Description
Neuroendocrine prostate cancer (NEPC) is rare historically but may  be  increasingin  prevalence  as  patients  potentially  develop  resistance  to contemporary  anti-androgen  treatment  through  a  neuroendocrine  phenotype.  Diagnosis  can   be   straightforward   when  classic  morphological   features  are accompanied  by  a  prototypical  immunohistochemistry  profile,  however  there  is increasing  recognition  of  disease  heterogeneity  and  hybrid  phenotypes.    In  the primary setting, small cell prostatic carcinoma (SCPC) is frequently admixed with adenocarcinomas that may be clonally related, while a small fraction of SCPCs express markers typical of prostatic adenocarcinoma.  Gene expression patterns may  eventually  help  elucidate  the  biology  underlying  equivocal  cases  with discordant IHC, however studies to date have focused on prototypical cases and been based on few patients due to disease rarity.