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
- Cystadenocarcinoma are found to be more equally distributed in men and women
- 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