医学部 小児科学講座

田島 敏広

タジマ トシヒロ  (Toshihiro Tajima)

基本情報

所属
自治医科大学 附属病院 とちぎ子ども医療センター小児科
学位
博士(医学)(北海道大学)

J-GLOBAL ID
200901003645122426
researchmap会員ID
5000045642

論文

 151
  • Keisuke Nagasaki, Kanshi Minamitani, Akie Nakamura, Hironori Kobayashi, Chikahiko Numakura, Masatsune Itoh, Yuichi Mushimoto, Kaori Fujikura, Masaru Fukushi, Toshihiro Tajima
    Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology 32(1) 26-51 2023年  
    Purpose of developing the guidelines: Newborn screening (NBS) for congenital hypothyroidism (CH) was started in 1979 in Japan, and early diagnosis and treatment improved the intelligence prognosis of CH patients. The incidence of CH was once about one in 5,000-8,000 births, but has been increased with diagnosis of subclinical CH. The disease requires continuous treatment and specialized medical facilities should conduct differential diagnosis and treatment in patients who are positive by NBS to avoid unnecessary treatment. The Guidelines for Mass Screening of Congenital Hypothyroidism (1998 version) were developed by the Mass Screening Committee of the Japanese Society for Pediatric Endocrinology in 1998. Subsequently, the guidelines were revised in 2014. Here, we have added minor revisions to the 2014 version to include the most recent findings. Target disease/conditions: Primary congenital hypothyroidism. Users of the Guidelines: Physician specialists in pediatric endocrinology, pediatric specialists, physicians referring pediatric practitioners, general physicians, laboratory technicians in charge of mass screening, and patients.
  • Tomohiro Ishii, Kenichi Kashimada, Naoko Amano, Kei Takasawa, Akari Nakamura-Utsunomiya, Shuichi Yatsuga, Tokuo Mukai, Shinobu Ida, Mitsuhisa Isobe, Masaru Fukushi, Hiroyuki Satoh, Kaoru Yoshino, Michio Otsuki, Takuyuki Katabami, Toshihiro Tajima
    Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology 31(3) 116-143 2022年  
    Congenital adrenal hyperplasia is a category of disorders characterized by impaired adrenocortical steroidogenesis. The most frequent disorder of congenital adrenal hyperplasia is 21-hydroxylase deficiency, which is caused by pathogenic variants of CAY21A2 and is prevalent between 1 in 18,000 and 20,000 in Japan. The clinical guidelines for 21-hydroxylase deficiency in Japan have been revised twice since a diagnostic handbook in Japan was published in 1989. On behalf of the Japanese Society for Pediatric Endocrinology, the Japanese Society for Mass Screening, the Japanese Society for Urology, and the Japan Endocrine Society, the working committee updated the guidelines for the diagnosis and treatment of 21-hydroxylase deficiency published in 2014, based on recent evidence and knowledge related to this disorder. The recommendations in the updated guidelines can be applied in clinical practice considering the risks and benefits to each patient.
  • 棚橋 祐典, 伊藤 純子, 島津 章, 高野 幸路, 田島 敏広, 羽二生 邦彦, 堀川 玲子, 松井 克之, 松野 彰, 村上 信行, 望月 貴博, 横谷 進, 依藤 亨, 石井 智弘, 長谷川 奉延, 成長科学協会成長ホルモン治療専門員会
    日本内分泌学会雑誌 97(2) 561-561 2021年10月  
  • 田島 敏広, 小熊 真紀子
    日本内分泌学会雑誌 97(2) 564-564 2021年10月  

MISC

 21

共同研究・競争的資金等の研究課題

 8