9 results match your criteria: "The Second Department of Internal Medicine University of Occupational and Environmental Health[Affiliation]"

Background: The cause of chronic thromboembolic pulmonary hypertension (CTEPH) remains largely unknown. Recently, clonal hematopoiesis (CH) has been reported to be associated with cardiovascular and thromboembolic diseases. Here, we investigated the prevalence and clinical impact of CH in patients with CTEPH.

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We presented a detailed time course of RFCA-associated PV calcification process. Because RFCA-associated PV calcification may progress over time even with a single ablation, long-term caution should be paid in cases of especially extensive ablation and/or patients with stiff LA syndrome.

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Background: The effect of cardiac rehabilitation (CR) on patients undergoing device implantation (DI) for arrhythmias has been reported; however, the implementation status of these patients has not been clarified. This study aimed to verify the implementation status of CR for patients with heart disease who have undergone DI using real-world data.

Methods: This was an observational study using a nationwide administrative database associated with the diagnosis procedure combination (DPC) system in Japan (2014-2018).

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We reported a case of early S-ICD shock due to the carryover of previously charged energy. Depending on the interval with the preceding event, an early shock may occur for the subsequent event. Especially, in cases where non-sustained VTs occur frequently, the indication for S-ICD surgery should be considered carefully.

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Article Synopsis
  • Researchers found a new gene variant (p.Gly76Ser) linked to pulmonary artery hypertension (PAH) in 6 out of 242 Japanese patients studied.
  • This variant affects a gene involved in B cell differentiation and inflammatory responses, suggesting it may play a role in vascular inflammation.
  • Structural analysis indicates that this gene variant could lead to instability in protein structure, implicating it as a potential new cause of PAH.
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Rod-like inclusions have rarely been described in cases of monoclonal gammopathy of renal significance or multiple myeloma. The key finding in our case is the strong κ-light chain positivity of rod-like inclusions in plasma cells, which confirms their immunoglobulin nature. Therapeutic benefit of bortezomib was also observed.

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Cronkhite-Canada syndrome: report of two cases.

J Gastroenterol

May 2001

Third Department of Internal Medicine. University of Occupational and Environmental Health, Japan, School of Medicine, Kitakyushu.

Two cases of Cronkhite-Canada syndrome are reported. In the first case, a 56-year-old woman had an adenoma of the colon, arising within the Cronkhite-Canada polyps, which was removed by endoscopic polypectomy. This suggests possible neoplastic transformation of polyps in this syndrome.

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[A case of myeloperoxidase-antineutrophil cytoplasmic antibody (ANCA)-positive crescentic glomerulonephritis induced by propylthiouracil (PTU)].

Nihon Jinzo Gakkai Shi

July 1997

Second Department of Internal Medicine University of Occupational and Environmental Health, School of Medicine, Kitakyushu, Japan.

We have experienced a case of myeloperoxidase-antineutrophil cytoplasmic antibody (MPO-ANCA)-related glomerulonephritis induced by propylthiouracil (PTU). A 45-year-old female had been treated with PTU for 4 years after the diagnosis of hyperthyroidism. She was referred to out hospital because of abrupt macroscopic hematuria and moderate proteinuria after several days of upper respiratory tract infection.

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[Renovascular hypertension associated with antiphospholipid antibodies in a woman with systemic lupus erythematosus].

Nihon Jinzo Gakkai Shi

September 1996

Second Department of Internal Medicine University of Occupational and Environmental Health, School of Medicine, Kitakyushu, Japan.

Systemic lupus erythematosus (SLE) patients, especially those with antiphospholipid antibodies, have a high incidence of arterial and venous thrombotic manifestations. However, renovascular hypertension (RVH) has been rarely reported in these patients. We describe here a 49-year-old female with antiphospholipid antibodies, complicated with RVH and presenting with sudden onset of severe hypertension, headache and nausea.

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