Primary Peritoneal Hepatoid Adenocarcinoma: A Multidisciplinary Approach for a Rare Case Scenario
摘要
Primary hepatoid adenocarcinoma of the peritoneum (PHAP) is a rare but important subtype of extrahepatic adenocarcinoma, often mistaken for hepatocellular carcinoma (HCC), which makes diagnosis and treatment optimization challenging. To date, hepatoid adenocarcinoma of primary peritoneal origin has been reported only in case studies, limiting the data on managing its distinct behavior.
DiscussionAccurate diagnosis of PHAP is critical for prognosis. PHAP should be considered in middle-aged or elderly patients presenting with elevated serum alpha-fetoprotein (AFP) levels and atypical hepatic imaging findings. Immunohistochemical staining is key to differentiating PHAP from HCC.
ConclusionPHAP is a rare and aggressive disease with significant diagnostic and therapeutic challenges. A multidisciplinary approach is essential for accurate diagnosis and management. More data are needed to establish standardized treatment protocols.