Publications by authors named "Kazunori Tobino"

Background: Sensitization to mucus plugs, and bacterial colonization may coexist and relate to a refractory phenotype during follow-up in asthma with bronchiectasis and allergic bronchopulmonary aspergillosis (ABPA).

Objective: This study aimed to clarify the features of -sensitized refractory asthma with bronchiectasis and determine the refractory phenotype in this population and ABPA.

Methods: This study included cases of the oldest available -specific IgE data and chest computed tomography images from a nationwide survey of refractory asthma with bronchiectasis.

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A 78-year-old male who was undergoing treatment for diabetes was referred to our department after a chest X-ray revealed an abnormal shadow in the left upper lung field. A chest contrast-enhanced CT showed a tumor in the left upper lobe and a cystic lesion in the left lower lobe. Two aberrant arteries branching from the aorta were identified near the cyst.

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  • Penile Mondor's disease (PMD) is a rare and usually benign condition caused by thrombophlebitis of the superficial dorsal vein of the penis, but in this case, it was a sign of lung adenocarcinoma.
  • A 46-year-old Japanese man initially presented with PMD, which led to the diagnosis of advanced stage IVA lung cancer, complicated by deep vein thrombosis and nonbacterial thrombotic endocarditis.
  • This case emphasizes the need for doctors to consider potential underlying cancers in patients with unusual clotting issues, as well as the varied ways cancer can present itself.
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Bilateral diaphragmatic nerve paralysis due to cervical spondylosis is an extremely rare condition with only one previously reported case. We present a 64-year-old Japanese male with a history of left diaphragmatic nerve paralysis who developed sudden nocturnal dyspnea. Physical examination revealed orthopnea and type 2 respiratory failure.

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Background: We conducted a prospective observational study to elucidate the long-term prognosis and management of chronic obstructive pulmonary disease (COPD) in clinical practice in Japan in the mid-2010s.

Methods: This prospective cohort study included 29 facilities. Data from 427 patients clinically diagnosed with COPD, enrolled between September 2013 and April 2016, were analyzed.

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  • Lymphangioleiomyomatosis (LAM) is a rare lung disease mainly found in women of childbearing age but can progress in postmenopausal women, as shown in a case involving a 70-year-old patient with a long history of the disease.
  • Despite stable lung health, the patient developed abdominal lesions years after her initial diagnosis, coinciding with her breast cancer treatment using aromatase inhibitors, suggesting a link between treatments and LAM progression.
  • Sirolimus, a medication administered to the patient, effectively reduced the size of the abdominal nodules and alleviated symptoms, highlighting the need for ongoing monitoring of LAM patients beyond menopause and more investigations into treatment options and disease mechanisms.
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Trousseau's syndrome is a cancer-associated thromboembolism that significantly impacts patients' prognosis and quality of life (QOL). This study aimed to investigate the frequency, characteristics, and prognosis of Trousseau's syndrome in lung cancer patients at a Japanese community hospital and examine the effects of therapeutic agents on this condition. We retrospectively reviewed the electronic medical records of lung cancer patients diagnosed with thrombotic complications at the time of diagnosis in our department between August 2013 and April 2019.

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  • Mugwort steaming is a traditional health practice that may have benefits but poses unexamined risks to lung health.* -
  • A 48-year-old Japanese woman experienced respiratory problems related to mugwort steaming, initially diagnosed as hypersensitivity pneumonitis, but later confirmed as acute lung injury (ALI) through lung biopsy.* -
  • The case is the first documented instance of ALI linked to mugwort steaming, underscoring the need for caution with traditional practices and more research on their safety risks.*
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Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare autoimmune disorder characterized by necrotizing vasculitis, asthma, and eosinophilia. We report a case of EGPA that developed during benralizumab treatment for severe asthma and provide a literature review. A 79-year-old Japanese male with severe asthma presented with generalized purpura 4 months after initiating benralizumab treatment.

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Cryptococcosis, primarily an opportunistic infection, often occurs in immunocompromised patients but can also affect immunocompetent individuals. Cryptococcosis typically manifests in the lungs, but pleurisy is rare, particularly in immunocompetent patients. This report details a case of cryptococcal pleuritis in a 74-year-old immunocompetent male with a history of heart failure, presenting initially with pleural effusion.

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Article Synopsis
  • - Immunoglobulin A vasculitis (IgAV), or Henoch-Schönlein purpura, is a condition that leads to inflammation and bleeding in small blood vessels across various body parts, including skin and kidneys.
  • - The exact cause of IgAV is still unclear, though infections and chemicals are known triggers; this case study details an 86-year-old male who developed IgAV after receiving anti-tuberculosis treatment.
  • - This case emphasizes the need for awareness among healthcare providers that anti-tuberculous drugs may contribute to the onset of IgAV, despite scarce documentation of such occurrences.
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Immune checkpoint inhibitors (ICIs) are used to treat a variety of tumors. Despite their broad beneficial effects, these inhibitors can cause immune-related adverse events (irAEs) and even death. Hemophagocytic lymphohistiocytosis (HLH) and meningitis, although infrequent, can be aggressive and life-threatening due to excessive immune activation.

