Appendiceal mixed adenoneuroendocrine carcinomas, a rare entity that can present as a Krukenberg tumor: case report and review of the literature

作者：Romeo Margarita^*; Quer Ariadna; Tarrats Antoni; Molina Carlos; Radua Joaquim; Manzano Jose Luis

来源：World Journal of Surgical Oncology, 2015, 13(1): 325.

DOI：10.1186/s12957-015-0740-1

• Goblet cell carcinoid
• Adenoneuroendocrine carcinoma
• Appendix
• Adenocarcinoid
• Krukenberg tumor

Background: Mixed adenoneuroendocrine carcinoma is a rare tumor recently recognized as a new category in the last World Health Organization (WHO) classification of appendiceal tumors (2010). This term has been proposed to designate carcinomas of the appendix that arise by progression from a pre-existing goblet cell carcinoid. Mixed adenoneuroendocrine carcinomas are more aggressive tumors than typical goblet cell carcinoids and usually present with peritoneal spreading and ovarian masses. Staging, some histological features, and completeness of surgery are factors that determine its evolution.
Case Presentation: We report the case of a mixed adenoneuroendocrine carcinoma-signet ring cell subtype-that presented as a Krukenberg tumor of unknown primary.
Conclusion: The review of literature is focused on the most recent WHO pathologic classification of appendiceal tumors containing goblet cell clusters, which seems to correlate with prognosis. A management proposal for mixed adenoneuroendocrine carcinomas reported in previous literature is also discussed. This ranges from right hemicolectomy to cytoreduction plus hyperthermic intraperitoneal chemotherapy, in both cases usually followed by intravenous chemotherapy.

• 出版日期2015-11-26