Updated on 2025/09/12

写真a

 
ISHII RYU
 
Affiliation
Nippon Medical School Hospital, Department of Pediatrics, Assistant Professor
Title
Assistant Professor
External link

Papers

  • Accurate Diagnosis of Familial Mediterranean Fever Improved Quality of Life for a Patient and Her Family: A Case Report.

    Mami Kurihara, Toru Igarashi, Ryu Ishii, Hanako Tajima, Jun Hayakawa, Makoto Migita

    Journal of Nippon Medical School = Nippon Ika Daigaku zasshi   2025.6

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    Language:English   Publishing type:Research paper (scientific journal)  

    Periodic fever syndrome is diagnosed on the basis of duration of fever, associated symptoms, and blood and genetic test results. During a 6-month period, a 3-year-old girl experienced monthly fever (39°C) episodes persisting 5 to 12 days and two episodes of ankle arthralgia and skin rash during fever. No abdominal or chest pain was noted. Blood tests performed at the time of fever revealed elevated CRP levels and blood sedimentation rates. Urinalysis and bone marrow examination results were unremarkable. Genetic testing for hereditary autoinflammatory disease syndromes showed E84K MEFV gene mutations. After diagnosing atypical familial Mediterranean fever, oral colchicine alleviated the febrile attacks and improved family quality of life. Fever, arthralgia, and skin rash disappeared after oral colchicine, which is effective for atypical familial Mediterranean fever. During the 6 months before the diagnosis, periodic fever disrupted the daily lives of the entire family. The patient was absent from nursery school during fever. The patient's illness affected her mother's health. The mother was concerned about her child's unknown fever, which resulted in depression and the need for psychiatric medication. Colchicine resolved the febrile episodes, and resolution of the patient's symptoms alleviated her mother's depression. This case shows that genetic testing for periodic fever syndrome can improve family quality of life.

    DOI: 10.1272/jnms.JNMS.2025_92-610

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  • 急性腹症の発症を契機に早期診断された交差血管による間欠性水腎症の1例

    石井 龍, 柳原 剛, 高橋 翼, 右田 真, 伊藤 保彦

    日本医科大学医学会雑誌   20 ( 2 )   126 - 129   2024.4

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    Language:Japanese   Publisher:日本医科大学医学会  

    症例は生来健康な8歳男児で、激しい腹痛を主訴とした。血液検査、尿検査、腹部X線、腹部超音波、腹部造影CT各所見より、交差血管による左腎右尿管移行部狭窄症および、それに伴う間欠性水腎症と診断し、絶飲食で維持輸液、鎮痛薬を投与し第3病日に退院した。退院2ヵ月後に左腎優位に排泄遅延を認め、発症8ヵ月にロボット支援下腹腔鏡下左腎盂形成術を行い、術後6ヵ月時で再燃は認めない。本例のように初回の腹痛発作で間欠性水腎症の診断に至った例は極めて稀で、尿検査で潜血を認めたことより腎疾患を疑い、超音波検査、腹部超音波検査により早期診断ができた。

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    Other Link: https://search.jamas.or.jp/default/link?pub_year=2024&ichushi_jid=J04260&link_issn=&doc_id=20240603420008&doc_link_id=%2Fcw1nimed%2F2024%2F002002%2F015%2F0126-0129%26dl%3D0&url=https%3A%2F%2Fwww.medicalonline.jp%2Fjamas.php%3FGoodsID%3D%2Fcw1nimed%2F2024%2F002002%2F015%2F0126-0129%26dl%3D0&type=MedicalOnline&icon=https%3A%2F%2Fjk04.jamas.or.jp%2Ficon%2F00004_2.gif

Misc.

  • 低ALP血症を呈した症例の疾患,病態の後方視的検討

    栗原 茉杏, 田嶋 華子, 石井 龍, 松本 多絵, 上岡 由奈, 秀野 公美, 伊藤 保彦, 右田 真

    日本小児科学会雑誌   128 ( 2 )   374 - 374   2024.2

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    Language:Japanese   Publisher:(公社)日本小児科学会  

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  • BCG接種部の嫌気性菌による蜂窩織炎を契機にWiskott Aldrich症候群と診断された一例

    栗原 茉杏, 早川 潤, 杉原 諄哉, 石井 龍, 上春 光司, 竹下 輝, 楢崎 秀彦, 牛腸 義宏, 右田 真

    日本小児科学会雑誌   127 ( 2 )   367 - 367   2023.2

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    Language:Japanese   Publisher:(公社)日本小児科学会  

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