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Pulmonary Fibrosis Secondary to FOLFOX Chemotherapy: A Case Report
A 54-year-old female presented with a 2-week history of increasing shortness of breath and fever. She had a history of a poorly differentiated sigmoid adenocarcinoma for which she underwent an anterior resection 6 months prior to admission, followed by 12 cycles of adjuvant FOLFOX chemotherapy. The...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
S. Karger AG
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4224254/ https://www.ncbi.nlm.nih.gov/pubmed/25408660 http://dx.doi.org/10.1159/000368185 |
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author | Soon, Wai Cheong West, Kate Gibeon, David Bowen, Elizabeth Frances |
author_facet | Soon, Wai Cheong West, Kate Gibeon, David Bowen, Elizabeth Frances |
author_sort | Soon, Wai Cheong |
collection | PubMed |
description | A 54-year-old female presented with a 2-week history of increasing shortness of breath and fever. She had a history of a poorly differentiated sigmoid adenocarcinoma for which she underwent an anterior resection 6 months prior to admission, followed by 12 cycles of adjuvant FOLFOX chemotherapy. The patient was treated for a severe community-acquired pneumonia; however, she remained hypoxic. A chest CT revealed extensive right-sided fibrotic changes, tractional dilatation of the airways and ground glass density, which had developed since a staging CT scan performed 2 months previously. Although her symptoms improved with steroid therapy, repeat imaging revealed that right hydropneumothorax had developed, and this required the insertion of a chest drain. Following its successful removal, the patient continues to improve clinically and radiographically. The rapid onset and nature of these changes is consistent with a drug-induced fibrotic lung disease secondary to FOLFOX chemotherapy. The phenomenon is underreported and yet, it is relatively common: it occurs in approximately 10% of patients who are treated with antineoplastic agents, although information specifically relating to FOLFOX-induced pulmonary toxicity is limited. It is associated with significant morbidity and mortality, but is often hard to differentiate from other lung conditions, making the diagnosis a challenge. Pulmonary toxicity is an important complication associated with antineoplastic agents. It should be considered in any patient on a chemotherapeutic regimen who presents with dyspnoea and hypoxia in order to try to reduce the associated morbidity and mortality. |
format | Online Article Text |
id | pubmed-4224254 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | S. Karger AG |
record_format | MEDLINE/PubMed |
spelling | pubmed-42242542014-11-18 Pulmonary Fibrosis Secondary to FOLFOX Chemotherapy: A Case Report Soon, Wai Cheong West, Kate Gibeon, David Bowen, Elizabeth Frances Case Rep Oncol Published online: September, 2014 A 54-year-old female presented with a 2-week history of increasing shortness of breath and fever. She had a history of a poorly differentiated sigmoid adenocarcinoma for which she underwent an anterior resection 6 months prior to admission, followed by 12 cycles of adjuvant FOLFOX chemotherapy. The patient was treated for a severe community-acquired pneumonia; however, she remained hypoxic. A chest CT revealed extensive right-sided fibrotic changes, tractional dilatation of the airways and ground glass density, which had developed since a staging CT scan performed 2 months previously. Although her symptoms improved with steroid therapy, repeat imaging revealed that right hydropneumothorax had developed, and this required the insertion of a chest drain. Following its successful removal, the patient continues to improve clinically and radiographically. The rapid onset and nature of these changes is consistent with a drug-induced fibrotic lung disease secondary to FOLFOX chemotherapy. The phenomenon is underreported and yet, it is relatively common: it occurs in approximately 10% of patients who are treated with antineoplastic agents, although information specifically relating to FOLFOX-induced pulmonary toxicity is limited. It is associated with significant morbidity and mortality, but is often hard to differentiate from other lung conditions, making the diagnosis a challenge. Pulmonary toxicity is an important complication associated with antineoplastic agents. It should be considered in any patient on a chemotherapeutic regimen who presents with dyspnoea and hypoxia in order to try to reduce the associated morbidity and mortality. S. Karger AG 2014-09-24 /pmc/articles/PMC4224254/ /pubmed/25408660 http://dx.doi.org/10.1159/000368185 Text en Copyright © 2014 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article licensed under the terms of the Creative Commons Attribution-NonCommercial 3.0 Unported license (CC BY-NC) (www.karger.com/OA-license), applicable to the online version of the article only. Users may download, print and share this work on the Internet for noncommercial purposes only, provided the original work is properly cited, and a link to the original work on http://www.karger.com and the terms of this license are included in any shared versions. |
spellingShingle | Published online: September, 2014 Soon, Wai Cheong West, Kate Gibeon, David Bowen, Elizabeth Frances Pulmonary Fibrosis Secondary to FOLFOX Chemotherapy: A Case Report |
title | Pulmonary Fibrosis Secondary to FOLFOX Chemotherapy: A Case Report |
title_full | Pulmonary Fibrosis Secondary to FOLFOX Chemotherapy: A Case Report |
title_fullStr | Pulmonary Fibrosis Secondary to FOLFOX Chemotherapy: A Case Report |
title_full_unstemmed | Pulmonary Fibrosis Secondary to FOLFOX Chemotherapy: A Case Report |
title_short | Pulmonary Fibrosis Secondary to FOLFOX Chemotherapy: A Case Report |
title_sort | pulmonary fibrosis secondary to folfox chemotherapy: a case report |
topic | Published online: September, 2014 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4224254/ https://www.ncbi.nlm.nih.gov/pubmed/25408660 http://dx.doi.org/10.1159/000368185 |
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