Primary carcinoid tumors of the liver

Gary Schwartz, Agnes Colanta, Harold Gaetz, John Olichney, Fadi Attiyeh

Research output: Contribution to journalArticlepeer-review

22 Scopus citations


Background: 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.

Original languageEnglish (US)
Article number91
JournalWorld Journal of Surgical Oncology
StatePublished - Aug 27 2008
Externally publishedYes

ASJC Scopus subject areas

  • Surgery
  • Oncology


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