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Achromobacter Infection Is Rare in Japanese Patients with Pulmonary B-cell Lymphoma

OBJECTIVE: Achromobacter xylosoxidans (A. xylosoxidans) has been recently reported to have an association with the development of pulmonary mucosa-associated lymphoid tissue (MALT) lymphoma in patients from European countries. However, the prevalence rates for A. xylosoxidans may vary significantly...

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Autores principales: Aoyama, Satsuki, Masaki, Ayako, Sakamoto, Yuma, Takino, Hisashi, Murase, Takayuki, Ohshima, Koichi, Yoshino, Tadashi, Kato, Seiichi, Inagaki, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Internal Medicine 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5891515/
https://www.ncbi.nlm.nih.gov/pubmed/29151525
http://dx.doi.org/10.2169/internalmedicine.9430-17
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author Aoyama, Satsuki
Masaki, Ayako
Sakamoto, Yuma
Takino, Hisashi
Murase, Takayuki
Ohshima, Koichi
Yoshino, Tadashi
Kato, Seiichi
Inagaki, Hiroshi
author_facet Aoyama, Satsuki
Masaki, Ayako
Sakamoto, Yuma
Takino, Hisashi
Murase, Takayuki
Ohshima, Koichi
Yoshino, Tadashi
Kato, Seiichi
Inagaki, Hiroshi
author_sort Aoyama, Satsuki
collection PubMed
description OBJECTIVE: Achromobacter xylosoxidans (A. xylosoxidans) has been recently reported to have an association with the development of pulmonary mucosa-associated lymphoid tissue (MALT) lymphoma in patients from European countries. However, the prevalence rates for A. xylosoxidans may vary significantly from country to country. To assess this association, the prevalence of A. xylosoxidans was analyzed in Japanese patients with pulmonary B-cell lymphoma. METHODS: DNA samples were obtained from formalin-fixed, paraffin-embedded sections of pulmonary MALT lymphomas (n=52), diffuse large B-cell lymphomas (DLBCLs, n=18), and benign pulmonary lesions (n=19). All samples were histopathologically reviewed by experienced hematopathologists, and the clonality of all MALT lymphoma cases was confirmed by a polymerase chain reaction (PCR)-based IGH rearrangement clonality assay. They were also tested for the API2-MALT1 fusion transcript. The presence of bacterial DNA was assessed with a nested PCR, and DNA sequencing was performed to confirm the PCR specificity. RESULTS: A. xylosoxidans DNA was detected in 1/52 cases of pulmonary MALT lymphoma, 2/18 cases of DLBCL, and 0/19 cases of benign pulmonary lesions. The prevalence of A. xylosoxidans in pulmonary lymphoma was not significantly higher than in benign lesions. CONCLUSION: The present study shows that A. xylosoxidans infection may not be associated with pulmonary B-cell lymphoma in a Japanese case series. Large-scale international studies are needed to clarify the role of A. xylosoxidans in pulmonary lymphoma.
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spelling pubmed-58915152018-04-12 Achromobacter Infection Is Rare in Japanese Patients with Pulmonary B-cell Lymphoma Aoyama, Satsuki Masaki, Ayako Sakamoto, Yuma Takino, Hisashi Murase, Takayuki Ohshima, Koichi Yoshino, Tadashi Kato, Seiichi Inagaki, Hiroshi Intern Med Original Article OBJECTIVE: Achromobacter xylosoxidans (A. xylosoxidans) has been recently reported to have an association with the development of pulmonary mucosa-associated lymphoid tissue (MALT) lymphoma in patients from European countries. However, the prevalence rates for A. xylosoxidans may vary significantly from country to country. To assess this association, the prevalence of A. xylosoxidans was analyzed in Japanese patients with pulmonary B-cell lymphoma. METHODS: DNA samples were obtained from formalin-fixed, paraffin-embedded sections of pulmonary MALT lymphomas (n=52), diffuse large B-cell lymphomas (DLBCLs, n=18), and benign pulmonary lesions (n=19). All samples were histopathologically reviewed by experienced hematopathologists, and the clonality of all MALT lymphoma cases was confirmed by a polymerase chain reaction (PCR)-based IGH rearrangement clonality assay. They were also tested for the API2-MALT1 fusion transcript. The presence of bacterial DNA was assessed with a nested PCR, and DNA sequencing was performed to confirm the PCR specificity. RESULTS: A. xylosoxidans DNA was detected in 1/52 cases of pulmonary MALT lymphoma, 2/18 cases of DLBCL, and 0/19 cases of benign pulmonary lesions. The prevalence of A. xylosoxidans in pulmonary lymphoma was not significantly higher than in benign lesions. CONCLUSION: The present study shows that A. xylosoxidans infection may not be associated with pulmonary B-cell lymphoma in a Japanese case series. Large-scale international studies are needed to clarify the role of A. xylosoxidans in pulmonary lymphoma. The Japanese Society of Internal Medicine 2017-11-20 2018-03-15 /pmc/articles/PMC5891515/ /pubmed/29151525 http://dx.doi.org/10.2169/internalmedicine.9430-17 Text en Copyright © 2018 by The Japanese Society of Internal Medicine https://creativecommons.org/licenses/by-nc-nd/4.0/ The Internal Medicine is an Open Access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Aoyama, Satsuki
Masaki, Ayako
Sakamoto, Yuma
Takino, Hisashi
Murase, Takayuki
Ohshima, Koichi
Yoshino, Tadashi
Kato, Seiichi
Inagaki, Hiroshi
Achromobacter Infection Is Rare in Japanese Patients with Pulmonary B-cell Lymphoma
title Achromobacter Infection Is Rare in Japanese Patients with Pulmonary B-cell Lymphoma
title_full Achromobacter Infection Is Rare in Japanese Patients with Pulmonary B-cell Lymphoma
title_fullStr Achromobacter Infection Is Rare in Japanese Patients with Pulmonary B-cell Lymphoma
title_full_unstemmed Achromobacter Infection Is Rare in Japanese Patients with Pulmonary B-cell Lymphoma
title_short Achromobacter Infection Is Rare in Japanese Patients with Pulmonary B-cell Lymphoma
title_sort achromobacter infection is rare in japanese patients with pulmonary b-cell lymphoma
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5891515/
https://www.ncbi.nlm.nih.gov/pubmed/29151525
http://dx.doi.org/10.2169/internalmedicine.9430-17
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