and literature review |
title_short | Multifocal primary intracranial yolk sac tumor in an adult patient: a case report and literature review |
title_sort | multifocal primary intracranial yolk sac tumor in an adult patient: a case report and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9189240/ https://www.ncbi.nlm.nih.gov/pubmed/35706784 http://dx.doi.org/10.21037/tcr-21-2561 |
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