Primary Gliosarcoma of the Cerebellum in a Young Pregnant Woman: Management Challenges and Immunohistochemical Features
Background. Gliosarcoma (GS) represents a rare, high-grade (WHO Grade IV), central nervous system neoplasm, characterized by a very poor prognosis. Similar to other high-grade gliomas, GS affects mainly adults in the 5th-7th decade of life and presents a higher incidence in males. The most reported...
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Series: | Case Reports in Surgery |
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doaj-e6544ee4eb044f71b0e6462c32b627fe2020-11-25T01:39:02ZengHindawi LimitedCase Reports in Surgery2090-69002090-69192019-01-01201910.1155/2019/71053617105361Primary Gliosarcoma of the Cerebellum in a Young Pregnant Woman: Management Challenges and Immunohistochemical FeaturesMarco Meloni0Salvatore Serra1Giulia Bellisano2Nikolaos Syrmos3Sanjeeva Jeyaretna4Mario Ganau5Department of Neurosurgery, San Francesco Hospital, Nuoro, ItalyDepartment of Neurosurgery, San Francesco Hospital, Nuoro, ItalyDepartment of Pathology, San Francesco Hospital, Nuoro, ItalyDepartment of Neurosurgery, Aristotle University of Thessaloniki, Macedonia, GreeceNuffield Division of Clinical Neurosciences and Department of Neurosurgery, Oxford University Hospitals, Oxford, UKNuffield Division of Clinical Neurosciences and Department of Neurosurgery, Oxford University Hospitals, Oxford, UKBackground. Gliosarcoma (GS) represents a rare, high-grade (WHO Grade IV), central nervous system neoplasm, characterized by a very poor prognosis. Similar to other high-grade gliomas, GS affects mainly adults in the 5th-7th decade of life and presents a higher incidence in males. The most reported locations of GS are the temporal lobe and the frontal lobe, while only eight cases of GS originating from the posterior cranial fossa are reported in the literature. Case Description. We report the first case occurring during pregnancy in a 33-year-old patient. Diagnosis was obtained on the 15th week of gestation when patient presented with signs and symptoms of life-threatening raised intracranial pressure. Surgical excision was followed by early recurrence and eventually disease progression because the patient refused adjuvant treatment to save her fetus. Conclusions. GS should be considered in the differential diagnosis of posterior cranial fossa tumors with radiological features of meningioma or glioblastoma, even in young patients. To this regard, sarcomas, solitary fibrous tumors, and even metastases should be considered, especially in light of the tendency of GS to give rise to extracranial localizations. Whenever an aggressive management with radical excision and adjuvant treatment is not safely achievable, disease progression is likely to be unavoidable.http://dx.doi.org/10.1155/2019/7105361 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Marco Meloni Salvatore Serra Giulia Bellisano Nikolaos Syrmos Sanjeeva Jeyaretna Mario Ganau |
spellingShingle |
Marco Meloni Salvatore Serra Giulia Bellisano Nikolaos Syrmos Sanjeeva Jeyaretna Mario Ganau Primary Gliosarcoma of the Cerebellum in a Young Pregnant Woman: Management Challenges and Immunohistochemical Features Case Reports in Surgery |
author_facet |
Marco Meloni Salvatore Serra Giulia Bellisano Nikolaos Syrmos Sanjeeva Jeyaretna Mario Ganau |
author_sort |
Marco Meloni |
title |
Primary Gliosarcoma of the Cerebellum in a Young Pregnant Woman: Management Challenges and Immunohistochemical Features |
title_short |
Primary Gliosarcoma of the Cerebellum in a Young Pregnant Woman: Management Challenges and Immunohistochemical Features |
title_full |
Primary Gliosarcoma of the Cerebellum in a Young Pregnant Woman: Management Challenges and Immunohistochemical Features |
title_fullStr |
Primary Gliosarcoma of the Cerebellum in a Young Pregnant Woman: Management Challenges and Immunohistochemical Features |
title_full_unstemmed |
Primary Gliosarcoma of the Cerebellum in a Young Pregnant Woman: Management Challenges and Immunohistochemical Features |
title_sort |
primary gliosarcoma of the cerebellum in a young pregnant woman: management challenges and immunohistochemical features |
publisher |
Hindawi Limited |
series |
Case Reports in Surgery |
issn |
2090-6900 2090-6919 |
publishDate |
2019-01-01 |
description |
Background. Gliosarcoma (GS) represents a rare, high-grade (WHO Grade IV), central nervous system neoplasm, characterized by a very poor prognosis. Similar to other high-grade gliomas, GS affects mainly adults in the 5th-7th decade of life and presents a higher incidence in males. The most reported locations of GS are the temporal lobe and the frontal lobe, while only eight cases of GS originating from the posterior cranial fossa are reported in the literature. Case Description. We report the first case occurring during pregnancy in a 33-year-old patient. Diagnosis was obtained on the 15th week of gestation when patient presented with signs and symptoms of life-threatening raised intracranial pressure. Surgical excision was followed by early recurrence and eventually disease progression because the patient refused adjuvant treatment to save her fetus. Conclusions. GS should be considered in the differential diagnosis of posterior cranial fossa tumors with radiological features of meningioma or glioblastoma, even in young patients. To this regard, sarcomas, solitary fibrous tumors, and even metastases should be considered, especially in light of the tendency of GS to give rise to extracranial localizations. Whenever an aggressive management with radical excision and adjuvant treatment is not safely achievable, disease progression is likely to be unavoidable. |
url |
http://dx.doi.org/10.1155/2019/7105361 |
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