Updated on 2025/03/27

写真a

 
Nakamura Yukihiro
 
Organization
University Hospital Assistant Professor
Title
Assistant Professor
Contact information
メールアドレス
External link

Degree

  • 学士（医学） ( 2013.3   香川大学 )

Research Areas

  • Life Science / Respiratory medicine

Papers

  • Mediastinal undifferentiated pleomorphic sarcoma with pleural effusion cytopathologically misdiagnosed as epithelial malignant pleural mesothelioma: An autopsy case report. International journal

    Kinnosuke Matsumoto, Yukihiro Nakamura, Yuji Inagaki, Yoshihiko Taniguchi, Akihiro Tamiya, Yoshinobu Matsuda, Takahiko Kasai, Shinji Atagi

    Thoracic cancer   12 ( 7 )   1137 - 1140   2021.4

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    Language：English   Publishing type：Research paper (scientific journal)  

    Undifferentiated pleomorphic sarcoma (UPS) is a new disease in the World Health Organization's classification of tumors of soft tissue and bone published in 2013. Primary mediastinal UPS is rare, especially with pleural effusion. Herein, we describe the pathological findings of pleural effusion followed by mediastinal UPS, which was initially misdiagnosed as epithelial malignant pleural mesothelioma (MPM). The cytopathological findings of the pleural effusion cell block often contribute to the diagnosis of various malignant tumors. However, these findings may lead to misdiagnosis of highly invasive mediastinal tumors such as UPS. A biopsy for primary mediastinal lesions should be performed because MPM rarely mimics mediastinal tumors with pleural effusion.

    DOI： 10.1111/1759-7714.13898

    PubMed

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  • Drug-related pneumonitis with radiographic hypersensitivity pneumonitis pattern: Three case series. International journal

    Yukihiro Nakamura, Takayuki Takimoto, Takehiko Kobayashi, Kazunobu Tachibana, Takahiko Kasai, Masanobu Akira, Toru Arai, Yoshikazu Inoue

    Respiratory medicine case reports   34   101498 - 101498   2021

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    Language：English  

    Novel therapies have recently emerged for various diseases, and the management of drug-related pneumonitis (DRP) has become increasingly important. In particular, the hypersensitivity pneumonitis (HP) pattern of DRP has been increasingly recognized due to development of new therapeutic strategies, such as immunotherapy. However, literature describing detailed clinical cases is still lacking. Herein, we report three cases of DRP with typical HP radiographic pattern. These patients were treated with different drugs, namely nano albumin-bound (nab)-paclitaxel, everolimus, or nivolumab, but had common clinical features, including a good prognosis.

    DOI： 10.1016/j.rmcr.2021.101498

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  • Meaningful Symptoms of Immune Checkpoint Inhibitor Therapy-Related Gastrointestinal Adverse Events in Patients With Inflammatory Bowel Disease. International journal

    Yuji Inagaki, Kouji Azuma, Yukihiro Nakamura, Shunichi Kouno, Yoshinobu Matsuda, Shinji Atagi

    Journal of clinical oncology : official journal of the American Society of Clinical Oncology   38 ( 15 )   1748 - 1749   2020.5

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  • Progressive Aortic Calcification as a Complication of Dermatomyositis.

    Seigo Miyoshi, Takuya Matsumoto, Teruki Kidani, Eiji Sugimoto, Yukihiro Nakamura, Tetsuya Yamamoto, Takahide Kato, Shoicihiro Yamamoto, Chizuru Hamada, Naohiko Hamaguchi, Yasuhito Hamaguchi, Osamu Yamaguchi

    Circulation journal : official journal of the Japanese Circulation Society   83 ( 9 )   1972 - 1972   2019.8

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  • Pulmonary Hemorrhaging as a Fatal Complication of IgA Vasculitis.

    Seigo Miyoshi, Tomoaki Nagao, Masayoshi Kukida, Ken-Ichi Miyoshi, Chika Namba, Sohei Kitazawa, Yukihiro Nakamura, Naohiko Hamaguchi, Jitsuo Higaki

    Internal medicine (Tokyo, Japan)   57 ( 21 )   3141 - 3147   2018.11

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    Language：English   Publishing type：Research paper (scientific journal)  

    A 64-year-old man was admitted to our hospital for purpuric rash, joint pain, and a fever. He had earlier undergone a follow-up examination for interstitial lung disease. At the current visit, the diagnosis was immunoglobulin A (IgA) vasculitis, based on skin and renal biopsy findings. He developed sudden breathlessness and hemoptysis. Chest computed tomography revealed ground glass opacity in the right lower lung fields, suggesting pulmonary hemorrhaging associated with IgA vasculitis. Despite steroid and cyclophosphamide therapy, and plasma exchange, he died 52 days after admission. Early aggressive therapies may be recommended for old patients with IgA vasculitis who have an additional comorbidities.

    DOI： 10.2169/internalmedicine.0817-18

    PubMed

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