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Pulmonary amyloidosis is characterized by extracellular deposition of fibrous protein called amyloid in the lungs and has three subtypes: nodular, diffuse, and tracheobronchial amyloidosis. Pulmonary nodular amyloidosis can mimic other lung diseases including infectious diseases, metastatic lung tumors, sarcoidosis, and pulmonary hyalinizing granuloma. A biopsy of the lesion is essential for a definitive diagnosis.

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Background: Bronchial thermoplasty (BT) improves clinical outcomes and quality of life for patients with severe asthma and has shown sustained reductions in airway narrowing and air trapping in previous CT studies. However, there is a lack of a comprehensive analysis, including CT evaluation, of clinical outcomes in Japanese patients who have undergone BT for severe asthma. This study aimed to evaluate the impact of BT in Japanese asthma patients, with a focus on the CT metric "WA at Pi10" to assess airway disease.

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Background: A previous longitudinal study of chronic obstructive pulmonary disease (COPD) Assessment Test (CAT) score changes suggested patients fall into 3 patterns: stable, improving, and worsening. This study assessed the evolution of CAT scores over time and its relationship to exacerbations.

Methods: In total, 84 participants used a telemedicine platform to complete CAT weekly for 52 weeks.

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Background: Obstructive sleep apnea (OSA) occurs more commonly in asthma patients than in the general population because these conditions share some comorbidities. In Japan, the prevalence of OSA in the general population is reported to be approximately 20%; however, few reports have described the prevalence of OSA in asthma patients. Furthermore, the characteristics of Japanese patients with OSA and asthma are not clear.

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  • Biomarker testing for driver mutations in non-small cell lung cancer (NSCLC) is crucial for treatment selection, yet current practices in Japan reveal limitations.
  • The REVEAL cohort study involved data collection from 29 institutions, examining 1479 patients diagnosed with advanced or recurrent NSCLC to assess biomarker testing and treatment issues.
  • The study found that while 86.1% of patients had confirmed biomarker status, there were varying positivity rates among different gene tests, indicating challenges in effective treatment decisions based on biomarker testing.
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Objective: Few prospective cohort studies with relatively large numbers of patients with non-idiopathic pulmonary fibrosis (non-IPF) of idiopathic interstitial pneumonia (IIP) have been described. We aimed to assess disease progression and cause of death for patients with non-IPF IIPs or IPF under real-life conditions.

Methods: Data were analysed for a prospective multi-institutional cohort of 528 IIP patients enrolled in Japan between September 2013 and April 2016.

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Spontaneous pneumothorax occurs predominantly in young males and older adults, often as a secondary condition, and can be refractory and fatal. This study aimed to investigate the mortality and prognostic factors for pneumothorax in older patients. We retrospectively cohort studied patients with pneumothorax aged ≥65 years who visited our department from October 2012 to January 2019.

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Background And Objective: The relative effectiveness of initial non-invasive respiratory strategies for acute respiratory failure using continuous positive airway pressure (CPAP) or high-flow nasal cannula (HFNC) is unclear.

Methods: We conducted a multicenter, open-label, parallel-group randomized controlled trial to compare the efficacy of CPAP and HFNC on reducing the risk of meeting the prespecified criteria for intubation and improving clinical outcomes of acute hypoxemic respiratory failure. The primary endpoint was the time taken to meet the prespecified criteria for intubation within 28 days.

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  • Dacomitinib shows better outcomes than gefitinib for NSCLC patients with EGFR mutations but often causes skin toxicities that can lead to treatment stopping.
  • A study involving 41 Japanese patients tested a strategy to prevent these skin issues while they were treated with dacomitinib, focusing on managing Grade ≥2 skin toxicities in the first 8 weeks.
  • While the skin toxicity prevention approach was not particularly effective, patients were mostly compliant with their medication, highlighting the need for better patient education to help with continuity in treatment.
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Background: Skeletal muscle atrophy, a common complication of idiopathic pulmonary fibrosis (IPF), and its presence upon diagnosis can indicate a poor prognosis. Patients with IPF frequently experience acute exacerbations (AE), which is associated with a high mortality rate. However, the association between skeletal muscle atrophy and short-term mortality remains unknown.

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Background: Telemedicine may help the detection of symptom worsening in patients with chronic obstructive pulmonary disease (COPD), potentially resulting in improved outcomes. This study aimed to determine the feasibility and acceptability of telemedicine among patients with COPD and physicians and facility staff in Japan.

Methods: This was a 52-week multicenter, prospective, single-arm, feasibility and acceptability cohort study of Japanese patients ≥40 years of age with COPD or asthma-COPD overlap.

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The diagnostic criteria of aspiration pneumonia have not been established, and it remains an underdiagnosed entity. Diagnosis and cause investigation is essential in improving the management of aspiration pneumonia. The Japanese Respiratory Society Guidelines for the Management of Pneumonia in Adults (JRS Guidelines) show a list of risk factors for aspiration pneumonia.

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