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
Systemic lupus erythematosus (SLE) is an autoimmune disease that affects multiple organs, and its coexistence with Giant Cell Arteritis (GCA) is extremely rare. We present, to our knowledge, the first reported case of a 56-year-old woman with SLE and extracranial GCA who presented with chest pain as the cardinal symptom. The diagnosis was subsequently confirmed by imaging studies, ruling out Takayasu arteritis and SLE-related vasculitis. She required treatment with glucocorticoids and tocilizumab, showing a satisfactory evolution. Accurate diagnosis was key to preventing serious vascular complications and achieving favorable clinical recovery.
Download full-text PDF |
Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11567006 | PMC |
http://dx.doi.org/10.7759/cureus.71634 | DOI Listing |
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