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Paget-von Schroetter syndrome: Case report
INTRODUCTION: Paget-von Schroetter Syndrome is a rare condition, which refers to primary venous thrombosis of the subclavian-axillary bed. It is related to vigorous activities involving the upper limbs, presenting pain, edema and muscle swelling. Its diagnosis involves, besides the clinical suspicio...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8524747/ https://www.ncbi.nlm.nih.gov/pubmed/34666254 http://dx.doi.org/10.1016/j.ijscr.2021.106509 |
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author | de Siqueira Filho, Josias Torres de Paula, Railane Lima Régis, Arthur César Albuquerque Figueiredo, Alberto Rubin von Mühlen, Bruno Peres, João Victor Fuzeta |
author_facet | de Siqueira Filho, Josias Torres de Paula, Railane Lima Régis, Arthur César Albuquerque Figueiredo, Alberto Rubin von Mühlen, Bruno Peres, João Victor Fuzeta |
author_sort | de Siqueira Filho, Josias Torres |
collection | PubMed |
description | INTRODUCTION: Paget-von Schroetter Syndrome is a rare condition, which refers to primary venous thrombosis of the subclavian-axillary bed. It is related to vigorous activities involving the upper limbs, presenting pain, edema and muscle swelling. Its diagnosis involves, besides the clinical suspicion, Doppler ultrasonography and should be performed early to ensure immediate treatment. The therapy is initially made with anticoagulation, but thrombolysis, decompression surgery, venolysis and venoplasty should be considered, which can lead to a better prognosis and lower risk of complications. CASE REPORT: This article refers to a report of a male patient, with a history of physical activity, who developed thrombosis in the left upper limb and evolved, after anticoagulant treatment, to post-thrombotic syndrome. DISCUSSION: Paget-von Schroetter syndrome can be asymptomatic, but common features include hyperemia, edema, heaviness and pain in the affected arm, usually 24 h after the initial event and may be accompanied by low fever. In diagnostic investigation, imaging exam is essential. Early diagnosis of the syndrome allows the early start of treatment, leading to better results and prognosis. CONCLUSION: Therefore, this study has the goal of making the diagnosis more effective and improves the clinical-surgical management, from the increase in the level of medical professionals' suspicion regarding the disease. |
format | Online Article Text |
id | pubmed-8524747 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-85247472021-10-25 Paget-von Schroetter syndrome: Case report de Siqueira Filho, Josias Torres de Paula, Railane Lima Régis, Arthur César Albuquerque Figueiredo, Alberto Rubin von Mühlen, Bruno Peres, João Victor Fuzeta Int J Surg Case Rep Case Report INTRODUCTION: Paget-von Schroetter Syndrome is a rare condition, which refers to primary venous thrombosis of the subclavian-axillary bed. It is related to vigorous activities involving the upper limbs, presenting pain, edema and muscle swelling. Its diagnosis involves, besides the clinical suspicion, Doppler ultrasonography and should be performed early to ensure immediate treatment. The therapy is initially made with anticoagulation, but thrombolysis, decompression surgery, venolysis and venoplasty should be considered, which can lead to a better prognosis and lower risk of complications. CASE REPORT: This article refers to a report of a male patient, with a history of physical activity, who developed thrombosis in the left upper limb and evolved, after anticoagulant treatment, to post-thrombotic syndrome. DISCUSSION: Paget-von Schroetter syndrome can be asymptomatic, but common features include hyperemia, edema, heaviness and pain in the affected arm, usually 24 h after the initial event and may be accompanied by low fever. In diagnostic investigation, imaging exam is essential. Early diagnosis of the syndrome allows the early start of treatment, leading to better results and prognosis. CONCLUSION: Therefore, this study has the goal of making the diagnosis more effective and improves the clinical-surgical management, from the increase in the level of medical professionals' suspicion regarding the disease. Elsevier 2021-10-16 /pmc/articles/PMC8524747/ /pubmed/34666254 http://dx.doi.org/10.1016/j.ijscr.2021.106509 Text en © 2021 Published by Elsevier Ltd on behalf of IJS Publishing Group Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report de Siqueira Filho, Josias Torres de Paula, Railane Lima Régis, Arthur César Albuquerque Figueiredo, Alberto Rubin von Mühlen, Bruno Peres, João Victor Fuzeta Paget-von Schroetter syndrome: Case report |
title | Paget-von Schroetter syndrome: Case report |
title_full | Paget-von Schroetter syndrome: Case report |
title_fullStr | Paget-von Schroetter syndrome: Case report |
title_full_unstemmed | Paget-von Schroetter syndrome: Case report |
title_short | Paget-von Schroetter syndrome: Case report |
title_sort | paget-von schroetter syndrome: case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8524747/ https://www.ncbi.nlm.nih.gov/pubmed/34666254 http://dx.doi.org/10.1016/j.ijscr.2021.106509 |
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