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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...

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Autores principales: Minemura, Hiroyuki, Hojo, Hiroshi, Saito, Miwako, Nikaido, Takefumi, Suzuki, Tomoko, Niitsuma, Katsunao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd 2018
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.
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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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