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Spontaneous Pneumomediastinum: A Rare Disease Associated with Chest Pain in Adolescents
PURPOSE: Spontaneous pneumomediastinum (SPM) is a rare entity, with only a few cases reported, especially in adolescents. We aimed to analyze the clinical characteristics of SPM in adolescents and the diagnostic implications of computed tomography (CT) and esophagography therein. MATERIALS AND METHO...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Yonsei University College of Medicine
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4541679/ https://www.ncbi.nlm.nih.gov/pubmed/26256992 http://dx.doi.org/10.3349/ymj.2015.56.5.1437 |
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author | Kim, Sung Hoon Huh, June Song, Jinyoung Kang, I-Seok |
author_facet | Kim, Sung Hoon Huh, June Song, Jinyoung Kang, I-Seok |
author_sort | Kim, Sung Hoon |
collection | PubMed |
description | PURPOSE: Spontaneous pneumomediastinum (SPM) is a rare entity, with only a few cases reported, especially in adolescents. We aimed to analyze the clinical characteristics of SPM in adolescents and the diagnostic implications of computed tomography (CT) and esophagography therein. MATERIALS AND METHODS: This retrospective descriptive study was conducted as a review of medical records of 416 adolescents (10-18 years of age) with chest pain from March 2005 to June 2013. Information on clinical presentation, methods of diagnosis, hospital stay, and outcomes were collected and analyzed. RESULTS: Among adolescents complaining of chest pain, 11 patients had SPM (11/416, 2.64%). All patients presented with pleuritic chest pain, and 54.5% reported neck pain as the most common associated complaint. Clinical findings were nonspecific, and initial chest X-ray assessment was diagnostic only in three of 11 patients. However, reassessment of chest X-ray revealed diagnostic findings of SPM in five of the remaining eight patients. CT was diagnostic in all patients, while esophagography and echocardiogram were uninformative. Symptomatic improvement was noted within 2.45±1.2 hours (range, 0.5 to 4) after supportive care; mean hospital stay was 4.54±0.99 days (range, 2 to 6). No recurrence was observed. CONCLUSION: SPM is a rare disease that should be considered in adolescent patients with pleuritic chest pain. Careful reading of initial chest X-rays is important to avoiding further unnecessary investigations. SPM is self-limited and treatment is supportive; nevertheless, if there are no indications of esophageal rupture, urgent esophagography is not recommended. |
format | Online Article Text |
id | pubmed-4541679 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Yonsei University College of Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-45416792015-09-01 Spontaneous Pneumomediastinum: A Rare Disease Associated with Chest Pain in Adolescents Kim, Sung Hoon Huh, June Song, Jinyoung Kang, I-Seok Yonsei Med J Original Article PURPOSE: Spontaneous pneumomediastinum (SPM) is a rare entity, with only a few cases reported, especially in adolescents. We aimed to analyze the clinical characteristics of SPM in adolescents and the diagnostic implications of computed tomography (CT) and esophagography therein. MATERIALS AND METHODS: This retrospective descriptive study was conducted as a review of medical records of 416 adolescents (10-18 years of age) with chest pain from March 2005 to June 2013. Information on clinical presentation, methods of diagnosis, hospital stay, and outcomes were collected and analyzed. RESULTS: Among adolescents complaining of chest pain, 11 patients had SPM (11/416, 2.64%). All patients presented with pleuritic chest pain, and 54.5% reported neck pain as the most common associated complaint. Clinical findings were nonspecific, and initial chest X-ray assessment was diagnostic only in three of 11 patients. However, reassessment of chest X-ray revealed diagnostic findings of SPM in five of the remaining eight patients. CT was diagnostic in all patients, while esophagography and echocardiogram were uninformative. Symptomatic improvement was noted within 2.45±1.2 hours (range, 0.5 to 4) after supportive care; mean hospital stay was 4.54±0.99 days (range, 2 to 6). No recurrence was observed. CONCLUSION: SPM is a rare disease that should be considered in adolescent patients with pleuritic chest pain. Careful reading of initial chest X-rays is important to avoiding further unnecessary investigations. SPM is self-limited and treatment is supportive; nevertheless, if there are no indications of esophageal rupture, urgent esophagography is not recommended. Yonsei University College of Medicine 2015-09-01 2015-07-29 /pmc/articles/PMC4541679/ /pubmed/26256992 http://dx.doi.org/10.3349/ymj.2015.56.5.1437 Text en © Copyright: Yonsei University College of Medicine 2015 http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Kim, Sung Hoon Huh, June Song, Jinyoung Kang, I-Seok Spontaneous Pneumomediastinum: A Rare Disease Associated with Chest Pain in Adolescents |
title | Spontaneous Pneumomediastinum: A Rare Disease Associated with Chest Pain in Adolescents |
title_full | Spontaneous Pneumomediastinum: A Rare Disease Associated with Chest Pain in Adolescents |
title_fullStr | Spontaneous Pneumomediastinum: A Rare Disease Associated with Chest Pain in Adolescents |
title_full_unstemmed | Spontaneous Pneumomediastinum: A Rare Disease Associated with Chest Pain in Adolescents |
title_short | Spontaneous Pneumomediastinum: A Rare Disease Associated with Chest Pain in Adolescents |
title_sort | spontaneous pneumomediastinum: a rare disease associated with chest pain in adolescents |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4541679/ https://www.ncbi.nlm.nih.gov/pubmed/26256992 http://dx.doi.org/10.3349/ymj.2015.56.5.1437 |
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