Thoracic Outlet Syndrome Following Breast Implant Rupture
Summary: We present a patient with bilateral breast implant rupture who developed severe locoregional silicone granulomatous lymphadenopathy. Poly Implant Prothese silicone implants had been used for bilateral breast augmentation 5 years prior. Extracapsular implant rupture and bilateral axillary ly...
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Wolters Kluwer
2015-03-01
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doaj-cd5fcb9cb51341dcb1e3c833c7bc5dbd2020-11-24T22:31:46ZengWolters KluwerPlastic and Reconstructive Surgery, Global Open2169-75742015-03-0133e33110.1097/GOX.000000000000029501720096-201503000-00017Thoracic Outlet Syndrome Following Breast Implant RuptureRaakhi Mistry, MBChB0Yugesh Caplash, MBBS, FRACS1Pratyush Giri, MBBS, FRACP, FRCPA2Daniel Kearney, MBBS, FRCPA3Marcus Wagstaff, MBBS, PhD, FRACS4From the Department of Plastic and Reconstructive Surgery, Royal Adelaide Hospital, North Terrace, Adelaide, South AustraliaFrom the Department of Plastic and Reconstructive Surgery, Royal Adelaide Hospital, North Terrace, Adelaide, South AustraliaDepartment of Haematology, Royal Adelaide Hospital, North Terrace, Adelaide, South Australia;Anatomical Pathology, SA Pathology, Royal Adelaide Hospital, North Terrace, Adelaide, South Australia.From the Department of Plastic and Reconstructive Surgery, Royal Adelaide Hospital, North Terrace, Adelaide, South AustraliaSummary: We present a patient with bilateral breast implant rupture who developed severe locoregional silicone granulomatous lymphadenopathy. Poly Implant Prothese silicone implants had been used for bilateral breast augmentation 5 years prior. Extracapsular implant rupture and bilateral axillary lymphadenopathy indicated explantation, capsulectomy, and selective lymph node excision. Histology demonstrated silicone lymphadenopathy with no evidence of malignancy. Over the subsequent 12 months, she developed progressive locoregional lymphadenopathy involving bilateral cervical, axillary, and internal mammary groups, resulting in bilateral thoracic outlet syndrome. We report the unusual presentation, progression, and the ultimate surgical management of this patient.http://journals.lww.com/prsgo/Fulltext/2015/03000/Article.17.aspx |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Raakhi Mistry, MBChB Yugesh Caplash, MBBS, FRACS Pratyush Giri, MBBS, FRACP, FRCPA Daniel Kearney, MBBS, FRCPA Marcus Wagstaff, MBBS, PhD, FRACS |
spellingShingle |
Raakhi Mistry, MBChB Yugesh Caplash, MBBS, FRACS Pratyush Giri, MBBS, FRACP, FRCPA Daniel Kearney, MBBS, FRCPA Marcus Wagstaff, MBBS, PhD, FRACS Thoracic Outlet Syndrome Following Breast Implant Rupture Plastic and Reconstructive Surgery, Global Open |
author_facet |
Raakhi Mistry, MBChB Yugesh Caplash, MBBS, FRACS Pratyush Giri, MBBS, FRACP, FRCPA Daniel Kearney, MBBS, FRCPA Marcus Wagstaff, MBBS, PhD, FRACS |
author_sort |
Raakhi Mistry, MBChB |
title |
Thoracic Outlet Syndrome Following Breast Implant Rupture |
title_short |
Thoracic Outlet Syndrome Following Breast Implant Rupture |
title_full |
Thoracic Outlet Syndrome Following Breast Implant Rupture |
title_fullStr |
Thoracic Outlet Syndrome Following Breast Implant Rupture |
title_full_unstemmed |
Thoracic Outlet Syndrome Following Breast Implant Rupture |
title_sort |
thoracic outlet syndrome following breast implant rupture |
publisher |
Wolters Kluwer |
series |
Plastic and Reconstructive Surgery, Global Open |
issn |
2169-7574 |
publishDate |
2015-03-01 |
description |
Summary: We present a patient with bilateral breast implant rupture who developed severe locoregional silicone granulomatous lymphadenopathy. Poly Implant Prothese silicone implants had been used for bilateral breast augmentation 5 years prior. Extracapsular implant rupture and bilateral axillary lymphadenopathy indicated explantation, capsulectomy, and selective lymph node excision. Histology demonstrated silicone lymphadenopathy with no evidence of malignancy. Over the subsequent 12 months, she developed progressive locoregional lymphadenopathy involving bilateral cervical, axillary, and internal mammary groups, resulting in bilateral thoracic outlet syndrome. We report the unusual presentation, progression, and the ultimate surgical management of this patient. |
url |
http://journals.lww.com/prsgo/Fulltext/2015/03000/Article.17.aspx |
work_keys_str_mv |
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