Can You Get Ovarian Cancer Without Fallopian Tubes?

Ovarian cancer begins when cells in or near the ovaries develop DNA changes. It is a serious gynecologic malignancy, often diagnosed at advanced stages because early symptoms are subtle and non-specific. This makes treatment more challenging, as approximately two-thirds of women are diagnosed when the disease has already spread.

The Emerging Link Between Fallopian Tubes and Ovarian Cancer

Recent scientific understanding has shifted the focus of high-grade serous ovarian cancer (HGSOC), the most common and aggressive type, from the ovary to the fallopian tubes. Research indicates that a significant proportion of these cancers, previously thought to originate in the ovaries, actually begin in the fimbriae. These delicate, finger-like projections are at the ends of the fallopian tubes, positioned close to the ovaries.

This discovery stems from detailed examinations of fallopian tubes, particularly in women with a high genetic risk for ovarian cancer. Pathologists identified early cancerous or pre-cancerous lesions, termed serous tubal intraepithelial carcinoma (STIC lesions), predominantly within the fimbrial ends of the fallopian tubes. STIC lesions are considered potential precursors to HGSOC.

STIC lesions imply cancer cells can originate in the fallopian tube, then shed onto the ovary or into the abdominal cavity to grow. This understanding highlights the fallopian tubes, specifically their fimbrial ends, as a primary site of origin for many HGSOC cases, rather than the ovaries. This emphasizes the fallopian tubes’ importance in ovarian cancer prevention strategies.

Ovarian Cancer Risk After Fallopian Tube Removal

The surgical removal of fallopian tubes, known as a salpingectomy, significantly reduces ovarian cancer risk, though it does not eliminate it entirely. A bilateral salpingectomy, removing both fallopian tubes while leaving ovaries intact, can reduce risk by approximately 80%. For higher-risk individuals, such as those with BRCA gene mutations, a bilateral salpingo-oophorectomy (removing both fallopian tubes and ovaries) offers greater risk reduction.

Even after removing ovaries and fallopian tubes, primary peritoneal cancer (PPC) can develop. PPC arises from the peritoneum, the abdominal cavity’s thin lining. Peritoneal cells are embryologically similar to ovarian and fallopian tube cells, explaining why PPC behaves and is treated like epithelial ovarian cancer. PPC can occur years after a bilateral salpingo-oophorectomy, showing that complete risk elimination is not possible through surgery alone.

Other rarer ovarian cancer types do not primarily originate in the fallopian tubes. These include germ cell tumors, which arise from egg-producing cells and typically affect younger individuals, and stromal cell tumors, which develop from hormone-producing connective tissue cells. These less common types account for 10-15% of cases. While fallopian tube removal is a powerful preventive measure for the most common ovarian cancer type, it does not protect against all forms of the disease.

Understanding Other Ovarian Cancer Risk Factors and Symptoms

Several factors contribute to ovarian cancer risk. Age is a primary factor, with most cancers developing after menopause, typically in women aged 63 or older. A family history of ovarian or breast cancer also increases risk, especially if close relatives have been affected. Inherited gene mutations, such as BRCA1 and BRCA2, significantly elevate lifetime risk (35-70% for BRCA1, 10-30% for BRCA2 carriers). Other genetic changes, including those linked to Lynch syndrome and mutations in BRIP1, RAD51C, and RAD51D, also increase susceptibility.

Reproductive factors can influence risk. These include never having been pregnant, starting menstruation early, or experiencing menopause late. Endometriosis, where tissue similar to the uterine lining grows outside the uterus, is another risk factor. Hormone replacement therapy after menopause may also slightly increase risk.

Ovarian cancer symptoms are often subtle and non-specific, making early detection challenging. Common symptoms include persistent abdominal bloating or swelling, pelvic or abdominal pain, and feeling full quickly. Changes in bowel habits (constipation or diarrhea) and urinary symptoms (frequent or urgent urination) can also occur. Other symptoms may include fatigue, back pain, and unexplained weight changes. While these symptoms are common and often caused by less serious conditions, seek medical attention if they are new, persistent, and occur frequently (12 or more times a month).