<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" article-type="Case Report" dtd-version="1.0"><front><journal-meta><journal-id journal-id-type="pmc">iajabms</journal-id><journal-id journal-id-type="pubmed">IAJABMS</journal-id><journal-id journal-id-type="publisher">IAJABMS</journal-id><issn>2709-3298</issn></journal-meta><article-meta><article-id pub-id-type="doi">https://doi.org/10.47310/iajabms.2022.v03i01.003</article-id><title-group><article-title>Hepatoid Adenocarcinoma of Gall Bladder: Case Report and Literature Review</article-title></title-group><contrib-group><contrib contrib-type="author"><name><given-names>Ritu</given-names><surname>Sharma</surname></name></contrib></contrib-group><contrib-group><contrib contrib-type="author"><name><given-names>Kaalindi</given-names><surname>Singh</surname></name></contrib></contrib-group><contrib-group><contrib contrib-type="author"><name><given-names>RR</given-names><surname>Negi</surname></name></contrib></contrib-group><aff-id id="aff-a" /><abstract>Hepatoid adenocarcinoma (HAC) is a rare tumor with hepatocellular differentiation arising from extrahepatic tissue. Morphologically this tumor exhibits both adenocarcinomatous and hepatocellular differentiation and most of the tumors shows immunohistochemical staining for alpha-fetoprotein or elevated AFP levels. HAC of gall bladder is very rarely reported in literature. Tumor is most commonly found in stomach as a specific subtype of primary gastric carcinoma with occasional reports describing location in other organs like lung, kidney, female reproductive tract, pancreas and gall bladder. Here we present a case of 61 year old female patient with HAC gall bladder.&amp;nbsp;</abstract></article-meta></front><body /><back /></article>