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Pulmonary Nodular Lymphoid Hyperplasia in a 33-Year-Old Woman

Pulmonary nodular lymphoid hyperplasia is a reactive lymphoproliferative disease. It is very rare, which means that many aspects of the disease are unknown or have not been proven. Pulmonary nodular lymphoid hyperplasia can be symptomatic or asymptomatic, progressive or not, and solitary or multiple...

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Autores principales: Park, Ji Ye, Park, Seong Yong, Haam, Seokjin, Jung, Joonho, Koh, Young Wha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Thoracic and Cardiovascular Surgery 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5894578/
https://www.ncbi.nlm.nih.gov/pubmed/29662812
http://dx.doi.org/10.5090/kjtcs.2018.51.2.133
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author Park, Ji Ye
Park, Seong Yong
Haam, Seokjin
Jung, Joonho
Koh, Young Wha
author_facet Park, Ji Ye
Park, Seong Yong
Haam, Seokjin
Jung, Joonho
Koh, Young Wha
author_sort Park, Ji Ye
collection PubMed
description Pulmonary nodular lymphoid hyperplasia is a reactive lymphoproliferative disease. It is very rare, which means that many aspects of the disease are unknown or have not been proven. Pulmonary nodular lymphoid hyperplasia can be symptomatic or asymptomatic, progressive or not, and solitary or multiple, and a surgical approach is the current treatment of choice. We present a case of pulmonary nodular lymphoid hyperplasia that was visualized as multiple ground glass opacities on a computed tomography (CT) scan, and observed for 1 year because the patient was pregnant. Over this period, the number and extent of the opacities progressed, but no symptoms were reported. A surgical biopsy was done and some remaining lesions regressed on follow-up CT scans, while others progressed, without any appearance of symptoms.
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spelling pubmed-58945782018-04-16 Pulmonary Nodular Lymphoid Hyperplasia in a 33-Year-Old Woman Park, Ji Ye Park, Seong Yong Haam, Seokjin Jung, Joonho Koh, Young Wha Korean J Thorac Cardiovasc Surg Case Report Pulmonary nodular lymphoid hyperplasia is a reactive lymphoproliferative disease. It is very rare, which means that many aspects of the disease are unknown or have not been proven. Pulmonary nodular lymphoid hyperplasia can be symptomatic or asymptomatic, progressive or not, and solitary or multiple, and a surgical approach is the current treatment of choice. We present a case of pulmonary nodular lymphoid hyperplasia that was visualized as multiple ground glass opacities on a computed tomography (CT) scan, and observed for 1 year because the patient was pregnant. Over this period, the number and extent of the opacities progressed, but no symptoms were reported. A surgical biopsy was done and some remaining lesions regressed on follow-up CT scans, while others progressed, without any appearance of symptoms. The Korean Society for Thoracic and Cardiovascular Surgery 2018-04 2018-04-05 /pmc/articles/PMC5894578/ /pubmed/29662812 http://dx.doi.org/10.5090/kjtcs.2018.51.2.133 Text en Copyright © 2018 by The Korean Society for Thoracic and Cardiovascular Surgery. All rights Reserved. This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Park, Ji Ye
Park, Seong Yong
Haam, Seokjin
Jung, Joonho
Koh, Young Wha
Pulmonary Nodular Lymphoid Hyperplasia in a 33-Year-Old Woman
title Pulmonary Nodular Lymphoid Hyperplasia in a 33-Year-Old Woman
title_full Pulmonary Nodular Lymphoid Hyperplasia in a 33-Year-Old Woman
title_fullStr Pulmonary Nodular Lymphoid Hyperplasia in a 33-Year-Old Woman
title_full_unstemmed Pulmonary Nodular Lymphoid Hyperplasia in a 33-Year-Old Woman
title_short Pulmonary Nodular Lymphoid Hyperplasia in a 33-Year-Old Woman
title_sort pulmonary nodular lymphoid hyperplasia in a 33-year-old woman
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5894578/
https://www.ncbi.nlm.nih.gov/pubmed/29662812
http://dx.doi.org/10.5090/kjtcs.2018.51.2.133
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