Published online Mar 6, 2023. doi: 10.12998/wjcc.v11.i7.1642
Peer-review started: December 5, 2022
First decision: January 12, 2023
Revised: January 19, 2023
Accepted: February 16, 2023
Article in press: February 16, 2023
Published online: March 6, 2023
Processing time: 87 Days and 1 Hours
Extragonadal yolk sac tumors (YSTs) are rare, with only a low reported tumor occurrence outside the gonads locally and abroad. Extragonadal YSTs are usually a diagnostic challenge, because they are infrequent, but also because a thoughtful and detailed differential diagnostic process must be performed.
Here we present a case of an abdominal wall YST in a 20-year-old woman admitted with a tumor in the lower abdomen close to the umbilicus. The tumorectomy was performed. The histological examination revealed characteristic findings such as Schiller-Duval bodies, loose reticular structures, papillary structures, and eosinophilic globules. According to the immunohistochemical staining, the tumor tissue was positive for broad-spectrum cytokeratin, Spalt-like transcription factor 4, glypican-3, CD117, and epithelial membrane antigen. Based on the clinical information, histological features, and immunohistochemical staining profile, the tumor was diagnosed as a YST present in the abdominal wall.
Based on the clinical information, histological features, and immunohistochemical staining profile described above, the tumor was diagnosed as a primary YST in the abdominal wall.
Core Tip: Extragonadal yolk sac tumors (YSTs) are usually a diagnostic challenge, because they are infrequent, but also because a thoughtful and detailed differential diagnostic process must be performed. In this case, since the tumor presented classic yolk sac tumor features, and immunohistochemistry was concordant, the diagnostic process was more straightforward, but not simplistic. And this is the first reported case of a primary YST in the abdominal wall of an adult.