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Paget-Schroetter syndrome in the absence of common predisposing factors: a case report

BACKGROUND: Paget-Schrotter Syndrome (PSS) also known as “effort thrombosis” is a form of primary thrombosis in the subclavian vein at the costoclavicular junction is usually seen in younger patients after repeated strenuous activity of the shoulders and arms. When occurring in younger patients, PSS...

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Autores principales: Ibrahim, Ramy, Dashkova, Irina, Williams, Myia, Kozikowski, Andrzej, Abrol, Neeraj, Gandhi, Anjula, Pekmezaris, Renee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5537934/
https://www.ncbi.nlm.nih.gov/pubmed/28781584
http://dx.doi.org/10.1186/s12959-017-0146-0
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author Ibrahim, Ramy
Dashkova, Irina
Williams, Myia
Kozikowski, Andrzej
Abrol, Neeraj
Gandhi, Anjula
Pekmezaris, Renee
author_facet Ibrahim, Ramy
Dashkova, Irina
Williams, Myia
Kozikowski, Andrzej
Abrol, Neeraj
Gandhi, Anjula
Pekmezaris, Renee
author_sort Ibrahim, Ramy
collection PubMed
description BACKGROUND: Paget-Schrotter Syndrome (PSS) also known as “effort thrombosis” is a form of primary thrombosis in the subclavian vein at the costoclavicular junction is usually seen in younger patients after repeated strenuous activity of the shoulders and arms. When occurring in younger patients, PSS presents itself with predisposing factors such as unilateral dull, aching pain in the shoulder or axilla and swelling of the arm and hand. CASE PRESENTATION: We report a rare case of unusual left axillo-subclavian vein thrombosis in absence of clear risk factors and a negative hypercoagulable workup in a 36-year-old Hispanic woman who presented with 2 days duration of left upper extremity pain and swelling after a week of heavy exercise in aerobic class. Very few documented cases of primary or spontaneous ASVT in absence of clear factors and in such anatomical location have been previously reported. The patient was started on strict precautions of left upper extremity immobilization, analgesics in the form of Tylenol 650 mg every 6 h for pain as well as cold compresses. Lovenox 90 mg subcutaneous twice daily (1 mg/kg BID) was started together with warfarin to keep INR 2–3. CONCLUSION: In addition to the unusual location in the left upper extremity in our case, the absence of common etiologic factors makes our case of Paget-Schroetter Syndrome a very unique one. Presently, there is a lack of guided management of rare conditions such as our case, or consensus among the sources. Physicians should be aware of this rare disease since untreated conditions may be debilitating for the patient and very costly especially if diagnosed with a delay.
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spelling pubmed-55379342017-08-04 Paget-Schroetter syndrome in the absence of common predisposing factors: a case report Ibrahim, Ramy Dashkova, Irina Williams, Myia Kozikowski, Andrzej Abrol, Neeraj Gandhi, Anjula Pekmezaris, Renee Thromb J Case Report BACKGROUND: Paget-Schrotter Syndrome (PSS) also known as “effort thrombosis” is a form of primary thrombosis in the subclavian vein at the costoclavicular junction is usually seen in younger patients after repeated strenuous activity of the shoulders and arms. When occurring in younger patients, PSS presents itself with predisposing factors such as unilateral dull, aching pain in the shoulder or axilla and swelling of the arm and hand. CASE PRESENTATION: We report a rare case of unusual left axillo-subclavian vein thrombosis in absence of clear risk factors and a negative hypercoagulable workup in a 36-year-old Hispanic woman who presented with 2 days duration of left upper extremity pain and swelling after a week of heavy exercise in aerobic class. Very few documented cases of primary or spontaneous ASVT in absence of clear factors and in such anatomical location have been previously reported. The patient was started on strict precautions of left upper extremity immobilization, analgesics in the form of Tylenol 650 mg every 6 h for pain as well as cold compresses. Lovenox 90 mg subcutaneous twice daily (1 mg/kg BID) was started together with warfarin to keep INR 2–3. CONCLUSION: In addition to the unusual location in the left upper extremity in our case, the absence of common etiologic factors makes our case of Paget-Schroetter Syndrome a very unique one. Presently, there is a lack of guided management of rare conditions such as our case, or consensus among the sources. Physicians should be aware of this rare disease since untreated conditions may be debilitating for the patient and very costly especially if diagnosed with a delay. BioMed Central 2017-08-01 /pmc/articles/PMC5537934/ /pubmed/28781584 http://dx.doi.org/10.1186/s12959-017-0146-0 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Ibrahim, Ramy
Dashkova, Irina
Williams, Myia
Kozikowski, Andrzej
Abrol, Neeraj
Gandhi, Anjula
Pekmezaris, Renee
Paget-Schroetter syndrome in the absence of common predisposing factors: a case report
title Paget-Schroetter syndrome in the absence of common predisposing factors: a case report
title_full Paget-Schroetter syndrome in the absence of common predisposing factors: a case report
title_fullStr Paget-Schroetter syndrome in the absence of common predisposing factors: a case report
title_full_unstemmed Paget-Schroetter syndrome in the absence of common predisposing factors: a case report
title_short Paget-Schroetter syndrome in the absence of common predisposing factors: a case report
title_sort paget-schroetter syndrome in the absence of common predisposing factors: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5537934/
https://www.ncbi.nlm.nih.gov/pubmed/28781584
http://dx.doi.org/10.1186/s12959-017-0146-0
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