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Massive pulmonary thromboembolism combined with transient thyrotoxicosis in an 18 year old girl
BACKGROUND: Pulmonary thromboembolism (PTE) is thought to usually stem from deep vein thrombosis (DVT). However, evidence of DVT could not be found in many cases. Furthermore, transient thyrotoxicosis is a rare but potentially life–threatening emergency involving a systemic hypercoagulable state. We...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7461343/ https://www.ncbi.nlm.nih.gov/pubmed/32884835 http://dx.doi.org/10.1186/s40885-020-00150-2 |
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author | Kim, Tong-Yoon Ihm, Sang-Hyun Roh, Ji Woong Lim, Sungmin Park, Chan-Seok Kim, Hee-Yeol |
author_facet | Kim, Tong-Yoon Ihm, Sang-Hyun Roh, Ji Woong Lim, Sungmin Park, Chan-Seok Kim, Hee-Yeol |
author_sort | Kim, Tong-Yoon |
collection | PubMed |
description | BACKGROUND: Pulmonary thromboembolism (PTE) is thought to usually stem from deep vein thrombosis (DVT). However, evidence of DVT could not be found in many cases. Furthermore, transient thyrotoxicosis is a rare but potentially life–threatening emergency involving a systemic hypercoagulable state. We report on an 18 year-old-girl with transient thyrotoxicosis with massive PTE without DVT. CASE PRESENTATION: An 18-year-old girl was admitted to the hospital with syncope. Patient had no history of trauma, any known underlying disease or oral contraceptives use. Chest computed tomography (CT) showed massive PTE in both central pulmonary arteries and diffuse goiter. However, a low extremity Doppler sonogram did not detect DVT. To manage the PTE, we administered low molecular weight heparin. On the other hands, thyroid function test indicated a state of thyrotoxicosis. In addition, patient had a partial protein S deficiency but no other immunologic abnormality. Therefore, the patient was diagnosed with massive PTE, thyrotoxicosis, and partial protein S deficiency. Patient was discharged with oral warfarin and methimazole. A follow-up echocardiogram obtained 3 months after anticoagulation therapy demonstrated normal dimensions and systolic function. After thyrotoxicosis was treated with methimazole for a month, a euthyroid state was achieved and the goiter decreased to a normal size. The methimazole was gradually tapered off and stopped at 4 months. At a 6-month follow up visit, PTE and pulmonary hypertension had disappeared but the patient still had a partial protein S deficiency. We decided to stop all medication with careful monitoring. During a 4-year follow-up period after the episode, she was asymptomatic without any evidence of recurrent systemic thromboembolism or hyperthyroidism. CONCLUSIONS: Early recognition and appropriate treatment of PTE combined with transient thyrotoxicosis were vital to preventing other complications. |
format | Online Article Text |
id | pubmed-7461343 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-74613432020-09-02 Massive pulmonary thromboembolism combined with transient thyrotoxicosis in an 18 year old girl Kim, Tong-Yoon Ihm, Sang-Hyun Roh, Ji Woong Lim, Sungmin Park, Chan-Seok Kim, Hee-Yeol Clin Hypertens Case Report BACKGROUND: Pulmonary thromboembolism (PTE) is thought to usually stem from deep vein thrombosis (DVT). However, evidence of DVT could not be found in many cases. Furthermore, transient thyrotoxicosis is a rare but potentially life–threatening emergency involving a systemic hypercoagulable state. We report on an 18 year-old-girl with transient thyrotoxicosis with massive PTE without DVT. CASE PRESENTATION: An 18-year-old girl was admitted to the hospital with syncope. Patient had no history of trauma, any known underlying disease or oral contraceptives use. Chest computed tomography (CT) showed massive PTE in both central pulmonary arteries and diffuse goiter. However, a low extremity Doppler sonogram did not detect DVT. To manage the PTE, we administered low molecular weight heparin. On the other hands, thyroid function test indicated a state of thyrotoxicosis. In addition, patient had a partial protein S deficiency but no other immunologic abnormality. Therefore, the patient was diagnosed with massive PTE, thyrotoxicosis, and partial protein S deficiency. Patient was discharged with oral warfarin and methimazole. A follow-up echocardiogram obtained 3 months after anticoagulation therapy demonstrated normal dimensions and systolic function. After thyrotoxicosis was treated with methimazole for a month, a euthyroid state was achieved and the goiter decreased to a normal size. The methimazole was gradually tapered off and stopped at 4 months. At a 6-month follow up visit, PTE and pulmonary hypertension had disappeared but the patient still had a partial protein S deficiency. We decided to stop all medication with careful monitoring. During a 4-year follow-up period after the episode, she was asymptomatic without any evidence of recurrent systemic thromboembolism or hyperthyroidism. CONCLUSIONS: Early recognition and appropriate treatment of PTE combined with transient thyrotoxicosis were vital to preventing other complications. BioMed Central 2020-09-01 /pmc/articles/PMC7461343/ /pubmed/32884835 http://dx.doi.org/10.1186/s40885-020-00150-2 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data. |
spellingShingle | Case Report Kim, Tong-Yoon Ihm, Sang-Hyun Roh, Ji Woong Lim, Sungmin Park, Chan-Seok Kim, Hee-Yeol Massive pulmonary thromboembolism combined with transient thyrotoxicosis in an 18 year old girl |
title | Massive pulmonary thromboembolism combined with transient thyrotoxicosis in an 18 year old girl |
title_full | Massive pulmonary thromboembolism combined with transient thyrotoxicosis in an 18 year old girl |
title_fullStr | Massive pulmonary thromboembolism combined with transient thyrotoxicosis in an 18 year old girl |
title_full_unstemmed | Massive pulmonary thromboembolism combined with transient thyrotoxicosis in an 18 year old girl |
title_short | Massive pulmonary thromboembolism combined with transient thyrotoxicosis in an 18 year old girl |
title_sort | massive pulmonary thromboembolism combined with transient thyrotoxicosis in an 18 year old girl |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7461343/ https://www.ncbi.nlm.nih.gov/pubmed/32884835 http://dx.doi.org/10.1186/s40885-020-00150-2 |
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