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Your search keyword '"Hattori, Yukinori"' showing total 14 results
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14 results on '"Hattori, Yukinori"'

3. Malignant gastrointestinal neuroectodermal tumor presenting with small intestinal obstruction: A case report

Author

Sasaki, Makiko, primary, Tanaka, Mamoru, additional, Asukai, Koki, additional, Koguchi, Hiroki, additional, Inoue, Yusuke, additional, Moriyama, Mizuki, additional, Tsukahara, Tetsuo, additional, Kawahara, Takeo, additional, Hayashi, Eiji, additional, Hattori, Yukinori, additional, Hasegawa, Izumi, additional, and Kataoka, Hiromi, additional

Published
2022
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4. A Japanese female with chronic mild anemia and primary iron overloading disease

Author

Hattori, Yukinori, Kato, Hiroyuki, Kato, Ayako, Tatsumi, Yasuaki, Kato, Koichi, and Hayashi, Hisao

Subjects
congestive heart failure, cirrhosis, diabetes mellitus, iron overload, anemia
Abstract

A 65-year-old woman died of congestive heart failure and diabetes mellitus. She had a history of mild anemia since adolescence, but received neither iron supplementation nor transfusion. The cirrhotic liver obtained at autopsy contained a large amount of iron. The heart and pancreas also had excess iron. Her iron overload may be due to excess iron absorption in the gut because of the absence of an iatrogenic background such as transfusion or iron supplementation.

Published
2020

14. [Sudden death associated with myocardial damage caused by microthrombi in a patient with thrombotic thrombocytopenic purpura].

Author

Yamamoto K, Hattori Y, Shimada K, Araki Y, Adachi T, and Tsushita K

Subjects
Adult, Autopsy, Female, Humans, Cardiomyopathies complications, Death, Sudden etiology, Purpura, Thrombotic Thrombocytopenic complications, Thrombosis complications
Abstract

We describe a 35-year-old woman with Down's syndrome who was admitted to a clinic with anorexia and vomiting. Since laboratory findings showed anemia (Hb 7.4 g/dl) and thrombocytopenia (0.5 × 10⁴/μl), she was transferred to our hospital for treatment. Further laboratory examinations revealed schistocytes, LDH elevation, and a negative Coombs' test. Thrombotic thrombocytopenic purpura (TTP) was suspected. Plasma exchange (PEX) and prednisolone administration were thus immediately initiated. Prior to these treatments, ADAMTS13 activity was less than 5% and inhibitors were detected at a level of 0.8 Bethesda U/ml. Although her platelet count had risen to 13.0 × 10⁴/μl by day 6 (post 4 sessions of PEX), it had decreased to 1.8 × 10⁴/μl on day 7. Despite ongoing PEX, thrombocytopenia persisted. On day 21, she suddenly died. Autopsy findings revealed no evidence of myocardial necrosis or coronary artery thrombosis. Extensive microthrombi were, however, detected in precapillary arterioles, capillaries, and post-capillary venules of the heart. Therefore, this patient's sudden death was clinically suspected to have been caused by cardiomyopathy, which had produced cardiogenic shock.

Published
2015
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