過誤腫性ポリポーシスの診断と治療

Naoki Ohmiya, Masanao Nakamura, Tomoyuki Shibata

研究成果: ジャーナルへの寄稿学術論文査読

1 被引用数 (Scopus)

抄録

The hamartomatous polyposis syndromes are a group of inherited disorders that include Peutz-Jeghers syndrome (PJS), juvenile polyposis syndrome, Cowden syndrome, and tuberous sclerosis complex (TSC). PJS, Cowden syndrome, and TSC are characterized by phenotypic manifestations, which may be a clue to their diagnosis. The most frequent complications of PJS are intussusception and chronic anemia. Earlier entire small bowel examination with capsule endoscopy and balloon-assisted enteroscopy enabling accurate diagnosis and subsequent endoscopic polyp removal obviates the need for unnecessary multiple surgeries. Patients with a hamartomatous polyposis syndrome are at an elevated risk for gastrointestinal and extragastrointestinal malignancies; therefore periodic surveillance is needed. Here, we describe the clinical features, diagnostics, and therapeutics of hamartomatous polyposis syndromes.

寄稿の翻訳タイトルDiagnosis and treatment of hamartomatous polyposis syndromes
本文言語日本語
ページ(範囲)1323-1335
ページ数13
ジャーナルGASTROENTEROLOGICAL ENDOSCOPY
63
7
DOI
出版ステータス出版済み - 2021

All Science Journal Classification (ASJC) codes

  • 放射線学、核医学およびイメージング
  • 消化器病学

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