Brenner tumour

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Brenner tumour
File:Brenner Tumor of Ovary.jpg
Synonyms Brenner tumor
Pronounce N/A
Specialty N/A
Symptoms Often asymptomatic, may present with abdominal pain or pelvic mass
Complications Rarely malignant transformation
Onset Typically in postmenopausal women
Duration Variable
Types Benign, Borderline, Malignant
Causes Unknown
Risks Age, hormonal factors
Diagnosis Histopathology, imaging studies
Differential diagnosis Ovarian cyst, fibroma, thecoma
Prevention None known
Treatment Surgical excision
Medication Not typically used
Prognosis Excellent for benign tumors
Frequency Rare
Deaths Rare, associated with malignant cases


Brenner tumour is a rare type of ovarian tumor that is part of the surface epithelial-stromal tumor group. These tumors are typically benign, but can occasionally be malignant. They are named after the German pathologist Fritz Brenner, who first described them in 1907.

Histology[edit]

File:Brenner tumour intermed mag.jpg
Brenner tumour at intermediate magnification

Brenner tumours are characterized histologically by the presence of transitional epithelium, similar to that found in the urinary bladder. The stroma of the tumor is typically fibrous and may contain Walthard cell rests, which are nests of transitional epithelial cells.

File:Walthard cell rest - very high mag.jpg
Walthard cell rest at very high magnification

The epithelial component of Brenner tumours often forms nests or islands within the fibrous stroma. These nests are composed of cells with abundant cytoplasm and oval nuclei, which may exhibit the characteristic "coffee bean" appearance due to longitudinal nuclear grooves.

Clinical Presentation[edit]

Brenner tumours are most commonly found in postmenopausal women, typically between the ages of 50 and 70. They are often asymptomatic and are usually discovered incidentally during pelvic examinations or imaging studies for other conditions. When symptoms do occur, they may include abdominal pain or a palpable mass.

Diagnosis[edit]

The diagnosis of a Brenner tumour is primarily made through histological examination of the tumor tissue. Imaging studies such as ultrasound or CT scan may suggest the presence of an ovarian mass, but definitive diagnosis requires microscopic evaluation.

File:Brenner tumor with annotated coffee bean nuclei.jpg
Brenner tumor with annotated coffee bean nuclei

On microscopic examination, the presence of transitional epithelial cells with "coffee bean" nuclei within a fibrous stroma is diagnostic of a Brenner tumour.

Treatment[edit]

The treatment of Brenner tumours depends on their nature. Benign Brenner tumours are typically treated with surgical removal, which is often curative. Malignant Brenner tumours require more extensive surgical intervention and may be treated with additional therapies such as chemotherapy or radiation, depending on the stage and spread of the disease.

Prognosis[edit]

The prognosis for patients with benign Brenner tumours is excellent, as these tumors do not metastasize and are cured by surgical removal. Malignant Brenner tumours have a more guarded prognosis, depending on the extent of the disease and response to treatment.

See also[edit]