Uterine adenosarcoma

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Uterine Adenosarcoma

Uterine adenosarcoma is a rare type of cancer that affects the uterus. It is characterized by the presence of both malignant and benign components within the tumor. The malignant component consists of stromal cells that have the potential to spread to other parts of the body, while the benign component consists of glandular cells that do not have the ability to metastasize.

Symptoms[edit | edit source]

Symptoms of uterine adenosarcoma may include abnormal vaginal bleeding, pelvic pain, and a feeling of fullness in the lower abdomen. Some women may also experience pain during intercourse or have a mass or lump in the pelvic area.

Diagnosis[edit | edit source]

Diagnosis of uterine adenosarcoma typically involves a combination of imaging tests, such as ultrasound and MRI, as well as a biopsy of the tumor to confirm the presence of both malignant and benign components.

Treatment[edit | edit source]

Treatment for uterine adenosarcoma usually involves surgery to remove the tumor and surrounding tissue. In some cases, radiation therapy or chemotherapy may be recommended to help prevent the cancer from recurring.

Prognosis[edit | edit source]

The prognosis for uterine adenosarcoma depends on various factors, including the stage of the cancer at the time of diagnosis and the presence of any underlying health conditions. Early detection and treatment can improve the chances of successful outcomes.

Epidemiology[edit | edit source]

Uterine adenosarcoma is a rare type of cancer, accounting for less than 5% of all uterine malignancies. It most commonly affects women in their 40s and 50s, although it can occur at any age.

References[edit | edit source]


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Contributors: Prab R. Tumpati, MD