“…The clinical hepatic neuroendocrine tumors mostly was induced by the transfer of intestines and pancreas and others (Pilichowska et al, 1999;Solcia et al, 2000;Modlin et al, 2008;Schwartz et al, 2008;Yao et al, 2008;Zeng et al, 2013) with the histopathologic performance of organ-like growth pattern, the tumor cells was argyrophilic, so they had specific positive performance in the detection of chromogranin A (CgA) and synaptophysin (Syn) of immunohistochemistry (Chang et al, 2007;Huang et al, 2010;Kim et al, 2011;Park et al, 2012). Primarily hepatic neuroendocrine carcinoma (PHNEC) was very rare, accounting for 1-5% of primary liver tumors, and 0.8%-4.0% of systemic neuroendocrine tumors (Pilichowska et al, 1999;Solcia et al, 2000;Yao et al, 2008;Huang et al, 2010).…”