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A 7-year-old boy with recurrent cyanosis and tachypnea: A case report
BACKGROUND: Brain tumors are the most common solid tumors in children and comprise 25% of all malignancies in children. Common presentations include headache, nausea and vomiting, gait abnormality, papilledema, and epileptic seizure; however, some symptoms can be very insidious, with atypical and mi...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Baishideng Publishing Group Inc
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9297426/ https://www.ncbi.nlm.nih.gov/pubmed/36051109 http://dx.doi.org/10.12998/wjcc.v10.i20.6974 |
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author | Li, Shu Chen, Li-Na Zhong, Lin |
author_facet | Li, Shu Chen, Li-Na Zhong, Lin |
author_sort | Li, Shu |
collection | PubMed |
description | BACKGROUND: Brain tumors are the most common solid tumors in children and comprise 25% of all malignancies in children. Common presentations include headache, nausea and vomiting, gait abnormality, papilledema, and epileptic seizure; however, some symptoms can be very insidious, with atypical and misleading manifestations. CASE SUMMARY: Here, we report a 7-year-old boy who presented with recurrent cyanosis and tachypnea after exercise for 2 years. His body mass index was 26.43 kg/m(2). Hepatosplenomegaly, blood gas analysis, biochemical parameters, chest computed tomography scan, and echocardiograph suggested type II respiratory failure, pulmonary heart disease, and mild liver injury. Non-invasive breathing support, antibiotics, and anti-heart failure therapy were given. The patient’s pulse oxygen saturation increased to over 95% when he was awake but dropped to 50%-60%, accompanied by cyanosis, during sleep while receiving high-flow nasal cannula oxygen. Sleep-related breathing disorder was suspected. In the intensive care unit, however, polysomnography was unavailable. Brain magnetic resonance imaging revealed a space-occupying (cerebellum and brainstem) lesion, which was later confirmed to be pleomorphic xanthoastrocytoma by surgery and histopathology by tissue biopsy. CONCLUSION: When treating patients with cyanosis and tachypnea, a broad differential diagnosis should be considered, including brain tumor. |
format | Online Article Text |
id | pubmed-9297426 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-92974262022-08-31 A 7-year-old boy with recurrent cyanosis and tachypnea: A case report Li, Shu Chen, Li-Na Zhong, Lin World J Clin Cases Case Report BACKGROUND: Brain tumors are the most common solid tumors in children and comprise 25% of all malignancies in children. Common presentations include headache, nausea and vomiting, gait abnormality, papilledema, and epileptic seizure; however, some symptoms can be very insidious, with atypical and misleading manifestations. CASE SUMMARY: Here, we report a 7-year-old boy who presented with recurrent cyanosis and tachypnea after exercise for 2 years. His body mass index was 26.43 kg/m(2). Hepatosplenomegaly, blood gas analysis, biochemical parameters, chest computed tomography scan, and echocardiograph suggested type II respiratory failure, pulmonary heart disease, and mild liver injury. Non-invasive breathing support, antibiotics, and anti-heart failure therapy were given. The patient’s pulse oxygen saturation increased to over 95% when he was awake but dropped to 50%-60%, accompanied by cyanosis, during sleep while receiving high-flow nasal cannula oxygen. Sleep-related breathing disorder was suspected. In the intensive care unit, however, polysomnography was unavailable. Brain magnetic resonance imaging revealed a space-occupying (cerebellum and brainstem) lesion, which was later confirmed to be pleomorphic xanthoastrocytoma by surgery and histopathology by tissue biopsy. CONCLUSION: When treating patients with cyanosis and tachypnea, a broad differential diagnosis should be considered, including brain tumor. Baishideng Publishing Group Inc 2022-07-16 2022-07-16 /pmc/articles/PMC9297426/ /pubmed/36051109 http://dx.doi.org/10.12998/wjcc.v10.i20.6974 Text en ©The Author(s) 2022. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/ |
spellingShingle | Case Report Li, Shu Chen, Li-Na Zhong, Lin A 7-year-old boy with recurrent cyanosis and tachypnea: A case report |
title | A 7-year-old boy with recurrent cyanosis and tachypnea: A case report |
title_full | A 7-year-old boy with recurrent cyanosis and tachypnea: A case report |
title_fullStr | A 7-year-old boy with recurrent cyanosis and tachypnea: A case report |
title_full_unstemmed | A 7-year-old boy with recurrent cyanosis and tachypnea: A case report |
title_short | A 7-year-old boy with recurrent cyanosis and tachypnea: A case report |
title_sort | 7-year-old boy with recurrent cyanosis and tachypnea: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9297426/ https://www.ncbi.nlm.nih.gov/pubmed/36051109 http://dx.doi.org/10.12998/wjcc.v10.i20.6974 |
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