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
Ischemic fasciitis (IF) is a rare pseudosarcomatous lesion usually occurring in physically debilitated or immobilized, elderly patients. The current case presents a 76-year-old mobile man with IF on his back. The 33-mm subcutaneous lesion, focally involving the latissimus dorsi muscle, had been slowly increasing in size for 2 months and was clinically suggested to be a soft-tissue sarcoma. The fragmented biopsy specimens showed a chiefly scattered proliferation of spindle or stellate cells with plump nuclei within myxofibrous stroma. Zonation was not evident, but the lesion contained fibrinous deposits. These findings indicated a possible diagnosis of IF. The lesion spontaneously disappeared 5 months after the biopsy. The presence of fibrin-like deposits within myxofibrous stroma could be a hallmark for the correct diagnosis of IF.
Download full-text PDF |
Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11443586 | PMC |
http://dx.doi.org/10.3892/etm.2024.12724 | DOI Listing |
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