Pleomorphic xanthoastrocytoma at the pineal region: rare case report with successful surgical management

Abstract Background Pineal region tumors are commonly present in the pediatric age group. However, pleomorphic xanthoastrocytoma (PXA) is very rare at this region, and only few case reports have been reported till now in literature. Case presentation Here, we report a rare case of pineal region, jux...

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Main Authors: Saraj Kumar Singh, Krishan Kumar Sharma, Tarun Kumar
Format: Article
Language:English
Published: SpringerOpen 2021-07-01
Series:Egyptian Journal of Neurosurgery
Subjects:
Online Access:https://doi.org/10.1186/s41984-021-00107-z
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spelling doaj-17ce6e5c8fb14583b5dde0a5e111b31c2021-07-18T11:36:49ZengSpringerOpenEgyptian Journal of Neurosurgery2520-82252021-07-013611610.1186/s41984-021-00107-zPleomorphic xanthoastrocytoma at the pineal region: rare case report with successful surgical managementSaraj Kumar Singh0Krishan Kumar Sharma1Tarun Kumar2Department of Neurosurgery, AIIMS PatnaDepartment of Neurosurgery, AIIMS PatnaDepartment of Pathology, AIIMS PatnaAbstract Background Pineal region tumors are commonly present in the pediatric age group. However, pleomorphic xanthoastrocytoma (PXA) is very rare at this region, and only few case reports have been reported till now in literature. Case presentation Here, we report a rare case of pineal region, juxta-thalamic, pleomorphic xanthoastrocytoma (PXA) in an 11-year-old male child. The child presented with severe headache after which MRI was done. It was suggestive of pineal region low-grade tumor. The patient was operated in Parkbench position with SCIT (supracerebellar approach) in a retractor-free manner. Gross total resection was done. However, the patient developed postoperative left-sided hemiparesis. It got improved in 1 month, and the patient became ambulatory. Histopathology came out as pleomorphic xanthoastrocytoma. Conclusion Surgical management should include careful resection near the internal capsule to avoid postoperative hemiparesis. Also, shunt should be delayed in the cystic cavity created by resection of tumor.https://doi.org/10.1186/s41984-021-00107-zPleomorphic xanthoastrocytomaPineal regionThalamusSupracerebellar infratentorial
collection DOAJ
language English
format Article
sources DOAJ
author Saraj Kumar Singh
Krishan Kumar Sharma
Tarun Kumar
spellingShingle Saraj Kumar Singh
Krishan Kumar Sharma
Tarun Kumar
Pleomorphic xanthoastrocytoma at the pineal region: rare case report with successful surgical management
Egyptian Journal of Neurosurgery
Pleomorphic xanthoastrocytoma
Pineal region
Thalamus
Supracerebellar infratentorial
author_facet Saraj Kumar Singh
Krishan Kumar Sharma
Tarun Kumar
author_sort Saraj Kumar Singh
title Pleomorphic xanthoastrocytoma at the pineal region: rare case report with successful surgical management
title_short Pleomorphic xanthoastrocytoma at the pineal region: rare case report with successful surgical management
title_full Pleomorphic xanthoastrocytoma at the pineal region: rare case report with successful surgical management
title_fullStr Pleomorphic xanthoastrocytoma at the pineal region: rare case report with successful surgical management
title_full_unstemmed Pleomorphic xanthoastrocytoma at the pineal region: rare case report with successful surgical management
title_sort pleomorphic xanthoastrocytoma at the pineal region: rare case report with successful surgical management
publisher SpringerOpen
series Egyptian Journal of Neurosurgery
issn 2520-8225
publishDate 2021-07-01
description Abstract Background Pineal region tumors are commonly present in the pediatric age group. However, pleomorphic xanthoastrocytoma (PXA) is very rare at this region, and only few case reports have been reported till now in literature. Case presentation Here, we report a rare case of pineal region, juxta-thalamic, pleomorphic xanthoastrocytoma (PXA) in an 11-year-old male child. The child presented with severe headache after which MRI was done. It was suggestive of pineal region low-grade tumor. The patient was operated in Parkbench position with SCIT (supracerebellar approach) in a retractor-free manner. Gross total resection was done. However, the patient developed postoperative left-sided hemiparesis. It got improved in 1 month, and the patient became ambulatory. Histopathology came out as pleomorphic xanthoastrocytoma. Conclusion Surgical management should include careful resection near the internal capsule to avoid postoperative hemiparesis. Also, shunt should be delayed in the cystic cavity created by resection of tumor.
topic Pleomorphic xanthoastrocytoma
Pineal region
Thalamus
Supracerebellar infratentorial
url https://doi.org/10.1186/s41984-021-00107-z
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AT krishankumarsharma pleomorphicxanthoastrocytomaatthepinealregionrarecasereportwithsuccessfulsurgicalmanagement
AT tarunkumar pleomorphicxanthoastrocytomaatthepinealregionrarecasereportwithsuccessfulsurgicalmanagement
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