@article{oai:nagasaki-u.repo.nii.ac.jp:00027820,
 author = {Moriyama, Sakiko and Kido, Takashi and Sakamoto, Noriho and Fuchigami, Mai and Tokito, Takatomo and Okuno, Daisuke and Miyamura, Takuto and Nakashima, Shota and Hara, Atsuko and Ishimoto, Hiroshi and Imaizumi, Yoshitaka and Tsuruda, Kazuto and Yanagihara, Katsunori and Fukuoka, Junya and Mukae, Hiroshi},
 issue = {1},
 journal = {Internal Medicine},
 month = {Jan},
 note = {Pulmonary nodular lymphoid hyperplasia (PNLH) is a very rare disease, and it is difficult to diagnose PNLH and distinguish it from mucosa-associated lymphoid tissue (MALT) lymphoma. In addition, information on bronchoalveolar lavage fluid (BALF) analyses is lacking. We herein report a 36-year-old Japanese woman diagnosed with PLNH by a surgical biopsy and analysis of BALF. The BALF showed an increase in B-cell marker-positive lymphocytes, normal patterns of B-cell clonality, mucosa-associated lymphoid tissue 1 gene, and immunoglobulin heavy chain at 14q32 translocations. We also reviewed Japanese cases of PNLH
described in Japanese or English to explore the characteristics of such cases., Internal Medicine, 62(1), pp.95-102; 2023},
 pages = {95--102},
 title = {Pulmonary Nodular Lymphoid Hyperplasia Evaluated with Bronchoalveolar Lavage Fluid Findings: A Case Report and Review of the Literature on Japanese Patients},
 volume = {62},
 year = {2023}
}