Section: Hepatobiliary Sub-section: Liver Curriculum: Curriculum, page 85

Definition

  • Rare cystic tumour within liver parenchyma or bile ducts

Epidemiology

  • Mostly women
  • 4th decade

Risk factors

  • No association with OCP

Aetiology

  • Unclear

Pathology

  • Histologically
    • Lined by biliary-type mucus-secreting cuboidal or columnar epithelium, supported by fibrous stroma (representing ovarian tissue)
    • Some do not have ovarian-like stroma

Clinical

  • Cystadenomas are often found incidentally.
  • Larger cysts can be symptomatic and present with abdominal pain, abdominal fullness, early satiety and weight loss. Laboratory values are usually normal.

Investigations

  • USS
    • Hypoechoic with thickened, irregular wall, occasional internal echoes representing debris and wall nodularity – all features of complicated cyst.
  • CT and MRI can be organised to further diagnosis
  • Can be difficult to differentiate cystadenoma from cystadenocarcinoma
    • Presence of calcifications along with mixed solid and cystic components on imaging is associated with cystadenocarcinoma. 
    • Mural or septal nodule and a nodule diameter > 10 mm on conventional ultrasound are suggestive of cystadenocarcinoma.

Management

  • Thought to be precursor to Bilary cystadenocarcinoma
    • Cystadenocarcinoma are found to be more equally distributed in men and women
      • More aggressive in men
  • Aspiration or biopsy is not recommended as it has limited sensitivity and there is a risk of disseminating malignancy if there is an underlying cystadenocarcinoma. 
  • Treatment: Resection
    • Obtain histological diagnosis
    • Prevent malignant transformation