Severity: Warning
Message: file_get_contents(https://...@gmail.com&api_key=61f08fa0b96a73de8c900d749fcb997acc09&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 197
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 197
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 271
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3165
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 597
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 511
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 317
Function: require_once
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Background: Solitary fibrous tumors are rare central nervous system neoplasms with high rates of local recurrence and distant metastasis. To date, no instances of metastatic dissemination from the spine to the ventricle with malignant progression have been documented.
Case Presentation: A 32-year-old male patient of Chinese ethnicity was diagnosed with a grade 2 intraspinal solitary fibrous tumor, demonstrating metastatic spread to the trigone region of the lateral ventricle. Despite cystic degeneration, the solid component of the metastatic lesion exhibited signal intensity similar to that of the primary tumor on imaging. A piecemeal gross total resection was achieved, and postoperative immunohistochemical analysis confirmed that the metastatic lesion was categorized as grade 3, with an increase in the Ki-67 proliferation index from 20% to 30%. Both the primary and metastatic tumors exhibited negative expression of CD34. Although radiotherapy was considered, consensus on its use was not reached, and the patient succumbed to tumor progression 17 months later.
Conclusion: This case underscores the importance of recognizing the potential for malignant transformation and intracranial metastasis in intraspinal solitary fibrous tumors, highlighting the need for vigilant monitoring and possible aggressive treatment strategies.
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Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12398998 | PMC |
http://dx.doi.org/10.1186/s13256-025-05518-2 | DOI Listing |