Fluid around capsule of breast implant

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But in recent years, some people have suspected that their breast implants have made them very ill with diseases such as:. Older studies showed no clear scientific evidence connecting these conditions to breast implants — silicone or saline-filled. However, newer studies from different sources have found an association between silicone breast implants and certain autoimmune diseases. The World Health Organization and the U. Food and Drug Administration have identified another possible cause for concern. Scientists say this could be due to the fact that textured implants have a greater surface area on which a bacterial infection can form.
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U.S. Food and Drug Administration

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What is capsular contracture and how can it be treated? | ASPS

As a result, the breast may feel painful and stiff, and the capsule may affect the appearance or shape of the breast. Capsules actually form around every breast implant, silicone or saline. It is only when that scar tissue tightens or contracts and restricts the movement of the implant that the breast may develop capsular contracture. Symptoms of capsular contracture often begin within months of the original breast augmentation surgery, but capsular contracture can occur at any time. About 75 percent of capsules occur within the first two years following surgery.
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Formal Treatment Guidelines Developed for Rare Cancer Linked to Breast Implants

Sometimes, no matter how skilled a patient's plastic surgeon is, complications arise during or after surgery. This is the case because everyone's body is different. The composition of connective tissue varies widely from one patient to another, for instance, and this means that each patient's healing process is entirely unique. This is why some people tend to develop thick scar tissue after any kind of penetrating skin injury, while others can sustain deep cuts and develop only subtle scarring that fades over time. Another good example of this difference is the way some women will develop severe stretch marks during pregnancy no matter what they do to prevent them, whereas other women emerge from pregnancy nearly stretch mark-free.
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At that time, the FDA knew of so few cases of this disease that it was not possible to determine what factors increased the risk. In a report summarizing the Agency's findings, we emphasized the need to gather additional information to better characterize ALCL in individuals with breast implants. In , the World Health Organization designated breast implant-associated anaplastic large cell lymphoma BIA-ALCL as a T-cell lymphoma that can develop following breast implants and noted that the exact number of cases remained difficult to determine due to significant limitations in world-wide reporting and lack of global breast implant sales data. Since that time, the FDA has undertaken several steps to better understand this issue, including an in-depth review of post-approval study data, medical device reports, scientific literature and breast implant-specific registries, and public discussions.
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