Published online Oct 14, 2014. doi: 10.3748/wjg.v20.i38.14063
Revised: July 25, 2014
Accepted: September 12, 2014
Published online: October 14, 2014
Processing time: 149 Days and 0.2 Hours
Intramedullary spinal cord metastasis (ISCM) is very rare and its optimal treatment remains controversial. Pancreatic neuroendocrine tumor (pNET) is a rare tumor that usually presents with hepatic metastasis. Hepatic failure due to tumor progression is the major cause of death in cases of pNET. To date, no report has described a case of ISCM from pNET. Although spinal cord metastasis of a solid tumor is uncommon, it is a critical condition that can cause a potentially irreversible loss of neurologic function. Here, we report the case of a 45-year-old man who presented with leg weakness and voiding difficulty, and was found to have ISCM from pNET. Surgical treatment prevented further neurological deterioration. This is the first case report of ISCM from pNET.
Core tip: We report the first case of intramedullary spinal cord metastasis (ISCM) from a pancreatic neuroendocrine tumor. Despite its rarity, ISCM is a significant clinical condition that can cause critical neurologic issues. We suggest that taking an immediate surgical approach can increase the chances of restoring neurologic deficits and improving quality of life in cases of pancreatic neuroendocrine tumor with ISCM. Our report includes a review of previous studies of surgical and non-surgical approaches to ISCM.