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288 results on '"Sato, Mari"'

6. Practical Criterion of Flow Stability in Unsaturated Soil

Author

Sato, Mari, Pisello, Anna Laura, Editorial Board Member, Hawkes, Dean, Editorial Board Member, Bougdah, Hocine, Editorial Board Member, Rosso, Federica, Editorial Board Member, Abdalla, Hassan, Editorial Board Member, Boemi, Sofia-Natalia, Editorial Board Member, Mohareb, Nabil, Editorial Board Member, Mesbah Elkaffas, Saleh, Editorial Board Member, Bozonnet, Emmanuel, Editorial Board Member, Pignatta, Gloria, Editorial Board Member, Mahgoub, Yasser, Editorial Board Member, De Bonis, Luciano, Editorial Board Member, Kostopoulou, Stella, Editorial Board Member, Pradhan, Biswajeet, Editorial Board Member, Abdul Mannan, Md., Editorial Board Member, Alalouch, Chaham, Editorial Board Member, O. Gawad, Iman, Editorial Board Member, Nayyar, Anand, Editorial Board Member, Amer, Mourad, Series Editor, El-Askary, Hesham, editor, Erguler, Zeynal Abiddin, editor, Karakus, Murat, editor, and Chaminé, Helder I., editor

Published
2022
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13. A case of autoimmune pulmonary alveolar proteinosis during the course of treatment of rapidly progressive interstitial pneumonia associated with anti-MDA5 antibody-positive dermatomyositis.

Author

Yatomi, Masakiyo, Akasaka, Keiichi, Sato, Shintaro, Chida, Mizuki, Kanbe, Mio, Sawada, Hiru, Yokota, Itaru, Wakamatsu, Ikuo, Muto, Sohei, Sato, Mari, Yamaguchi, Kochi, Miura, Yosuke, Tsurumaki, Hiroaki, Sakurai, Reiko, Hara, Kenichiro, Koga, Yasuhiko, Sunaga, Noriaki, Yamakawa, Hideaki, Matsushima, Hidekazu, and Yamazaki, Sahori

Subjects
PULMONARY alveolar proteinosis, PULMONARY fibrosis, DERMATOMYOSITIS, BRONCHOALVEOLAR lavage, RESPIRATORY insufficiency, GRANULOCYTE-macrophage colony-stimulating factor, LUNG diseases
Abstract

Background: Autoimmune pulmonary alveolar proteinosis (APAP) is a diffuse lung disease that causes abnormal accumulation of lipoproteins in the alveoli; however, its pathogenesis remains unclear. Recently, APAP cases have been reported during the course of dermatomyositis. The combination of these two diseases may be coincidental; however, it may have been overlooked because differentiating APAP from a flare-up of interstitial pneumonia associated with dermatomyositis is challenging. This didactic case demonstrates the need for early APAP scrutiny. Case presentation: A 50-year-old woman was diagnosed with anti-melanoma differentiation-associated gene 5 (anti-MDA5) antibody-positive dermatitis and interstitial pneumonia in April 2021. The patient was treated with corticosteroids, tacrolimus, and cyclophosphamide pulse therapy for interstitial pneumonia complicated by MDA5 antibody-positive dermatitis, which improved the symptoms and interstitial pneumonia. Eight months after the start of treatment, a new interstitial shadow appeared that worsened. Therefore, three additional courses of cyclophosphamide pulse therapy were administered; however, the respiratory symptoms and interstitial shadows did not improve. Respiratory failure progressed, and 14 months after treatment initiation, bronchoscopy revealed turbid alveolar lavage fluid, numerous foamy macrophages, and numerous periodic acid–Schiff-positive unstructured materials. Blood test results revealed high anti-granulocyte–macrophage colony-stimulating factor (GM-CSF) antibody levels, leading to a diagnosis of APAP. The patient underwent whole-lung lavage, and the respiratory disturbance promptly improved. Anti-GM-CSF antibodies were measured from the cryopreserved serum samples collected at the time of diagnosis of anti-MDA5 antibody-positive dermatitis, and 10 months later, both values were significantly higher than normal. Conclusions: This is the first report of anti-MDA5 antibody-positive dermatomyositis complicated by interstitial pneumonia with APAP, which may develop during immunosuppressive therapy and be misdiagnosed as a re-exacerbation of interstitial pneumonia. In anti-MDA5 antibody-positive dermatomyositis, APAP comorbidity may have been overlooked, and early evaluation with bronchoalveolar lavage fluid and anti-GM-CSF antibody measurements should be considered, keeping the development of APAP in mind. [ABSTRACT FROM AUTHOR]

