Hepatoid
adenocarcinoma (HAC) is a
tumor with aberrant hepatocellular differentiation that occurs in extrahepatic organs. HAC of the gallbladder is rare, and cases of
alpha-fetoprotein production are extremely rare. A 61-year-old man was diagnosed with gallbladder
adenocarcinoma after
laparoscopic cholecystectomy. A radical operation including resection of liver bed and
lymph node dissection was performed, and no
tumor cell was found. However, at postoperative 19 months, he showed
lymphadenopathy of the portocaval area and
tumor thrombi in the right portal vein with high levels of serum
alpha-fetoprotein. After right hemihepatectomy and portahepatis
lymph node dissection was performed, he was diagnosed with metastatic HAC. On reviewing the gallbladder specimen, the
tumor finally demonstrated HAC as the primary origin. Despite adjuvant
therapy, the patient died from multiple liver
metastasis 26 months after
cholecystectomy. Although HAC of the gallbladder is a very rare
malignancy, awareness of its existence is critical to avoid misdiagnosis.