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By contrast, ing to the most recent figures reported by the FDA [20], BIA-ALCL carries a risk of mortality of about 5%.
Research has shown that 93% of people diagnosed with BIA-ALCL are still disease-free three years after treatment. Some people whove been treated for BIA-ALCL decide to have breast reconstruction surgery with smooth implants, flaps (autologous reconstruction), or fat grafting.
A kind of chemotherapy called CHOP is used for both ALK-positive and ALK-negative ALCL. The therapy gets its name for the first letters of the drugs it uses: Cytoxan, hydroxydaunorubicin, Oncovin, and prednisolone. If your cancer is ALK-negative, doctors may use CHOP at higher doses.
All patients diagnosed with BIA-ALCL requires implant removal and en bloc capsulectomy. In the presence of suspicious enlarged lymph nodes, surgical lymphadenectomy and bone marrow biopsy should be performed, with implant removal and en-bloc capsulectomy, to assess disease dissemination.
ALCL usually responds well to chemotherapy, and treatment may make it disappear. This is called remission. There is a risk that the lymphoma may come back in the future.
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Research has shown that 93% of people diagnosed with BIA-ALCL are still disease-free three years after treatment. Some people whove been treated for BIA-ALCL decide to have breast reconstruction surgery with smooth implants, flaps (autologous reconstruction), or fat grafting.
Common symptoms include breast enlargement, pain, asymmetry, lump in the breast or armpit, overlying skin rash, hardening of the breast, or a large fluid collection typically developing at least more than one year after receiving an implant, and on average after 8 to 10 years.
Common symptoms include breast enlargement, pain, asymmetry, lump in the breast or armpit, overlying skin rash, hardening of the breast, or a large fluid collection typically developing at least more than one year after receiving an implant, and on average after 8 to 10 years.

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