Section Editor: Kianoosh Keyhanian MD FRCPC
May 25, 2026
A borderline Brenner tumor of the ovary is an uncommon type of ovarian tumor that is not cancer, but is also not a completely benign growth. It belongs to a group of tumors called borderline tumors, which sit between clearly benign tumors and cancer. A borderline Brenner tumor is more complex than a benign Brenner tumor, but it does not grow into the surrounding tissue the way a cancer does. It is made up of cells that look more crowded and more abnormal than those of a benign Brenner tumor, while still remaining within the surface layer of the tumor.
Borderline Brenner tumor is also called atypical proliferative Brenner tumor, and you may see that term on your pathology report. It is the least common of the borderline ovarian tumors, and only a small number of cases have been described. It is almost always found in one ovary, and it most often occurs in women after menopause. The outlook is very good, and most patients are cured by surgery alone.
This article will help you understand what this diagnosis means on your pathology report, what each term means, and why it matters for your care.
The exact cause of a borderline Brenner tumor is not well understood. Brenner tumors are made up of a type of cell that resembles the cells lining the bladder and urinary tract, and they are thought to develop from small groups of these cells found near the ovary and fallopian tube. The process that leads a Brenner tumor to develop the more crowded, more abnormal features of a borderline tumor is not known. Unlike some ovarian cancers, borderline Brenner tumors do not have a well-defined set of risk factors, such as specific inherited gene changes or a family history. It is not caused by an infection and is not contagious.
Many borderline Brenner tumors cause no symptoms, particularly when they are small, and are discovered during an imaging test or surgery performed for another reason. When symptoms do occur, they are usually related to the presence of a mass in the ovary and may include:
Because these symptoms are common and can have many causes, they are not specific to a borderline Brenner tumor. Any persistent abdominal or pelvic symptom should be evaluated by a doctor.
The diagnosis of a borderline Brenner tumor is made after the tumor is surgically removed and examined under the microscope by a pathologist. Imaging studies such as ultrasound, CT, or MRI may show an ovarian mass, but they cannot reliably tell a borderline tumor apart from a benign or a cancerous tumor. The diagnosis can only be confirmed by examining the tissue.
Under the microscope, the pathologist looks for the crowded, more abnormal-looking cells of a borderline Brenner tumor and, importantly, confirms that these cells do not grow into the surrounding tissue. To support the diagnosis and tell this tumor apart from other types of ovarian tumors, the pathologist may perform a test called immunohistochemistry, which detects specific proteins inside the tumor cells.
When examined under the microscope, a borderline Brenner tumor shows several characteristic features:
A borderline Brenner tumor is often found alongside an area of benign Brenner tumor, and in some cases a mucinous tumor is present in the same ovary.
All ovarian tumors are examined to see whether there are any holes or tears in the outer surface of the tumor or ovary. This outer surface is called the capsule.
The pathologist also examines the surface of the ovary under the microscope to determine whether any tumor cells are present. A ruptured capsule, or tumor cells found on the surface of the ovary, raises the pathologic stage. For a borderline Brenner tumor, however, the capsule is usually intact and the tumor is confined to the ovary.
Even though a borderline Brenner tumor is not cancer, it is given a pathologic stage using the same system used for ovarian cancers, the FIGO staging system. The stage describes how much of the tumor was found beyond the ovary itself. Almost all borderline Brenner tumors are stage I, meaning the tumor is confined to the ovary.
Stages II, III, and IV are very rare for a borderline Brenner tumor. When a Brenner tumor appears to involve tissue beyond the ovary, the pathologist carefully reconsiders whether the tumor may instead be a malignant Brenner tumor.
The prognosis for a borderline Brenner tumor is very good. Almost all of these tumors are confined to one ovary at the time of diagnosis, and surgical removal alone is curative for the great majority of patients. Because the tumor does not invade the surrounding tissue, it does not behave like cancer. Recurrence after complete removal is very rare; only isolated cases have been reported in the medical literature. The most important factor for a good outcome is complete surgical removal of the tumor.
Surgery is the main treatment for a borderline Brenner tumor, and for most patients it is the only treatment needed. The discussion between you and your gynecologic team about the type of surgery depends on your age, whether you wish to preserve the ability to become pregnant, and the findings on your pathology report.
Options that the team may discuss include:
After treatment, follow-up with a gynecologist or gynecologic oncologist is recommended.