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A childhood-onset intestinal toxemia botulism during chemotherapy for relapsed acute leukemia
BACKGROUND: Botulism is a potentially fatal infection characterized by progressive muscle weakness, bulbar paralysis, constipation and other autonomic dysfunctions. A recent report suggested that cancer chemotherapy might increase the risk for the intestinal toxemia botulism in both adults and child...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5604400/ https://www.ncbi.nlm.nih.gov/pubmed/28923072 http://dx.doi.org/10.1186/s12941-017-0240-y |
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author | Ohyama, Noriko Torio, Michiko Nakashima, Kentaro Koga, Yuuki Kanno, Shunsuke Nishio, Hisanori Nishiyama, Kei Sasazuki, Momoko Kato, Haru Asakura, Hiroshi Akamine, Satoshi Sanefuji, Masafumi Ishizaki, Yoshito Sakai, Yasunari Ohga, Shouichi |
author_facet | Ohyama, Noriko Torio, Michiko Nakashima, Kentaro Koga, Yuuki Kanno, Shunsuke Nishio, Hisanori Nishiyama, Kei Sasazuki, Momoko Kato, Haru Asakura, Hiroshi Akamine, Satoshi Sanefuji, Masafumi Ishizaki, Yoshito Sakai, Yasunari Ohga, Shouichi |
author_sort | Ohyama, Noriko |
collection | PubMed |
description | BACKGROUND: Botulism is a potentially fatal infection characterized by progressive muscle weakness, bulbar paralysis, constipation and other autonomic dysfunctions. A recent report suggested that cancer chemotherapy might increase the risk for the intestinal toxemia botulism in both adults and children. CASE PRESENTATION: We report a 5-year-old boy, who developed general muscle weakness, constipation, ptosis and mydriasis during the third induction therapy for relapsed acute myeloid leukemia. He had recent histories of multiple antibiotic therapy for bacteremia and intake of well water at home. Repeated bacterial cultures identified Clostridium botulinum producing botulinum neurotoxin A. Botulinum toxin A was isolated from his stools at 17, 21, and 23 days after the onset. Symptoms were self-limiting, and were fully recovered without anti-botulinum toxin globulin therapy. CONCLUSION: This is the second report of a pediatric case with cancer chemotherapy-associated intestinal toxemia botulism. Our case provides further evidence that the immunocompromised status due to anti-cancer treatments increases the risk for the development of botulism at all ages in childhood. |
format | Online Article Text |
id | pubmed-5604400 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-56044002017-09-21 A childhood-onset intestinal toxemia botulism during chemotherapy for relapsed acute leukemia Ohyama, Noriko Torio, Michiko Nakashima, Kentaro Koga, Yuuki Kanno, Shunsuke Nishio, Hisanori Nishiyama, Kei Sasazuki, Momoko Kato, Haru Asakura, Hiroshi Akamine, Satoshi Sanefuji, Masafumi Ishizaki, Yoshito Sakai, Yasunari Ohga, Shouichi Ann Clin Microbiol Antimicrob Case Report BACKGROUND: Botulism is a potentially fatal infection characterized by progressive muscle weakness, bulbar paralysis, constipation and other autonomic dysfunctions. A recent report suggested that cancer chemotherapy might increase the risk for the intestinal toxemia botulism in both adults and children. CASE PRESENTATION: We report a 5-year-old boy, who developed general muscle weakness, constipation, ptosis and mydriasis during the third induction therapy for relapsed acute myeloid leukemia. He had recent histories of multiple antibiotic therapy for bacteremia and intake of well water at home. Repeated bacterial cultures identified Clostridium botulinum producing botulinum neurotoxin A. Botulinum toxin A was isolated from his stools at 17, 21, and 23 days after the onset. Symptoms were self-limiting, and were fully recovered without anti-botulinum toxin globulin therapy. CONCLUSION: This is the second report of a pediatric case with cancer chemotherapy-associated intestinal toxemia botulism. Our case provides further evidence that the immunocompromised status due to anti-cancer treatments increases the risk for the development of botulism at all ages in childhood. BioMed Central 2017-09-18 /pmc/articles/PMC5604400/ /pubmed/28923072 http://dx.doi.org/10.1186/s12941-017-0240-y Text en © The Author(s) 2017 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 Ohyama, Noriko Torio, Michiko Nakashima, Kentaro Koga, Yuuki Kanno, Shunsuke Nishio, Hisanori Nishiyama, Kei Sasazuki, Momoko Kato, Haru Asakura, Hiroshi Akamine, Satoshi Sanefuji, Masafumi Ishizaki, Yoshito Sakai, Yasunari Ohga, Shouichi A childhood-onset intestinal toxemia botulism during chemotherapy for relapsed acute leukemia |
title | A childhood-onset intestinal toxemia botulism during chemotherapy for relapsed acute leukemia |
title_full | A childhood-onset intestinal toxemia botulism during chemotherapy for relapsed acute leukemia |
title_fullStr | A childhood-onset intestinal toxemia botulism during chemotherapy for relapsed acute leukemia |
title_full_unstemmed | A childhood-onset intestinal toxemia botulism during chemotherapy for relapsed acute leukemia |
title_short | A childhood-onset intestinal toxemia botulism during chemotherapy for relapsed acute leukemia |
title_sort | childhood-onset intestinal toxemia botulism during chemotherapy for relapsed acute leukemia |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5604400/ https://www.ncbi.nlm.nih.gov/pubmed/28923072 http://dx.doi.org/10.1186/s12941-017-0240-y |
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