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Cystic Primary Hepatic Neuroendocrine Tumor.

Jin Mo KimWon Ae LeeHyun Deok ShinIl Han SongSuk Bae Kim
Published in: The Korean journal of gastroenterology = Taehan Sohwagi Hakhoe chi (2021)
Neuroendocrine tumors (NETs) can arise throughout the body. Most NETs in the liver are metastatic tumors; primary hepatic NET (PHNET) is extremely rare. A diagnosis of PHNET is very difficult. No single modality can diagnose PHNET by itself, and it often resembles other hypervascular masses of the liver. This paper reports the case of a 51-year old female with a large hepatic mass. Unlike most of PHNETs reported previously, it was composed of a solid mass with mainly multiple cystic lesions, which led to an erroneous diagnosis of hepatic mucinous cystadenoma or cystadenocarcinoma. PHNET with cystic lesions is extremely rare, and the features are not well studied. This case may help physicians suspect PHNET in a differential diagnosis of an atypical hepatic mass.
Keyphrases
  • neuroendocrine tumors
  • squamous cell carcinoma
  • small cell lung cancer
  • primary care
  • magnetic resonance imaging
  • emergency department
  • computed tomography
  • magnetic resonance