Published
2024
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17. Gender differences on preoperative psychologic factors affecting acute postoperative pain in patients with lumbar spinal disorders

Author

Watanabe, Yuki, primary, Nikaido, Takuya, additional, Yabuki, Shoji, additional, Abe, Jumpei, additional, Suzuki, Hideki, additional, Shishido, Keita, additional, Kobayashi, Hirotaka, additional, Yoshida, Rii, additional, Iinuma, Kaori, additional, Nagamine, Sakiko, additional, Ono, Yoko, additional, Sato, Mari, additional, and Oi, Naoyuki, additional

Published
2023
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18. 12-Lipoxygenase Regulates Cold Adaptation and Glucose Metabolism by Producing the Omega-3 Lipid 12-HEPE from Brown Fat

Author

Leiria, Luiz Osório, Wang, Chih-Hao, Lynes, Matthew D., Yang, Kunyan, Shamsi, Farnaz, Sato, Mari, Sugimoto, Satoru, Chen, Emily Y., Bussberg, Valerie, Narain, Niven R., Sansbury, Brian E., Darcy, Justin, Huang, Tian Lian, Kodani, Sean D., Sakaguchi, Masaji, Rocha, Andréa L., Schulz, Tim J., Bartelt, Alexander, Hotamisligil, Gökhan S., Hirshman, Michael F., van Leyen, Klaus, Goodyear, Laurie J., Blüher, Matthias, Cypess, Aaron M., Kiebish, Michael A., Spite, Matthew, and Tseng, Yu-Hua

Published
2019
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20. Chopart amputation with tendon balancing

Author

Ouchi, Kazuo, Oi, Naoyuki, Sato, Mari, Yabuki, Shoji, and Konno, Shin-Ichi

Subjects
tendon balancing, foot prosthesis, General Medicine, Chopart amputation
Abstract

Background: When foot necrosis occurs due to lower limb blood flow disorder caused by diabetes or peripheral arterial occlusion, many patients require lower limb amputation. The functional prognosis after lower limb amputation largely depends on whether the heel can be preserved. However, there are many reports that Chopart amputation causes varus and equinus deformity, and is functionally unfavorable. We herein report a case of Chopart amputation performed with muscle balancing. Postoperatively, the foot was not deformed and the patient was able to walk independently with a foot prosthesis. Case: A 78-year-old man presented with ischemic necrosis of his right forefoot. The range of necrosis extended to the central part of the sole, so Chopart amputation was performed. In the operation, to prevent varus and equinus deformity, the Achilles tendon was lengthened, the tibialis anterior tendon was transferred through a tunnel created in the neck of talus, and the peroneus brevis tendon was transferred through a tunnel created in the anterior part of the calcaneus. At the final follow-up 7 years after the operation, no varus or equinus deformity was observed. The patient became able to stand up and walk on his heel without a prosthesis. In addition, step motion was possible by wearing a foot prosthesis.

Published
2023

25. Effective treatment with mepolizumab in a patient with severe eosinophilic granulomatosis with polyangiitis complicated with small intestine perforation

Author

Sato, Mari, primary, Yatomi, Masakiyo, additional, Wakamatsu, Ikuo, additional, Uno, Shogo, additional, Hanazato, Chiharu, additional, Masuda, Tomomi, additional, Yamaguchi, Koichi, additional, Aoki-Saito, Haruka, additional, Kasahara, Norimitsu, additional, Miura, Yosuke, additional, Tsurumaki, Hiroaki, additional, Hara, Kenichiro, additional, Koga, Yasuhiko, additional, Sunaga, Noriaki, additional, Okada, Takuhisa, additional, Ikota, Hayato, additional, Hisada, Takeshi, additional, and Maeno, Toshitaka, additional

