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Pneumatosis intestinalis and portal venous gas secondary to Gefitinib therapy for lung adenocarcinoma
BACKGROUND: Pneumatosis intestinalis (PI), defined as the presence of gas in the bowel wall, and portal venous gas (PVG) are relatively rare radiological findings. Although several chemotherapeutic agents and anti-vascular endothelial growth factor agents are reported to be associated with PI and PV...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3314573/ https://www.ncbi.nlm.nih.gov/pubmed/22405425 http://dx.doi.org/10.1186/1471-2407-12-87 |
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author | Lee, Joo Young Han, Hye-Suk Lim, Sung-Nam Shim, Young Kwang Choi, Yong Hyeok Lee, Ok-Jun Lee, Ki Hyeong Kim, Seung Taik |
author_facet | Lee, Joo Young Han, Hye-Suk Lim, Sung-Nam Shim, Young Kwang Choi, Yong Hyeok Lee, Ok-Jun Lee, Ki Hyeong Kim, Seung Taik |
author_sort | Lee, Joo Young |
collection | PubMed |
description | BACKGROUND: Pneumatosis intestinalis (PI), defined as the presence of gas in the bowel wall, and portal venous gas (PVG) are relatively rare radiological findings. Although several chemotherapeutic agents and anti-vascular endothelial growth factor agents are reported to be associated with PI and PVG, an association with anti-epidermal growth factor receptor (EGFR) agents has not been described previously. CASE PRESENTATION: The present report describes a case of PI and PVG secondary to treatment with an EGFR tyrosine kinase inhibitor. A 66-year-old woman who had been diagnosed with metastatic lung adenocarcinoma presented with nausea, vomiting and abdominal distension after commencing gefitinib. A computed tomography (CT) scan of the abdomen revealed PI extending from the ascending colon to the rectum, hepatic PVG, and infarction of the liver. Gefitinib therapy was discontinued immediately and the patient was managed conservatively. A follow-up CT scan 2 weeks later revealed that the PI and hepatic PVG had completely resolved. CONCLUSION: This is the first report of PI and PVG caused by EGFR tyrosine kinase inhibitor. Although these complications are extremely rare, clinicians should be aware of the risk of PI and PVG in patients undergoing targeted molecular therapy. |
format | Online Article Text |
id | pubmed-3314573 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-33145732012-03-29 Pneumatosis intestinalis and portal venous gas secondary to Gefitinib therapy for lung adenocarcinoma Lee, Joo Young Han, Hye-Suk Lim, Sung-Nam Shim, Young Kwang Choi, Yong Hyeok Lee, Ok-Jun Lee, Ki Hyeong Kim, Seung Taik BMC Cancer Case Report BACKGROUND: Pneumatosis intestinalis (PI), defined as the presence of gas in the bowel wall, and portal venous gas (PVG) are relatively rare radiological findings. Although several chemotherapeutic agents and anti-vascular endothelial growth factor agents are reported to be associated with PI and PVG, an association with anti-epidermal growth factor receptor (EGFR) agents has not been described previously. CASE PRESENTATION: The present report describes a case of PI and PVG secondary to treatment with an EGFR tyrosine kinase inhibitor. A 66-year-old woman who had been diagnosed with metastatic lung adenocarcinoma presented with nausea, vomiting and abdominal distension after commencing gefitinib. A computed tomography (CT) scan of the abdomen revealed PI extending from the ascending colon to the rectum, hepatic PVG, and infarction of the liver. Gefitinib therapy was discontinued immediately and the patient was managed conservatively. A follow-up CT scan 2 weeks later revealed that the PI and hepatic PVG had completely resolved. CONCLUSION: This is the first report of PI and PVG caused by EGFR tyrosine kinase inhibitor. Although these complications are extremely rare, clinicians should be aware of the risk of PI and PVG in patients undergoing targeted molecular therapy. BioMed Central 2012-03-10 /pmc/articles/PMC3314573/ /pubmed/22405425 http://dx.doi.org/10.1186/1471-2407-12-87 Text en Copyright ©2012 Lee et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Lee, Joo Young Han, Hye-Suk Lim, Sung-Nam Shim, Young Kwang Choi, Yong Hyeok Lee, Ok-Jun Lee, Ki Hyeong Kim, Seung Taik Pneumatosis intestinalis and portal venous gas secondary to Gefitinib therapy for lung adenocarcinoma |
title | Pneumatosis intestinalis and portal venous gas secondary to Gefitinib therapy for lung adenocarcinoma |
title_full | Pneumatosis intestinalis and portal venous gas secondary to Gefitinib therapy for lung adenocarcinoma |
title_fullStr | Pneumatosis intestinalis and portal venous gas secondary to Gefitinib therapy for lung adenocarcinoma |
title_full_unstemmed | Pneumatosis intestinalis and portal venous gas secondary to Gefitinib therapy for lung adenocarcinoma |
title_short | Pneumatosis intestinalis and portal venous gas secondary to Gefitinib therapy for lung adenocarcinoma |
title_sort | pneumatosis intestinalis and portal venous gas secondary to gefitinib therapy for lung adenocarcinoma |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3314573/ https://www.ncbi.nlm.nih.gov/pubmed/22405425 http://dx.doi.org/10.1186/1471-2407-12-87 |
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