Systemic inflammatory disease resolution following cosmetic silicone breast implant removal.
Journal: 2015/October - BMJ Case Reports
ISSN: 1757-790X
Abstract:
A 37-year-old Caucasian woman presented with subacute, symmetrical inflammatory arthralgia, which was affecting her work. Apart from fatigue, she had no other constitutional symptoms. She had undergone cosmetic bilateral silicone breast implant surgery in 2008. Blood tests revealed erythrocyte sedimentation rate 53 mm/h, weakly positive antinuclear antibodies and IgG cardiolipin antibody, while breast ultrasound revealed a ruptured left silicone implant. The working diagnosis was systemic inflammatory disease of uncertain origin. She decided to have replacement, rather than removal, of her silicone breast implants privately, but her symptoms persisted postoperatively with a new erythema multiforme-like rash despite treatment with methotrexate and moderate dose prednisolone. Following further consultation with a National Health Service breast surgeon, her silicone implants were removed. Within 10 weeks of surgery, all immunomodulatory treatment was discontinued with complete symptom and inflammatory response resolution. This case illustrates that implant silicone can induce clinically significant systemic inflammatory disease and implant removal is essential for disease resolution.
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BMJ Case Rep 2015: bcr2014207418

Systemic inflammatory disease resolution following cosmetic silicone breast implant removal

Department of Dermatology, Sandwell and West Birmingham Hospitals NHS Trust, Birmingham, West Midlands, UK
Department of Rheumatology, Dudley Group NHS Foundation Trust, Dudley, West Midlands, UK
Department of Plastic Surgery, Dudley Group NHS Foundation Trust, Dudley, West Midlands, UK
Dr Rainer Klocke, ku.shn.hgd@ekcolK.reniaR
Dr Rainer Klocke, ku.shn.hgd@ekcolK.reniaR
Accepted 2015 Jan 9.

Abstract

A 37-year-old Caucasian woman presented with subacute, symmetrical inflammatory arthralgia, which was affecting her work. Apart from fatigue, she had no other constitutional symptoms. She had undergone cosmetic bilateral silicone breast implant surgery in 2008. Blood tests revealed erythrocyte sedimentation rate 53 mm/h, weakly positive antinuclear antibodies and IgG cardiolipin antibody, while breast ultrasound revealed a ruptured left silicone implant. The working diagnosis was systemic inflammatory disease of uncertain origin. She decided to have replacement, rather than removal, of her silicone breast implants privately, but her symptoms persisted postoperatively with a new erythema multiforme-like rash despite treatment with methotrexate and moderate dose prednisolone. Following further consultation with a National Health Service breast surgeon, her silicone implants were removed. Within 10 weeks of surgery, all immunomodulatory treatment was discontinued with complete symptom and inflammatory response resolution. This case illustrates that implant silicone can induce clinically significant systemic inflammatory disease and implant removal is essential for disease resolution.

Abstract
Learning points

Footnotes

Contributors: FM and SAC were involved in reviewing the case and drafting the manuscript. SW had essential involvement in the management and discussion of case. RK had clinical responsibility for the case, reviewed the literature and had final input in the submitted version of the manuscript.

Competing interests: None.

Patient consent: Obtained.

Provenance and peer review: Not commissioned; externally peer reviewed.

Footnotes

References

  • 1. Janowsky EC, Kupper LL, Hulka BS. Meta-analyses of the relation between silicone breast implants and the risk of connective-tissue diseases. N Engl J Med 2000;342:781–90. 10.1056/NEJM200003163421105 [] [[PubMed]
  • 2. Lipworth L, Holmich LR, McLaughlin JK. Silicone breast implants and connective tissue disease: no association. Semin Immunopathol 2011;33:287–94. 10.1007/s00281-010-0238-4 [] [[PubMed]
  • 3. Keogh B. Poly implant prosthese (PIP) breast implants: final report of the expert group. June 2012. [PubMed]
  • 4. Cohen Tervaert JW, Kappel RM. Silicone implant incompatibility syndrome (SIIS): a frequent cause of ASIA (Shoenfeld's syndrome). Immunol Res 2013;56:293–8. 10.1007/s12026-013-8401-3 [] [[PubMed]
  • 5. Shoenfeld Y, Agmon-Levin N. ‘ASIA’ Autoimmune/inflammatory syndrome induced by adjuvants. J Autoimmunity 2006;36:4–8. 10.1016/j.jaut.2010.07.003 [] [[PubMed]
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