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Gefitinib successfully administered in a lung cancer patient with leptomeningeal carcinomatosis after erlotinib-induced pneumatosis intestinalis

BACKGROUND: Pneumatosis intestinalis (PI) is a rare complication of chemotherapy, characterized by multiple gas accumulations within the bowel wall. CASE PRESENTATION: A 71-year-old woman with epidermal growth factor receptor (EGFR) mutation-positive lung adenocarcinoma was admitted to our hospital...

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Autores principales: Uruga, Hironori, Moriguchi, Shuhei, Takahashi, Yui, Ogawa, Kazumasa, Murase, Kyoko, Mochizuki, Sayaka, Hanada, Shigeo, Takaya, Hisashi, Miyamoto, Atsushi, Morokawa, Nasa, Kishi, Kazuma
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6097412/
https://www.ncbi.nlm.nih.gov/pubmed/30115025
http://dx.doi.org/10.1186/s12885-018-4743-5
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author Uruga, Hironori
Moriguchi, Shuhei
Takahashi, Yui
Ogawa, Kazumasa
Murase, Kyoko
Mochizuki, Sayaka
Hanada, Shigeo
Takaya, Hisashi
Miyamoto, Atsushi
Morokawa, Nasa
Kishi, Kazuma
author_facet Uruga, Hironori
Moriguchi, Shuhei
Takahashi, Yui
Ogawa, Kazumasa
Murase, Kyoko
Mochizuki, Sayaka
Hanada, Shigeo
Takaya, Hisashi
Miyamoto, Atsushi
Morokawa, Nasa
Kishi, Kazuma
author_sort Uruga, Hironori
collection PubMed
description BACKGROUND: Pneumatosis intestinalis (PI) is a rare complication of chemotherapy, characterized by multiple gas accumulations within the bowel wall. CASE PRESENTATION: A 71-year-old woman with epidermal growth factor receptor (EGFR) mutation-positive lung adenocarcinoma was admitted to our hospital because of reduced consciousness. She was diagnosed as having leptomeningeal carcinomatosis (LM) using lumbar puncture. Because she could not swallow a tablet, erlotinib was administered via a feeding tube. Her state of consciousness gradually improved, but she experienced diarrhea several times a day. After 3 weeks of erlotinib therapy, PI occurred. Erlotinib was discontinued and PI was resolved after treatment with conservative therapies. Erlotinib was re-administrated and PI occurred again. After improvement of erlotinib-induced PI, gefitinib was administered by a feeding tube and the patient did not experience PI or diarrhea. The patient survived 8 months from the diagnosis of LM. CONCLUSION: PI is one of the side effects of erlotinib, and consecutive therapies are useful for the treatment of PI. In this patient, gefitinib was successfully administered after erlotinib-induced PI.
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spelling pubmed-60974122018-08-20 Gefitinib successfully administered in a lung cancer patient with leptomeningeal carcinomatosis after erlotinib-induced pneumatosis intestinalis Uruga, Hironori Moriguchi, Shuhei Takahashi, Yui Ogawa, Kazumasa Murase, Kyoko Mochizuki, Sayaka Hanada, Shigeo Takaya, Hisashi Miyamoto, Atsushi Morokawa, Nasa Kishi, Kazuma BMC Cancer Case Report BACKGROUND: Pneumatosis intestinalis (PI) is a rare complication of chemotherapy, characterized by multiple gas accumulations within the bowel wall. CASE PRESENTATION: A 71-year-old woman with epidermal growth factor receptor (EGFR) mutation-positive lung adenocarcinoma was admitted to our hospital because of reduced consciousness. She was diagnosed as having leptomeningeal carcinomatosis (LM) using lumbar puncture. Because she could not swallow a tablet, erlotinib was administered via a feeding tube. Her state of consciousness gradually improved, but she experienced diarrhea several times a day. After 3 weeks of erlotinib therapy, PI occurred. Erlotinib was discontinued and PI was resolved after treatment with conservative therapies. Erlotinib was re-administrated and PI occurred again. After improvement of erlotinib-induced PI, gefitinib was administered by a feeding tube and the patient did not experience PI or diarrhea. The patient survived 8 months from the diagnosis of LM. CONCLUSION: PI is one of the side effects of erlotinib, and consecutive therapies are useful for the treatment of PI. In this patient, gefitinib was successfully administered after erlotinib-induced PI. BioMed Central 2018-08-16 /pmc/articles/PMC6097412/ /pubmed/30115025 http://dx.doi.org/10.1186/s12885-018-4743-5 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Uruga, Hironori
Moriguchi, Shuhei
Takahashi, Yui
Ogawa, Kazumasa
Murase, Kyoko
Mochizuki, Sayaka
Hanada, Shigeo
Takaya, Hisashi
Miyamoto, Atsushi
Morokawa, Nasa
Kishi, Kazuma
Gefitinib successfully administered in a lung cancer patient with leptomeningeal carcinomatosis after erlotinib-induced pneumatosis intestinalis
title Gefitinib successfully administered in a lung cancer patient with leptomeningeal carcinomatosis after erlotinib-induced pneumatosis intestinalis
title_full Gefitinib successfully administered in a lung cancer patient with leptomeningeal carcinomatosis after erlotinib-induced pneumatosis intestinalis
title_fullStr Gefitinib successfully administered in a lung cancer patient with leptomeningeal carcinomatosis after erlotinib-induced pneumatosis intestinalis
title_full_unstemmed Gefitinib successfully administered in a lung cancer patient with leptomeningeal carcinomatosis after erlotinib-induced pneumatosis intestinalis
title_short Gefitinib successfully administered in a lung cancer patient with leptomeningeal carcinomatosis after erlotinib-induced pneumatosis intestinalis
title_sort gefitinib successfully administered in a lung cancer patient with leptomeningeal carcinomatosis after erlotinib-induced pneumatosis intestinalis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6097412/
https://www.ncbi.nlm.nih.gov/pubmed/30115025
http://dx.doi.org/10.1186/s12885-018-4743-5
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