Attorney Jessie Paluch, founder of TruLaw, has over 25 years of experience as a personal injury and mass tort attorney, and previously worked as an international tax attorney at Deloitte. Jessie collaborates with attorneys nationwide — enabling her to share reliable, up-to-date legal information with our readers.
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On March 21, the U.S. Food and Drug Administration (FDA) released a statement that a rare type of non-Hodgkin’s lymphoma can develop after a person receives breast implants, based on more than 350 reports of this type of cancer and its connection to breast implants.
But how do breast implants increase cancer risk?
Exactly how breast implants may cause anaplastic large cell lymphoma (ALCL) remains largely unknown, but a 2016 paper published in the Aesthetic Surgery Journal suggests that chronic inflammation could play a role.
Some studies have found markers of chronic inflammation contained in the scar tissue around breast implants, which may suggest that an immune response to the implants could trigger cancer.
According to the FDA, women with breast implants have a very low but increased risk of developing ALCL compared to those who do not have breast implants.
Research has also shown that ALCL occurs more commonly in women who receive breast implants that feature a textured surface, as compared to those whose implants have a smooth surface.
Of the 231 reports of ALCL received by the FDA, 203 related to textured implants, while only 28 involved smooth implants.
Although it is not clear why the risk of cancer is higher among those with textured breast implants, the body appears to react differently to the textured ones.
According to the FDA, those who developed ALCL ranged in age from 25 to 91, and the average time between the implant surgery and the cancer diagnosis was seven years, although, in at least one case, the time period was 40 years.
The agency advised that those who are considering breast implants should speak with their physicians concerning the risks and benefits of textured implants versus smooth implants, and comply with all recommended follow-up care if they already have implants.
Experienced Attorney & Legal SaaS CEO
With over 25 years of legal experience, Jessie is an Illinois lawyer, a CPA, and a mother of three. She spent the first decade of her career working as an international tax attorney at Deloitte.
In 2009, Jessie co-founded her own law firm with her husband – which has scaled to over 30 employees since its conception.
In 2016, Jessie founded TruLaw, which allows her to collaborate with attorneys and legal experts across the United States on a daily basis. This hypervaluable network of experts is what enables her to share reliable legal information with her readers!
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Camp Lejeune’s water contamination issue spanned several decades starting in the 1950s. Exposure to these chemicals has been linked to various serious health issues, including cancer, organ diseases, and death.
Research is increasingly suggesting a link between the use of Tylenol during pregnancy and the development of neurodevelopmental disorders, such as autism and ADHD, in infants.
Legal action is being taken against manufacturers of Aqueous Film-Forming Foam (AFFF), a chemical used in fighting fires. The plaintiffs allege that exposure to the foam caused health issues such as cancer, organ damage, and birth and fertility issues.
Here, at TruLaw, we’re committed to helping victims get the justice they deserve.
Alongside our partner law firms, we have successfully collected over $3 Billion in verdicts and settlements on behalf of injured individuals.
Would you like our help?
Fresenius Kabi USA, LLC has announced a corrective Class I recall of an infusion pump software, LVP Software, that runs on the Ivenix Infusion System (IIS). Initiated by the firm on March 7, 2024, the action comes after multiple software anomalies were identified and found
According to the FDA, 20-ounce packages of “King Kullen Broccoli Cutlets with Bread Crumbs and Parmesan” have been recalled by New Haven, Connecticut-based Gracie’s Kitchen due to the potential presence of undeclared sesame and wheat. Individuals who live with allergies to either allergen are advised
The FDA is warning consumers of a Class I recall of Boston Scientific’s Obsidio Comformable Embolic because the device has been shown to present a risk for increased bowel ischemia when used for lower GI (gastrointestinal) bleeding, or acute colonic bleeding. As a pre-mixed embolic