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: 1034
Function: getPubMedXML
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3152
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
Extramedullary plsmocytoma (plasmocytic lymphoma) is very rare, it seems to have an indolent course and the progression to a multiple myeloma is very rare (about 30 cases are reported in the literature). We report the case of 68-old-woman who presented in 1997 with an axillary left node. Physical examination, biologic and radiologic tests were normal. The histologic examination (of this mass) revealed a primary extramedullary plasmocytoma. She was treated with the combination of chemiotherapy and radiotherapy. 18 months later, at the follow up, the patient developed an Ig A lambda multiple myeloma. She was treated by chemiotherapy with favorable course.
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