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What do we know about Tietze’s syndrome?
Tietze’s syndrome is a benign, self-limiting arthropathy, without purulent character. The disease most often involves articulations: sternocostal, sternoclavicular, or costochondral joints. The characteristic symptoms are tenderness, pain and edema involving one of the aforementioned joints on one s...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6180027/ https://www.ncbi.nlm.nih.gov/pubmed/30310397 http://dx.doi.org/10.5114/kitp.2018.78443 |
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author | Rokicki, Wojciech Rokicki, Marek Rydel, Mateusz |
author_facet | Rokicki, Wojciech Rokicki, Marek Rydel, Mateusz |
author_sort | Rokicki, Wojciech |
collection | PubMed |
description | Tietze’s syndrome is a benign, self-limiting arthropathy, without purulent character. The disease most often involves articulations: sternocostal, sternoclavicular, or costochondral joints. The characteristic symptoms are tenderness, pain and edema involving one of the aforementioned joints on one side. Diagnosis of Tietze’s syndrome is based on physical examination (increase of palpation tenderness in the affected joint), laboratory tests (increase of inflammatory parameters) and imaging studies (USG, MRI). Differential diagnosis of Tietze’s syndrome is based on exclusion of costal cartilage inflammation, coronary syndrome and inflammatory changes in the lung and pleura. Most commonly the treatment is conservative, in resistant cases surgical. |
format | Online Article Text |
id | pubmed-6180027 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Termedia Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-61800272018-10-11 What do we know about Tietze’s syndrome? Rokicki, Wojciech Rokicki, Marek Rydel, Mateusz Kardiochir Torakochirurgia Pol Review Paper Tietze’s syndrome is a benign, self-limiting arthropathy, without purulent character. The disease most often involves articulations: sternocostal, sternoclavicular, or costochondral joints. The characteristic symptoms are tenderness, pain and edema involving one of the aforementioned joints on one side. Diagnosis of Tietze’s syndrome is based on physical examination (increase of palpation tenderness in the affected joint), laboratory tests (increase of inflammatory parameters) and imaging studies (USG, MRI). Differential diagnosis of Tietze’s syndrome is based on exclusion of costal cartilage inflammation, coronary syndrome and inflammatory changes in the lung and pleura. Most commonly the treatment is conservative, in resistant cases surgical. Termedia Publishing House 2018-09-24 2018-09 /pmc/articles/PMC6180027/ /pubmed/30310397 http://dx.doi.org/10.5114/kitp.2018.78443 Text en Copyright: © 2018 Polish Society of Cardiothoracic Surgeons (Polskie Towarzystwo KardioTorakochirurgów) and the editors of the Polish Journal of Cardio-Thoracic Surgery (Kardiochirurgia i Torakochirurgia Polska) http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license. |
spellingShingle | Review Paper Rokicki, Wojciech Rokicki, Marek Rydel, Mateusz What do we know about Tietze’s syndrome? |
title | What do we know about Tietze’s syndrome? |
title_full | What do we know about Tietze’s syndrome? |
title_fullStr | What do we know about Tietze’s syndrome? |
title_full_unstemmed | What do we know about Tietze’s syndrome? |
title_short | What do we know about Tietze’s syndrome? |
title_sort | what do we know about tietze’s syndrome? |
topic | Review Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6180027/ https://www.ncbi.nlm.nih.gov/pubmed/30310397 http://dx.doi.org/10.5114/kitp.2018.78443 |
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