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
Angiofibrolipoma is a neoplasm composed of fibrocytes, capillaries and matured adipose tissues. It is a rare histopathologic variant of lipoma, characterized by matured adipocytes, blood vessels and dense collagenous tissues. It is an extremely rare tumor with very few cases reported in the literature. We are reporting a 9-year-old boy who presented with a right calf swelling noticed since birth, slowly increasing in size which became painful about a year prior to presentation (at about the age of 8 years). The mass extended from the popliteal fossa to the junction of the gastro-soleus. Mid calf circumference on the right was 44 cm and 24 cm on the left. Clinically there was no foot drop. He had neither preceding trauma nor fall. He had no systemic symptom. Pre-operative plain radiographs, incisional biopsy and other ancillary investigations were done. Histopathology result after excisional biopsy revealed angiofibrolipoma and postoperative clinical improvement was significant. To our knowledge, such a case has not been previously reported in the literature.
Download full-text PDF |
Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3804823 | PMC |
http://dx.doi.org/10.4081/rt.2013.e48 | DOI Listing |
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