IJSR International Journal of Scientific Research 2277 - 8179 Indian Society for Health and Advanced Research ijsr-7-7-15843 Original Research Paper A CASE REPORT OF PRIMARY HEPATIC NEUROENDOCRINE TUMOUR Sharma Dr. July 2018 7 7 01 02 ABSTRACT

 INTRODUCTION: Primary hepatic neuroendocrine tumours are rare. Excluding extrahepatic origin of the tumour with liver metastasis is

important.
A 55year old male complaining of weight loss, intermittent fever, anorexia for 2 months .No abnormality detected CASE REPORT: in routine
investigations. On whole body CT–scan a rounded solitary space occupying hepatic lesion measuring 3.5x 3.4 was seen. USG–guided FNAC was
done. MGG stain smear shows small round cells with high N–C ratio, stippled chromatin and indistinct nucleoli. Further, IC staining shows
positivity with synaptophysin and chromogranin A which confirms the diagnosis of primary neuroendocrine tumour of liver.
CONCLUSION: PHNEC should be considered as a possible differential diagnosis in management of hepatic tumours. Surgical resection must be
considered for curative treatment.