Severity: Warning
Message: file_get_contents(https://...@pubfacts.com&api_key=b8daa3ad693db53b1410957c26c9a51b4908&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 176
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 176
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 250
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3122
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 316
Function: require_once
Supratentorial cortical ependymoma is an extremely rare malignancy in the pediatric population, especially in very young age groups. Most of the reported cases present with dramatic neurological symptoms like seizures and sudden onset hemiplegia. We hereby report a case of anaplastic supra-cortical ependymoma in a 13-month-old male child, with subtle seizures for four weeks. The child, who was brought for non-neurological complaints to the outpatient clinic, was found to have abnormal staring episodes. An electroencephalogram showed focal epilepsy and an MRI brain showed a large intra-axial lesion in the left frontal area. The child underwent gross total resection of the lesion and histopathology revealed WHO grade 3 cortical ependymoma.
Download full-text PDF |
Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10183097 | PMC |
http://dx.doi.org/10.7759/cureus.37555 | DOI Listing |
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