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Thymoma Causing Bilateral Upper Extremity Deep Vein Thrombosis

A 38-year-old African American male presented with progressive pain, swelling, numbness, and warmth of the left upper extremity ten days before admission. A chest computerized tomography scan showed a large 8.3 cm × 6.1 cm x 9.9 cm anterior mediastinal mass with compression of the left brachiocephal...

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Autores principales: Bui, Hoang, Helms, Jessica L., Sierra-Hoffman, Miguel, Stevens, Mark L., Deliz-Aguirre, Rafael, Castro-Lainez, Miriams T., Deliz, Rafael J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7152697/
https://www.ncbi.nlm.nih.gov/pubmed/32300521
http://dx.doi.org/10.1016/j.rmcr.2020.101049
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author Bui, Hoang
Helms, Jessica L.
Sierra-Hoffman, Miguel
Stevens, Mark L.
Deliz-Aguirre, Rafael
Castro-Lainez, Miriams T.
Deliz, Rafael J.
author_facet Bui, Hoang
Helms, Jessica L.
Sierra-Hoffman, Miguel
Stevens, Mark L.
Deliz-Aguirre, Rafael
Castro-Lainez, Miriams T.
Deliz, Rafael J.
author_sort Bui, Hoang
collection PubMed
description A 38-year-old African American male presented with progressive pain, swelling, numbness, and warmth of the left upper extremity ten days before admission. A chest computerized tomography scan showed a large 8.3 cm × 6.1 cm x 9.9 cm anterior mediastinal mass with compression of the left brachiocephalic vein and superior vena cava. A venous doppler showed multiple occlusive venous thrombi in bilateral upper extremities, including the bilateral internal jugular and subclavian veins, as well as the left subclavian, axillary, cephalic, brachial and median cubital veins. Further laboratory workup came positive for acetylcholine receptor binding antibody suggesting myasthenia gravis, but the patient was asymptomatic for myasthenia gravis. A percutaneous core CT guided biopsy pathology resulted in a predominant T-cell population CD5 positive with few B cells; the immunophenotypic features suggested Type B2 thymoma. To the best of our knowledge, this case is the only reported thymoma presenting with bilateral deep vein thrombosis of the upper extremities. The deep vein thrombosis therapy was enoxaparin 1mg/kg subcutaneously every 12 hours and dexamethasone 4mg intravenously every 4 hours as an anti-inflammatory drug for thymoma related compression of the mediastinum. The patient was referred to a tertiary oncological medical center for a total thymectomy, chemotherapy, and adjuvant radiotherapy.
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spelling pubmed-71526972020-04-16 Thymoma Causing Bilateral Upper Extremity Deep Vein Thrombosis Bui, Hoang Helms, Jessica L. Sierra-Hoffman, Miguel Stevens, Mark L. Deliz-Aguirre, Rafael Castro-Lainez, Miriams T. Deliz, Rafael J. Respir Med Case Rep Case Report A 38-year-old African American male presented with progressive pain, swelling, numbness, and warmth of the left upper extremity ten days before admission. A chest computerized tomography scan showed a large 8.3 cm × 6.1 cm x 9.9 cm anterior mediastinal mass with compression of the left brachiocephalic vein and superior vena cava. A venous doppler showed multiple occlusive venous thrombi in bilateral upper extremities, including the bilateral internal jugular and subclavian veins, as well as the left subclavian, axillary, cephalic, brachial and median cubital veins. Further laboratory workup came positive for acetylcholine receptor binding antibody suggesting myasthenia gravis, but the patient was asymptomatic for myasthenia gravis. A percutaneous core CT guided biopsy pathology resulted in a predominant T-cell population CD5 positive with few B cells; the immunophenotypic features suggested Type B2 thymoma. To the best of our knowledge, this case is the only reported thymoma presenting with bilateral deep vein thrombosis of the upper extremities. The deep vein thrombosis therapy was enoxaparin 1mg/kg subcutaneously every 12 hours and dexamethasone 4mg intravenously every 4 hours as an anti-inflammatory drug for thymoma related compression of the mediastinum. The patient was referred to a tertiary oncological medical center for a total thymectomy, chemotherapy, and adjuvant radiotherapy. Elsevier 2020-04-03 /pmc/articles/PMC7152697/ /pubmed/32300521 http://dx.doi.org/10.1016/j.rmcr.2020.101049 Text en © 2020 The Authors http://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
Bui, Hoang
Helms, Jessica L.
Sierra-Hoffman, Miguel
Stevens, Mark L.
Deliz-Aguirre, Rafael
Castro-Lainez, Miriams T.
Deliz, Rafael J.
Thymoma Causing Bilateral Upper Extremity Deep Vein Thrombosis
title Thymoma Causing Bilateral Upper Extremity Deep Vein Thrombosis
title_full Thymoma Causing Bilateral Upper Extremity Deep Vein Thrombosis
title_fullStr Thymoma Causing Bilateral Upper Extremity Deep Vein Thrombosis
title_full_unstemmed Thymoma Causing Bilateral Upper Extremity Deep Vein Thrombosis
title_short Thymoma Causing Bilateral Upper Extremity Deep Vein Thrombosis
title_sort thymoma causing bilateral upper extremity deep vein thrombosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7152697/
https://www.ncbi.nlm.nih.gov/pubmed/32300521
http://dx.doi.org/10.1016/j.rmcr.2020.101049
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