DOI: 10.36347/sjmcr.2022.v10i07.005

Pages: 622-624

Hepar lobatum carcinomatosum is a rare liver disease acquired during the evolution of a carcinoma metastatic to the liver, corresponds to a hepatic dysmorphia of non-cirrhotic origin associating signs of portal hypertension. We report the case of a patient who presented signs of portal hypertension without a context of chronic hepatitis, an aspect of dysmorphic liver without hepatocellular carcinoma is documented by CT imaging, suspecting a hepar lobatum carcinomatosum, from which a clinical, biological, radiological and histological diagnostic approach was instituted concluding to a breast ductal carcinoma.