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Lung parenchymal involvement of primary bone marrow follicular lymphoma: a rare case study
A 76‐year‐old man presented with shortness of breath. Computed tomography revealed ground‐glass opacity and interlobular thickening in the right lower lobe. Blood examination showed elevated levels of white blood cell count and lymphocytes. Bone marrow aspiration revealed low‐grade follicular lympho...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5812740/ https://www.ncbi.nlm.nih.gov/pubmed/29456863 http://dx.doi.org/10.1002/rcr2.302 |
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author | Minemura, Hiroyuki Hojo, Hiroshi Saito, Miwako Nikaido, Takefumi Suzuki, Tomoko Niitsuma, Katsunao |
author_facet | Minemura, Hiroyuki Hojo, Hiroshi Saito, Miwako Nikaido, Takefumi Suzuki, Tomoko Niitsuma, Katsunao |
author_sort | Minemura, Hiroyuki |
collection | PubMed |
description | A 76‐year‐old man presented with shortness of breath. Computed tomography revealed ground‐glass opacity and interlobular thickening in the right lower lobe. Blood examination showed elevated levels of white blood cell count and lymphocytes. Bone marrow aspiration revealed low‐grade follicular lymphoma. Histopathological examination of the surgical lung biopsy from the right lower lobe demonstrated usual interstitial pneumonia and scattered aggregation of lymphocytes with poorly formed non‐necrotizing granuloma. An 18F‐fluorodeoxyglucose positron emission tomography‐computed tomography (18F‐FDG PET‐CT) did not show intense uptake in areas other than the right lower lobe. We concluded that the granuloma in the lung was presumed to be a sarcoid reaction associated with bone marrow follicular lymphoma, and the intense 18F‐FDG uptake in the right lower lobe might have been due to a sarcoid reaction. Immunohistochemistry or other genetic examinations are important even if 18F‐FDG uptake on PET‐CT seems to be a false‐positive because of the possibility of a sarcoid reaction. |
format | Online Article Text |
id | pubmed-5812740 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley & Sons, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-58127402018-02-16 Lung parenchymal involvement of primary bone marrow follicular lymphoma: a rare case study Minemura, Hiroyuki Hojo, Hiroshi Saito, Miwako Nikaido, Takefumi Suzuki, Tomoko Niitsuma, Katsunao Respirol Case Rep Case Reports A 76‐year‐old man presented with shortness of breath. Computed tomography revealed ground‐glass opacity and interlobular thickening in the right lower lobe. Blood examination showed elevated levels of white blood cell count and lymphocytes. Bone marrow aspiration revealed low‐grade follicular lymphoma. Histopathological examination of the surgical lung biopsy from the right lower lobe demonstrated usual interstitial pneumonia and scattered aggregation of lymphocytes with poorly formed non‐necrotizing granuloma. An 18F‐fluorodeoxyglucose positron emission tomography‐computed tomography (18F‐FDG PET‐CT) did not show intense uptake in areas other than the right lower lobe. We concluded that the granuloma in the lung was presumed to be a sarcoid reaction associated with bone marrow follicular lymphoma, and the intense 18F‐FDG uptake in the right lower lobe might have been due to a sarcoid reaction. Immunohistochemistry or other genetic examinations are important even if 18F‐FDG uptake on PET‐CT seems to be a false‐positive because of the possibility of a sarcoid reaction. John Wiley & Sons, Ltd 2018-02-14 /pmc/articles/PMC5812740/ /pubmed/29456863 http://dx.doi.org/10.1002/rcr2.302 Text en © 2018 The Authors. Respirology Case Reports published by John Wiley & Sons Australia, Ltd on behalf of The Asian Pacific Society of Respirology This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Case Reports Minemura, Hiroyuki Hojo, Hiroshi Saito, Miwako Nikaido, Takefumi Suzuki, Tomoko Niitsuma, Katsunao Lung parenchymal involvement of primary bone marrow follicular lymphoma: a rare case study |
title | Lung parenchymal involvement of primary bone marrow follicular lymphoma: a rare case study |
title_full | Lung parenchymal involvement of primary bone marrow follicular lymphoma: a rare case study |
title_fullStr | Lung parenchymal involvement of primary bone marrow follicular lymphoma: a rare case study |
title_full_unstemmed | Lung parenchymal involvement of primary bone marrow follicular lymphoma: a rare case study |
title_short | Lung parenchymal involvement of primary bone marrow follicular lymphoma: a rare case study |
title_sort | lung parenchymal involvement of primary bone marrow follicular lymphoma: a rare case study |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5812740/ https://www.ncbi.nlm.nih.gov/pubmed/29456863 http://dx.doi.org/10.1002/rcr2.302 |
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