Hepatic peliosis is a rare vascular condition characterized by the presence of blood-filled cystic spaces within the liver.
Unlike the typical vascular architecture of the liver, these spaces are not lined by endothelial cells, making them prone to rupture and bleeding.
This condition can be asymptomatic or present with non-specific symptoms such as abdominal pain, hepatomegaly (enlarged liver), or signs of liver dysfunction.
The etiology of hepatic peliosis is not fully understood, but it has been associated with a variety of factors, including chronic infections, malignancies, certain medications like anabolic steroids, and autoimmune diseases.
The condition is diagnosed using imaging studies such as ultrasound, computed tomography (CT), or magnetic resonance imaging (MRI), which can reveal the characteristic lesions.
In terms of management, treatment of hepatic peliosis depends on the underlying cause.
If associated with medication use, discontinuing the offending drug may result in resolution of the lesions.
In severe cases, or if complications such as hemorrhage occur, more invasive interventions may be required.
Monitoring and supportive care are essential components of managing individuals with this condition.