Borderline ovarian tumours represent a distinct group of ovarian neoplasms with low malignant potential. They are not benign lesions, but they are also not invasive ovarian cancer.
They are characterised by cellular atypia without stromal invasion, which distinguishes them from invasive ovarian malignancies.
Key characteristics
Borderline ovarian tumours:
- occur more frequently in younger women
- are associated with an excellent prognosis
- tend to grow more slowly than invasive ovarian cancer
- are often diagnosed at an early stage
The most common histological subtypes include:
Symptoms
Symptoms are often non-specific and may include:
- abdominal bloating or distension
- mild abdominal or pelvic discomfort
- a sensation of pelvic pressure
In many cases, these tumours are detected incidentally during imaging or surgery for other indications.
How are borderline ovarian tumours diagnosed
Diagnosis is based on:
- pelvic ultrasound
- imaging investigations (MRI or CT), where appropriate
- surgical removal of the lesion followed by histological examination
A definitive diagnosis can only be made after histopathological assessment.
How are borderline ovarian tumours treated
The mainstay of treatment is surgical management.
The extent of surgery depends on:
- the patient’s age
- disease stage
- fertility preservation considerations
In selected cases, fertility-sparing surgery may be performed, preserving the uterus and/or one ovary.
Prognosis and follow-up
The prognosis of borderline ovarian tumours is excellent in the vast majority of cases.
Nevertheless, regular follow-up with clinical and imaging assessment is recommended, particularly after fertility-sparing treatment.