J Korean Surg Soc.
2000 May;58(5):650-655.
Clinicopathologic Characteristics of Neuroendocrine Tumor of the Stomach
- Affiliations
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- 1Department of Surgery Gastrointestinal division, University of Ulsan, College of Medicine and Asan Medical Center, Seoul, Korea.
- 2Department of Pathology, University of Ulsan, College of Medicine and Asan Medical Center, Seoul, Korea.
Abstract
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PURPOSE: Very few cases of neuroendocrine tumor of the stomach have been reported in Korea. The
prognosis of gastric neuroendocrine tumors is known to be poorer than that of ordinary gastric
carcinomas. The purpose of this retrospective study was to review the clinicopathologic features of seven
cases of this unusual gastric tumor. METHODS: Excluding the tumor containing only sparse neuroendocrine
differentiation, we resected 7 typical neuroendocrine tumors from January 1995 to December 1997 at
Asan Medical Center; 2,346 gastric cancer patients were treated surgically during the same period.
Average follow up period was 22.6 months. RESULTS: A typical well demarcated tumor margin was
observed in four of the seven cases. The entire tumor was located on the distal stomach. Even when
the tumor had deep ulcerations, the tumor cells had not infiltrated the serosal layer. Three cases showed
recurrence of disease. All the recurrences were found in the liver within 12 months, and two of them,
who were not indicated for chemotherapy, died within 10 months after diagnosis of recurrence. One
patient with a recurrence was treated with systemic chemotherapy just after the diagnosis and was still
alive after 29 months. CONCLUSION: Gastric neuroendocrine tumor frequently recurs the liver even in an
early stage and especially when preoperative CEA is increased. We experienced a case of successful
control of hepatic metastasis by using systemic chemotherapy.