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What is Uterine Carcinosarcoma (MMMT)

Uterine Carcinosarcoma (MMMT) description. Find out what Uterine Carcinosarcoma (MMMT) is and know more about it.

What is Uterine Carcinosarcoma (MMMT)

Uterine Carcinosarcoma (MMMT) is a rare and aggressive type of cancer that affects the uterus. It is also known as malignant mixed Müllerian tumor (MMMT). This cancer is characterized by the presence of both carcinomatous (epithelial) and sarcomatous (mesenchymal) components.


Uterine carcinosarcoma typically arises in postmenopausal women, although it can occur in younger women as well. The exact cause of this cancer is unknown, but certain risk factors such as older age, prior radiation therapy, and a history of certain benign uterine conditions may increase the likelihood of developing it.


The symptoms of uterine carcinosarcoma may include abnormal vaginal bleeding, pelvic pain, and a mass or lump in the pelvic area. Diagnosis is usually made through a combination of imaging tests, biopsies, and histological examination.


Treatment for uterine carcinosarcoma often involves a combination of surgery, chemotherapy, and radiation therapy. The prognosis for this cancer is generally poor, as it tends to be aggressive and can spread to other parts of the body.


Regular check-ups and early detection are crucial in managing uterine carcinosarcoma. It is important to consult with a healthcare professional for personalized advice and treatment options.


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What is Uterine Carcinosarcoma (MMMT)

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World map of Uterine Carcinosarcoma (MMMT)

Find people with Uterine Carcinosarcoma (MMMT) through the map. Connect with them and share experiences. Join the Uterine Carcinosarcoma (MMMT) community.

Stories of Uterine Carcinosarcoma (MMMT)

UTERINE CARCINOSARCOMA (MMMT) STORIES
Uterine Carcinosarcoma (MMMT) stories
There are more details of my experience on www.thepencilledactress.com. my mum has this cancer and is deemed incurable. please feel free to contact me at any time x 
Uterine Carcinosarcoma (MMMT) stories
My mother was diagnosed with this about 10 yrs ago. I did a lot of Google research which was insanely scary. I made a group on FB and have now over 500 members. When you have actual people telling their personal stories, it's not so scary.

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Uterine Carcinosarcoma (MMMT) forum

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