Hepatic pseudocystic metastasis of well-differentiated ileal neuroendocrine tumor: a case report with review of the literature

[1] Estermann F(1996)Pseudocystic metastases of carcinoma of the uterine cervix mimicking polycystic liver disease Gastroenterol Clin Biol 12 1125-1128

[2] Thiebault S(2013)Multifocal hepatic cystic mass as first manifestation of metastatic spinal hemangiopericytoma Int J Surg Case Rep 1 15-18

[3] Turnani C(2010)Nasopharyngeal carcinoma with splenic and cystic liver metastases in a pediatric patient: 18F-FDG PET-CT findings Pediatr Radiol 40 S79-S82

[4] Djabri M(2008)One hundred years after “carcinoid”: epidemiology of and prognostic factors for neuroendocrine tumors in 35,825 cases in the United States J Clin Oncol 26 3063-3072

[5] Wiedemann R(2013)Clinical validation of the gastrointestinal NET grading system: Ki67 index criteria of the WHO 2010 classification is appropriate to predict metastasis or recurrence Diagn Pathol 8 65-959

[6] Sondag D(2007)Primary colorectal small cell carcinoma: a clinicopathological and immunohistochemical study of 10 cases Diagn Pathol 2 35-62

[7] Balibrea JM(2003)A 5-decade analysis of 13,715 carcinoid tumors Cancer 97 934-211

[8] Rovira-Argelagués M(2008)Consensus guidelines for the management of patients with liver metastases from digestive (neuro) endocrine tumors: foregut, midgut, hindgut, and unknown primary Neuroendocrinology 87 47-923

[9] Otero-Piñeiro AM(2006)Well-differentiated pancreatic non-functioning tumors/carcinoma Neuroendocrinology 84 196-143

[10] Julián JF(2012)Surgical strategy for liver metastases of neuroendocrine tumors Hepatogastroenterology 59 921-e259

[1] Estermann F(1996)Pseudocystic metastases of carcinoma of the uterine cervix mimicking polycystic liver disease Gastroenterol Clin Biol 12 1125-1128

[2] Thiebault S(2013)Multifocal hepatic cystic mass as first manifestation of metastatic spinal hemangiopericytoma Int J Surg Case Rep 1 15-18

[3] Turnani C(2010)Nasopharyngeal carcinoma with splenic and cystic liver metastases in a pediatric patient: 18F-FDG PET-CT findings Pediatr Radiol 40 S79-S82

[4] Djabri M(2008)One hundred years after “carcinoid”: epidemiology of and prognostic factors for neuroendocrine tumors in 35,825 cases in the United States J Clin Oncol 26 3063-3072

[5] Wiedemann R(2013)Clinical validation of the gastrointestinal NET grading system: Ki67 index criteria of the WHO 2010 classification is appropriate to predict metastasis or recurrence Diagn Pathol 8 65-959

[6] Sondag D(2007)Primary colorectal small cell carcinoma: a clinicopathological and immunohistochemical study of 10 cases Diagn Pathol 2 35-62

[7] Balibrea JM(2003)A 5-decade analysis of 13,715 carcinoid tumors Cancer 97 934-211

[8] Rovira-Argelagués M(2008)Consensus guidelines for the management of patients with liver metastases from digestive (neuro) endocrine tumors: foregut, midgut, hindgut, and unknown primary Neuroendocrinology 87 47-923

[9] Otero-Piñeiro AM(2006)Well-differentiated pancreatic non-functioning tumors/carcinoma Neuroendocrinology 84 196-143

[10] Julián JF(2012)Surgical strategy for liver metastases of neuroendocrine tumors Hepatogastroenterology 59 921-e259