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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...

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Detalles Bibliográficos
Autores principales: Rokicki, Wojciech, Rokicki, Marek, Rydel, Mateusz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2018
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.
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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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