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Giant Hepatic Carcinoid: A Rare Tumor with a Favorable Prognosis

DOI: 10.1155/2014/456509

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Abstract:

Primary hepatic carcinoids are rare tumors that are often diagnosed at a locally advanced stage. Their primary nature can only be ascertained after thorough investigations and long-term follow-up to exclude another primary origin. As with secondary neuroendocrine liver tumors, surgical resection remains the mainstay of therapy. Despite their large size and often central location liver resection is often feasible, offering long-term survival and cure to most patients. In selected patients liver transplantation appears to be a good indication for tumors not amenable to liver resection. An aggressive surgical attitude is therefore warranted. We report a large and unusually fast-growing liver carcinoid that appeared only marginally resectable in a patient who remains free of disease four years after surgery. 1. Introduction With less than 100 reports in the literature little is known of primary hepatic carcinoids. They often present as large centrally situated liver masses, characteristics that may discourage attempts at resection. Data is scarce on the outcome of surgical treatment but these tumors seem to be associated with a favorable prognosis, justifying an aggressive surgical approach. Presented here is a patient with a giant primary liver carcinoid that appeared only marginally resectable, who remains disease free four years after surgical resection. 2. Case Report A 52-year-old female complained of fatigue and intermittent fever of one-year duration. There was no history of liver failure, hematemesis, flushing, or diarrhea. She had undergone a previous appendectomy. Abdominal ultrasound revealed a heterogeneous 8?cm right lobe focal liver lesion. Contrast enhanced CT performed one month later showed a solid 15?cm liver mass with a hypodense core that was suggestive of an atypical hemangioma. The patient came to our attention two months after the initial ultrasound with palpable hepatomegaly. MR showed a hypervascularized solitary liver lesion measuring 20?cm (Figure 1). Malignancy was further suspected by FDG-PET scan showing increased uptake. Laboratory data showed normal liver function and hepatitis B and C serologies were negative. Serum tumor markers including CEA, AFP, CA 12.5, CA 19.9, and NSE were within normal range while chromogranin A was moderately elevated. 24-hour urinary 5-HIAA excretion was normal. Chest CT showed no signs of malignancy. No primary tumor was found at gastroscopy and colonoscopy. Laparoscopy showed that the right liver lobe was completely occupied by a polylobulated firm white mass. The left lobe appeared healthy and

