Severity: Warning
Message: file_get_contents(https://...@gmail.com&api_key=61f08fa0b96a73de8c900d749fcb997acc09&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
Syringocystadenoma papilliferum is a rare, hamartomatous benign tumor originating from either the eccrine or apocrine sweat glands. We report a case of a 30-year-old female who presented with a 10-year history of an asymptomatic, slow-growing scalp lesion following head trauma. A scalp examination revealed a single, rounded 3 mm fleshy erythematous nodule with a central crust in the right parietal area. a biopsy revealed downward papillomatous extensions in the epidermis and multiple epithelial sheets with dilated ducts lined by columnar cells in the dermis. A diagnosis of syringocystadenoma papilliferum was confirmed based on these clinicopathological findings. The patient was reassured and underwent complete surgical excision of the lesion.
Download full-text PDF |
Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11461806 | PMC |
http://dx.doi.org/10.7759/cureus.68960 | DOI Listing |
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