Published online Jul 26, 2019. doi: 10.12998/wjcc.v7.i14.1884
Peer-review started: March 15, 2019
First decision: April 18, 2019
Revised: May 3, 2019
Accepted: May 23, 2019
Article in press: May 23, 2019
Published online: July 26, 2019
Processing time: 136 Days and 18.3 Hours
Primary neuroendocrine tumors (NETs) in the presacral region are extremely rare, some of which are caused by other primary tumors or metastatic rectal carcinoids. Nevertheless, cases of NETs have been increasing in recent years. This report describes the first primary neuroendocrine tumor in the presacral region that was found at our hospital within the last five years.
The patient was identified as a 36-year-old woman with a presacral mass and pelvic floor pain. A digital rectal examination revealed a presacral mass with unclear margins and obvious tenderness. Magnetic resonance imaging (MRI) demonstrated a 57 mm × 29 mm presacral lump. An ultrasound-guided needle biopsy confirmed a well-differentiated neuroendocrine tumor. No other primary or metastatic tumors were found.
Comprehensive consideration of our case report and literature reported by others suggests that a conclusive diagnosis of NETs should be based on computed tomography/MRI and pathological examinations. The treatment of primary NETs in the presacral region mainly relies on surgical procedures with follow-up.
Core tip: This case highlights the need to include neoplastic diseases in the differential diagnosis of any potentially benign perianal abscess. A 36-year-old Asian woman was initially diagnosed with perianal abscess. Ultrasound-guided needle biopsy confirmed a well-differentiated neuroendocrine tumor, and then the patient underwent a sacrococcygeal tumor resection. A whole-body emission computed tomography scan was performed after the patient was discharged from the hospital, which revealed that she had no high expression of somatostatin receptors in the pleural cavity, abdominal cavity, or pelvis. There was no evidence of metastatic disease and no systemic symptoms or signs of carcinoid. These results confirmed that this was a primary presacral neuroendocrine tumor of level G2. The patient was advised to receive regular follow-up with her physician and magnetic resonance imaging.