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A rare and highly malignant Stwart-Treves syndrome case after breast cancer surgery: a case report
BACKGROUND: Stewart-Treves syndrome (STS) is a lymphatic sarcoma secondary to chronic lymphedema of the extremities. Most STS patients have a history of breast cancer and have undergone radical mastectomy and postoperative radiation and chemotherapy. It usually occurs 11 to 12 years after surgery, a...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9346214/ https://www.ncbi.nlm.nih.gov/pubmed/35935569 http://dx.doi.org/10.21037/gs-22-344 |
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author | Lu, Hongrui Yang, Xiaodong Zhu, Ziguan Zhu, Xiuming Guo, Enqi Yuan, Rong |
author_facet | Lu, Hongrui Yang, Xiaodong Zhu, Ziguan Zhu, Xiuming Guo, Enqi Yuan, Rong |
author_sort | Lu, Hongrui |
collection | PubMed |
description | BACKGROUND: Stewart-Treves syndrome (STS) is a lymphatic sarcoma secondary to chronic lymphedema of the extremities. Most STS patients have a history of breast cancer and have undergone radical mastectomy and postoperative radiation and chemotherapy. It usually occurs 11 to 12 years after surgery, and about 0.45% of patients are estimated to have the disease. The characteristics of STS include that it is clinically relatively rare, has a high degree of malignancy, can spread easily in the absence of timely treatment, and has low survival rate. Herein, we report a case of STS which developed 13 years after breast cancer-related lymphoedema (BCRL). It allows doctors to recognize and detect the disease earlier. CASE DESCRIPTION: A 74-year-old woman had undergone modified radical mastectomy 13 years ago for invasive ductal breast cancer in her left breast. After multiple rounds of postoperative chemoradiotherapy, multiple purple lesions were found in the left upper limb during physical examination in April 2021. The lesions spread rapidly and were varied in size. An immediate skin biopsy reported the lesions as STS. The patient was diagnosed with lymphangiosarcoma with metastasis (STS). The surgical method was shoulder joint amputation, chest wall resection, and local flap transfer. After surgery, the patient underwent 6 rounds of paclitaxel 300 mg + carboplatin 300 mg chemotherapy. After chemotherapy, the patient’s wound healed and the suspected metastasis disappeared. At the time of writing, she has survived for more than 13 months, and her quality of life has improved significantly, to the satisfaction of the patient and her family. The patient is able to eat normally and lead a normal life with some assistance, without significant weight loss. CONCLUSIONS: Although rare, STS is a serious invasive complication of breast cancer surgery. To increase their relative survival time, patients with BCRL need to identify and thoroughly investigate rapidly progressing skin lesions, and undergo timely surgery. |
format | Online Article Text |
id | pubmed-9346214 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-93462142022-08-04 A rare and highly malignant Stwart-Treves syndrome case after breast cancer surgery: a case report Lu, Hongrui Yang, Xiaodong Zhu, Ziguan Zhu, Xiuming Guo, Enqi Yuan, Rong Gland Surg Case Report BACKGROUND: Stewart-Treves syndrome (STS) is a lymphatic sarcoma secondary to chronic lymphedema of the extremities. Most STS patients have a history of breast cancer and have undergone radical mastectomy and postoperative radiation and chemotherapy. It usually occurs 11 to 12 years after surgery, and about 0.45% of patients are estimated to have the disease. The characteristics of STS include that it is clinically relatively rare, has a high degree of malignancy, can spread easily in the absence of timely treatment, and has low survival rate. Herein, we report a case of STS which developed 13 years after breast cancer-related lymphoedema (BCRL). It allows doctors to recognize and detect the disease earlier. CASE DESCRIPTION: A 74-year-old woman had undergone modified radical mastectomy 13 years ago for invasive ductal breast cancer in her left breast. After multiple rounds of postoperative chemoradiotherapy, multiple purple lesions were found in the left upper limb during physical examination in April 2021. The lesions spread rapidly and were varied in size. An immediate skin biopsy reported the lesions as STS. The patient was diagnosed with lymphangiosarcoma with metastasis (STS). The surgical method was shoulder joint amputation, chest wall resection, and local flap transfer. After surgery, the patient underwent 6 rounds of paclitaxel 300 mg + carboplatin 300 mg chemotherapy. After chemotherapy, the patient’s wound healed and the suspected metastasis disappeared. At the time of writing, she has survived for more than 13 months, and her quality of life has improved significantly, to the satisfaction of the patient and her family. The patient is able to eat normally and lead a normal life with some assistance, without significant weight loss. CONCLUSIONS: Although rare, STS is a serious invasive complication of breast cancer surgery. To increase their relative survival time, patients with BCRL need to identify and thoroughly investigate rapidly progressing skin lesions, and undergo timely surgery. AME Publishing Company 2022-07 /pmc/articles/PMC9346214/ /pubmed/35935569 http://dx.doi.org/10.21037/gs-22-344 Text en 2022 Gland Surgery. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Case Report Lu, Hongrui Yang, Xiaodong Zhu, Ziguan Zhu, Xiuming Guo, Enqi Yuan, Rong A rare and highly malignant Stwart-Treves syndrome case after breast cancer surgery: a case report |
title | A rare and highly malignant Stwart-Treves syndrome case after breast cancer surgery: a case report |
title_full | A rare and highly malignant Stwart-Treves syndrome case after breast cancer surgery: a case report |
title_fullStr | A rare and highly malignant Stwart-Treves syndrome case after breast cancer surgery: a case report |
title_full_unstemmed | A rare and highly malignant Stwart-Treves syndrome case after breast cancer surgery: a case report |
title_short | A rare and highly malignant Stwart-Treves syndrome case after breast cancer surgery: a case report |
title_sort | rare and highly malignant stwart-treves syndrome case after breast cancer surgery: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9346214/ https://www.ncbi.nlm.nih.gov/pubmed/35935569 http://dx.doi.org/10.21037/gs-22-344 |
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