Published
2023
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27. Sustained antitumor response to lenvatinib with weekend-off and alternate-day administration in chemotherapy-refractory thymic carcinoma: a case report

Author

Sunaga, Noriaki, primary, Miura, Yosuke, additional, Sakurai, Reiko, additional, Ohshima, Sohei, additional, Uno, Shogo, additional, Muto, Sohei, additional, Sato, Mari, additional, Tsurumaki, Hiroaki, additional, Yatomi, Masakiyo, additional, Koga, Yasuhiko, additional, Ohtaki, Yoichi, additional, Nagashima, Toshiteru, additional, Okano, Naoko, additional, Kubo, Nobuteru, additional, Maeno, Toshitaka, additional, and Hisada, Takeshi, additional

Published
2022
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30. Relationship between dysphagia and motor function in community‐dwelling older people.

Author

Sato, Mari, Tominaga, Ryoji, Kurita, Noriaki, Sekiguchi, Miho, Otani, Koji, Konno, Shin‐ichi, and Oi, Naoyuki

Subjects
*GRIP strength, *DEGLUTITION disorders, *INDEPENDENT living, *DESCRIPTIVE statistics, *LOGISTIC regression analysis, *ODDS ratio, *MOTOR ability, *EARLY diagnosis
Abstract

Aim: Dysphagia is a problem typically associated with aging. The aim was to investigate the relationship between dysphagia and motor function using a simple assessment method that can be performed in the community setting, and to promote the early detection and prevention of dysphagia. Methods: Data from the Locomotive Syndrome and Health Outcome in Aizu Cohort Study (LOHAS) were used. Those aged ≥65 years were included. Motor function was assessed using a grip strength test, single limb standing test (SLS), and timed up and go test (TUG). Swallowing function was assessed using the Japanese version of the 10‐item Eating Assessment Tool (EAT‐10). The association between motor function and swallowing function was analyzed. Results: In total, 1732 participants were included. In logistic regression modes in which grip strength, SLS, and TUG results were included separately, the odds ratio for dysphagia increased by 1.08 (P = 0.001) for each 1‐kg decrease in grip strength, and increased by 1.15 (P < 0.001) for each 1‐s increase in TUG time. No association was found for SLS. In the model in which grip strength and TUG were included simultaneously, the odds ratio for dysphagia increased by 1.06 (P = 0.01) in grip strength, and increased by 1.11 (P = 0.009) in TUG time. Conclusion: Our results suggest that skeletal muscle strength and dynamic balance function are associated with dysphagia in community‐dwelling older people. Geriatr Gerontol Int 2023; 23: 603–608. [ABSTRACT FROM AUTHOR]

Published
2023
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32. Durable response to afatinib rechallenge in a long‐term survivor of non‐small cell lung cancer harboring EGFR L858R and L747V mutations

Author

Kanbe, Mio, primary, Sunaga, Noriaki, additional, Hara, Kenichiro, additional, Sawada, Hiiru, additional, Wakamatsu, Ikuo, additional, Hara, Kentaro, additional, Muto, Sohei, additional, Sawada, Yuri, additional, Masubuchi, Hiroaki, additional, Sato, Mari, additional, Miura, Yosuke, additional, Tsurumaki, Hiroaki, additional, Yatomi, Masakiyo, additional, Sakurai, Reiko, additional, Koga, Yasuhiko, additional, Ohtaki, Yoichi, additional, Nagashima, Toshiteru, additional, Okano, Naoko, additional, Kubo, Nobuteru, additional, Maeno, Toshitaka, additional, and Hisada, Takeshi, additional

Published
2022
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49. Immune-related adverse events caused by treatment with pembrolizumab in a patient with lung cancer who infected influenza virus

Author

Takemura, Masao, primary, Motegi, Mitsuru, additional, Kuroiwa, Yuya, additional, Itai, Miki, additional, Taguchi, Kohei, additional, Umetsu, Kazue, additional, Uchida, Megumi, additional, Kouno, Shunichi, additional, Sato, Mari, additional, Masubuchi, Hiroaki, additional, Yamaguchi, Aya, additional, Yamaguchi, Koichi, additional, Ikeda, Kana, additional, Nakagawa, Junichi, additional, and Maeno, Toshitaka, additional

Published
2021
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