7 results match your criteria: "National Hospital Organization MinamiKyushu Hospital[Affiliation]"

Background: Reports of autoimmune diseases coexisting with autoimmune pulmonary alveolar proteinosis (autoimmune PAP; APAP) are extremely rare. APAP coexisting with autoimmune diseases may often be misdiagnosed as connective tissue disease-associated interstitial lung disease (ILD). Here, we describe a rare case of a patient with systemic sclerosis who was diagnosed with APAP after the exacerbation of lung opacities during treatment with immunosuppressive agents.

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Article Synopsis
  • Patients with early-stage lung cancer and interstitial lung disease generally have worse outcomes compared to those without the lung disease.
  • A study analyzed the long-term outcomes of 138 patients who underwent either sublobar or lobar resection for lung cancer, finding that lobar resections led to significantly better survival and recurrence-free rates.
  • The results suggest that lobar resection improves survival rates, indicating that less extensive surgical options may not be warranted for patients who can tolerate a lobectomy.
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Osimertinib has demonstrated efficacy as the first- and second-line treatment for advanced non-small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) gene mutations. However, EGFR-mutant NSCLC cells often acquire resistance to osimertinib. V-Raf murine sarcoma viral oncogene homolog B1 (BRAF) mutation (BRAF V600E) was detected in a re-biopsy (LC-SCRUM-TRY testing) of a patient with advanced lung adenocarcinoma who was resistant to osimertinib treatment.

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Article Synopsis
  • The study investigates the genetic causes of late-onset cerebellar ataxia in Japan, focusing on GAA repeat expansions in the FGF14 gene.
  • Analysis of 940 patients revealed pathogenic FGF14 GAA repeat expansions in 12 patients, with a median size of 309 repeats and an average age of onset of nearly 67 years.
  • The findings suggest that FGF14 GAA repeat analysis is crucial for diagnosing cerebellar ataxia, especially in cases with episodic symptoms or normal MRI results, enhancing the understanding of this genetic disorder.
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We report a case of a 60-year-old man who presented with symptoms of memory loss, gait disorder, and sluggish movement. We considered both Parkinson's disease and multiple system atrophy as possible diagnoses and consequently hospitalized the patient owing to the worsening symptoms and the development of consciousness disorder. During the course of the disease, dementia, loss of consciousness, and movement disorders worsened rapidly within one year after admission, and the patient eventually developed mutism.

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Novel approach to pleurodesis with 50 % glucose for air leakage after lung resection or pneumothorax.

Surg Today

May 2016

Department of Thoracic Surgery, Graduate School of Medical Sciences, Kumamoto University, 1-1-1 Honjo, Kumamoto, Japan.

Purpose: Pleurodesis is performed in patients demonstrating air leakage after lung resection and in those with pneumothorax who must avoid surgery. However, there have so far been very few reports of pleurodesis with 50 % glucose. We herein examined the feasibility and effectiveness of this novel pleurodesis technique.

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