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lüll Primary carcinoid tumors of the liver Schwartz G; Colanta A; Gaetz H; Olichney J; Attiyeh FWorld J Surg Oncol 2008[Aug]; 6 (ä): 91BACKGROUND: Primary carcinoid tumors of the liver are uncommon and rarely symptomatic. The diagnosis of primary hepatic etiology requires rigorous workup and continued surveillance to exclude a missed primary. CASE PRESENTATION: We present a case of a 62-year-old female with a primary hepatic carcinoid tumor successfully resected, now with three years of disease-free follow-up. We present a review of the current literature regarding the diagnosis, pathology, management, and natural history of this disease entity. CONCLUSION: Primary carcinoid tumors of the liver are rare, therefore classifying their nature as primary hepatic in nature requires extensive workup and prolonged follow-up. All neuroendocrine tumors have an inherent malignant potential that must be recognized. Management remains surgical resection, with several alternative options available for non-resectable tumors and severe symptoms. The risk of recurrence of primary hepatic carcinoid tumors after resection remains unknown.|Carcinoid Tumor/*diagnosis/*surgery[MESH]|Female[MESH]|Humans[MESH]|Liver Neoplasms/*diagnosis/*surgery[MESH]|Middle Aged[MESH] |