Publications by authors named "Mitsuhiro Moda"

Background: Approximately 20% of patients with pulmonary alveolar proteinosis (PAP) present with pulmonary fibrosis on high-resolution computed tomography (HRCT). Although transbronchial lung cryobiopsy (TBLC) has recently been used to diagnose fibrotic interstitial lung disease, no studies have investigated whether TBLC is useful for the histopathological detection of pulmonary fibrosis coexisting with PAP. Therefore, the present study aimed to investigate the utility of TBLC for evaluating pulmonary fibrosis in patients with PAP.

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Article Synopsis
  • - Idiopathic inflammatory myopathies (IIM) are autoimmune diseases primarily affecting muscles and can lead to serious complications like interstitial lung disease (ILD), which significantly impacts survival and quality of life.
  • - Myositis-specific antibody (MSA) profiles help determine different clinical responses, prognoses, and racial differences in IIM-ILD; for instance, the anti-melanoma differentiation-associated gene 5 antibody is linked to rapidly progressive ILD (RP-ILD), especially in Asian populations.
  • - Early aggressive treatment with corticosteroids and immunosuppressants can improve outcomes for IIM-ILD, but patients with certain antibodies, like anti-aminoacyl-tRNA synthetase (ARS), may have a
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Article Synopsis
  • Many patients with anti-synthetase syndrome-associated interstitial lung disease (ASS-ILD) can have a mild form that doesn't require immediate treatment and is stable over time.
  • In a study of 80 patients, 33 were identified as having a less aggressive form (indolent-ASS-ILD), with 90% showing stability after 24 months of a watch-and-wait approach.
  • While most patients did not experience significant lung function decline, some showed lung fibrosis progression on imaging, particularly those with elevated levels of KL-6 and SP-D, indicating the need for monitoring despite a stable clinical course.
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The prognosis of patients with coronavirus disease 2019 (COVID-19) and pre-existing interstitial lung disease (preILD) is poor, and no effective treatment strategy has been determined. The aim of this study was to assess the effectiveness of a steroid-based treatment strategy for patients with COVID-19 and preILD. We retrospectively reviewed the medical records of 610 consecutive patients with COVID-19 treated at our institution between 1 March 2020 and 30 October 2021 and identified 7 patients with preILD, all of whom were treated with corticosteroids and remdesivir.

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A 79-year-old man was admitted with worsening cough, dyspnea, and increased ground-glass opacity on chest computed tomography (CT). He had been diagnosed with idiopathic pulmonary fibrosis given the absence of an identifiable cause of interstitial pneumonia, chest CT findings, and absence of lymphocytosis in bronchoalveolar lavage (BAL) fluid. Meticulous history taking revealed extensive exposure to inciting antigens contained in chicken fertilizer before symptom worsening.

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Background: Ulcerative colitis (UC) is a chronic GI inflammatory disorder involving various extraintestinal organs, including the lungs. Although UC-related lung diseases (UC-LDs) have been widely recognized, much remains unclear.

Research Question: What are the incidence, characteristics, clinical course, and risk factors of UC-LD?

Study Design And Methods: This study retrospectively identified and classified UC-LDs by reviewing the medical records of consecutive patients with UC.

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A 57-year-old woman was referred to our hospital for investigation of multiple tiny nodules in the lung fields bilaterally on computed tomography (CT). Video-assisted thoracoscopic lung biopsy was performed to diagnose the pulmonary lesions. Histological analysis showed nodular lesions with interstitial proliferation of uniform, round to oval cells with variable widening of the alveolar septa.

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Background: Anti-programmed death-1 (PD-1) immunotherapy can cause immune-related pneumonitis, also known as checkpoint inhibitor pneumonitis (CIP). CIP that develops early after the initiation of anti-PD-1 immunotherapy is important because it is more severe than CIP that develops later. However, only a few studies have examined the risk factors for early-onset CIP.

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A 50-year-old man was admitted with respiratory failure. Chest X-ray and computed tomography revealed massive left pleural effusion and mediastinal shift. Pleural effusion showed abnormally high amylase levels of 42,600 IU/l and a high protein level of 3.

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