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: 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: 1057
Function: getPubMedXML
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3175
Function: GetPubMedArticleOutput_2016
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
Inflammatory myofibroblastic tumor (IMT) is an uncommon neoplasm that predominantly affects soft tissues and viscera. This abstract presents a unique case of IMT arising from the gingiva of a 32-year-old male. IMT is characterized by its variable clinical and clinic-histopathological presentation, often mimicking other malignancies, which can lead to diagnostic challenges. While IMT is generally considered benign, its potential for local recurrence and rare malignant transformation brings our attention to the importance of long-term follow-up. This case highlights the need for heightened clinical awareness of IMT as a differential diagnosis for intraoral masses in children and young adults.
Download full-text PDF |
Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11890678 | PMC |
http://dx.doi.org/10.1007/s12070-024-05187-5 | DOI Listing |
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