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Vulvar cancer is a rare form of cancer affecting the vulva and the external genital organs in women. It accounts for less than 1% of all cancer cases in the UK.
The cancer rarely affects the young and most commonly affects women over 65.
The lifetime risk in the UK is 1 in 316 women.
In the United States, vulvar cancer accounts for about 4% of cancers of the female reproductive organs and 0.6% of all cancers in women. In the US, women have a 1 in 406 chance of developing vulvar cancer during their lifetime. (1-5)
Most vulvar cancers are of squamous cell carcinoma type – around 75 to 85%. The rest are of various other types like melanoma, adenocarcinoma etc.
In half of the cases the labia majora – the external lips of the vulva is affected. The inner lips or labia minora is affected in nearly 205 cases. In small number of cases the glands and the clitoris is affected.
Cancer starts when the blue print within the cells called the DNA and genes are altered. This leads to uncontrolled multiplication of the affected cells till they invade surrounding cells.
Vulvar cancer spreads in three major ways. It spreads out of the vulvar tissue into surrounding parts of the body like the urethral opening and the vagina.
It may also spread via the lymphatic channels and lymph nodes to affect the whole body. The first lymph nodes that are invaded are the nearest ones in the groin.
The cancer may also spread via blood vessels to large organs like liver, lungs and brain. Cancer that has spread to other parts of the body is known as metastatic cancer.
Exact cause of vulvar cancer is unknown. However some risk factors may play a role in this cancer. Risk factors of vulvar cancer include:
Other risk factors associated with vulvar cancer include: