Brenner tumour

Brenner tumour is a rare type of ovarian neoplasm that is part of the surface epithelial-stromal tumour group of ovarian cancers. It was first described by Robert Brenner in 1907.

Overview[edit | edit source]

Brenner tumours are typically benign, but can sometimes be malignant or borderline. They are usually asymptomatic and are often discovered incidentally during routine gynaecological examinations.

Brenner tumours are composed of small, round, uniform cells that resemble transitional epithelium (the type of tissue that lines the urinary tract). These cells are typically arranged in nests surrounded by dense fibrous tissue.

Clinical Features[edit | edit source]

Most Brenner tumours are asymptomatic, but some women may experience pelvic pain or pressure. On physical examination, a pelvic mass may be palpable.

Diagnosis[edit | edit source]

The diagnosis of Brenner tumour is usually made based on the histological appearance of the tumour. Imaging studies such as ultrasound, CT scan, or MRI may also be used to identify the tumour.

Treatment[edit | edit source]

The treatment for Brenner tumour is usually surgical removal of the tumour. In some cases, chemotherapy or radiation therapy may be used if the tumour is malignant.

Prognosis[edit | edit source]

The prognosis for women with Brenner tumour is generally good, especially if the tumour is benign. However, malignant Brenner tumours can be more aggressive and have a poorer prognosis.

References[edit | edit source]

Brenner tumour Resources
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