References

[1]  M. A. Maggard, J. B. O'Connell, and C. Y. Ko, “Updated population-based review of carcinoid tumors,” Annals of Surgery, vol. 240, no. 1, pp. 117–122, 2004.
[2]  I. M. Modlin and A. Sandor, “An analysis of 8305 cases of carcinoid tumours,” Cancer, vol. 79, no. 4, pp. 813–829, 1997.
[3]  C.-W. Lin, C.-H. Lai, C.-C. Hsu et al., “Primary hepatic carcinoid tumor: a case report and review of the literature,” Cases Journal, vol. 2, no. 1, article 90, 2009.
[4]  Y.-Q. Huang, F. Xu, J.-M. Yang, and B. Huang, “Primary hepatic neuroendocrine carcinoma: clinical analysis of 11 cases,” Hepatobiliary and Pancreatic Diseases International, vol. 9, no. 1, pp. 44–48, 2010.
[5]  S. W. Fenwick, J. I. Wyatt, G. J. Toogood, and J. P. A. Lodge, “Hepatic resection and transplantation for primary carcinoid tumors of the liver,” Annals of Surgery, vol. 239, no. 2, pp. 210–219, 2004.
[6]  G. Gravante, N. de Liguori Carino, J. Overton, T. M. Manzia, and G. Orlando, “Primary carcinoids of the liver: a review of symptoms, diagnosis and treatments,” Digestive Surgery, vol. 25, no. 5, pp. 364–368, 2008.
[7]  P. Kongkam, M. Al-Haddad, S. Attasaranya et al., “EUS and clinical characteristics of cystic pancreatic neuroendocrine tumors,” Endoscopy, vol. 40, no. 7, pp. 602–605, 2008.
[8]  H. Cerwenka, “Neuroendocrine liver metastases: contributions of endoscopy and surgery to primary tumor search,” World Journal of Gastroenterology, vol. 18, no. 10, pp. 1009–1014, 2012.
[9]  J. A. Norton, R. S. Warren, M. G. Kelly et al., “Aggressive surgery for metastatic liver neuroendocrine tumors,” Surgery, vol. 134, no. 6, pp. 1057–1065, 2003.
[10]  E. S. Glazer, J. F. Tseng, W. Al-Refaie et al., “Long-term survival after surgical management of neuroendocrine hepatic metastases,” HPB, vol. 12, no. 6, pp. 427–433, 2010.
[11]  J. M. Sarmiento, F. G. Que, C. S. Grant et al., “Concurrent resections of pancreatic islet cell cancers with synchronous hepatic metastases: outcomes of an aggressive approach,” Surgery, vol. 132, no. 6, pp. 976–983, 2002.
[12]  R. S. Chamberlain, D. Canes, K. T. Brown et al., “Hepatic neuroendocrine metastases: does intervention alter outcomes?” Journal of the American College of Surgeons, vol. 190, no. 4, pp. 432–445, 2000.
[13]  S. Scigliano, R. Lebtahi, F. Maire et al., “Clinical and imaging follow-up after exhaustive liver resection of endocrine metastases: a 15-year monocentric experience,” Endocrine-Related Cancer, vol. 16, no. 3, pp. 977–990, 2009.
[14]  J. M. Sarmiento, G. Heywood, J. Rubin, D. M. Ilstrup, D. M. Nagorney, and F. G. Que, “Surgical treatment of neuroendocrine metastases to the liver: a plea for resection to increase survival,” Journal of the American College of Surgeons, vol. 197, no. 1, pp. 29–37, 2003.
[15]  J. Rosenau, M. J. Bahr, R. Von Wasielewski et al., “Ki67, e-cadherin, and p53 as prognostic indicators of long-term outcome after liver transplantation for metastatic neuroendocrine tumors,” Transplantation, vol. 73, no. 3, pp. 386–394, 2002.
[16]  Y. P. Le Treut, J. R. Delpero, B. Dousset et al., “Results of liver transplantation in the treatment of metastatic neuroendocrine tumors: a 31-case French multicentric report,” Annals of Surgery, vol. 225, no. 4, pp. 355–364, 1997.
[17]  R. Gedaly, M. F. Daily, D. Davenport et al., “Liver transplantation for the treatment of liver metastases from neuroendocrine tumors: an analysis of the UNOS database,” Archives of Surgery, vol. 146, no. 8, pp. 953–958, 2011.
[18]  Y. Mizuno, N. Ohkohchi, K. Fujimori et al., “Primary hepatic carcinoid tumor: a case report,” Hepato-Gastroenterology, vol. 47, no. 32, pp. 528–530, 2000.
[19]  C. D. Knox, C. D. Anderson, L. W. Lamps, R. B. Adkins, and C. W. Pinson, “Long-term survival after resection for primary hepatic carcinoid tumor,” Annals of Surgical Oncology, vol. 10, no. 10, pp. 1171–1175, 2003.
[20]  N. de Liguori Carino, T. M. Manzia, L. Tariciotti, M. Berlanda, G. Orlando, and G. Tisone, “Liver transplantation in primary hepatic carcinoid tumor: case report and literature review,” Transplantation Proceedings, vol. 41, no. 4, pp. 1386–1389, 2009.
[21]  D. Alekseev, A. Goralczyk, T. Lorf, G. Ramadori, and A. Obed, “Ten years survival with excellent outcome after living donor liver transplantation from 70 years old donor for primary hepatic neuroendocrine carcinoma: case report,” International Journal of Surgery Case Reports, vol. 3, no. 1, pp. 34–36, 2012.
[22]  J. C. Arnold, J. G. O'Grady, G. L. Bird, R. Y. Calne, and R. Williams, “Liver transplantation for primary and secondary hepatic apudomas,” British Journal of Surgery, vol. 76, no. 3, pp. 248–249, 1989.
[23]  S. Andreola, L. Lombardi, R. A. Audisio et al., “A clinicopathologic study of primary hepatic carcinoid tumors,” Cancer, vol. 65, no. 5, pp. 1211–1218, 1990.
[24]  S. C. Krishnamurthy, V. Dutta, S. A. Pai, et al., “Primary carcinoid tumor of the liver: report of four resected cases including one with gastrin production,” Journal of Surgical Oncology, vol. 62, no. 3, pp. 218–221, 1996.
[25]  B. W?ngberg, O. Nllsson, V. Johanson et al., “Somatostatin receptors in the diagnosis and therapy of neuroendocrine tumors,” Oncologist, vol. 2, no. 1, pp. 50–58, 1997.
[26]  A. Otte, J. Mueller-Brand, S. Dellas, E. U. Nitzsche, R. Herrmann, and H. R. Maecke, “Yttrium-90-labelled somatostatin-analogue for cancer treatment,” The Lancet, vol. 351, no. 9100, pp. 417–418, 1998.

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