ダウンロード数: 2084
このアイテムのファイル:
ファイル | 記述 | サイズ | フォーマット | |
---|---|---|---|---|
57_193.pdf | 1.32 MB | Adobe PDF | 見る/開く |
タイトル: | 偽性低アルドステロン症Ⅰ型を呈した両側原発性閉塞性巨大尿管症の1例 |
その他のタイトル: | Pseudohypoaldosteronism Type 1 in an Infant with Bilateral Primary Obstructive Megaureter : A Case Report |
著者: | 牧野, 雄樹 兼松, 明弘 今村, 正明 吉村, 耕治 西山, 博之 依藤, 亨 小川, 修 |
著者名の別形: | Makino, Yuki Kanematsu, Akihiro Imamura, Masaaki Yoshimura, Koji Nishiyama, Hiroyuki Yorifuji, Tohru Ogawa, Osamu |
キーワード: | Pseudohypoaldosteronism Megaureter |
発行日: | Apr-2011 |
出版者: | 泌尿器科紀要刊行会 |
誌名: | 泌尿器科紀要 |
巻: | 57 |
号: | 4 |
開始ページ: | 193 |
終了ページ: | 197 |
抄録: | A 35-day-old male infant was referred to our hospital for bilateral hydroureteronephrosis on postnatal ultrasonography. He was born at 37 weeks and 2 days of gestation, weighing 2, 765 g. He was diagnosed with bilateral primary obstructive megaureter. During observation, at 3 months and 2 weeks of age, he presented with dehydration and showed hyponatremia and hyperkalemia. An endocrinological examination led to a diagnosis of pseudohypoaldosteronism type 1 (PHA1). After bilateral percutaneous nephrostomy, PHA1 resolved. He underwent bilateral ureteral tapering and ureteroneocystostomy at 5 months and 3 weeks of age. Since PHA1 recurred after removal of urethral catheter, urethral catheter and bilateral double-J-stent was kept until 8 months old. He was followed-up until 3 years old with no signs of PHA1 recurrence. For an infant with obstructive uropathy or vesicoureteral reflux showing hyponatremia and hyperkalemia, PHA1 should be considered. |
著作権等: | 許諾条件により本文は2012-05-01に公開 |
URI: | http://hdl.handle.net/2433/141824 |
PubMed ID: | 21646850 |
出現コレクション: | Vol.57 No.4 |
このリポジトリに保管されているアイテムはすべて著作権により保護されています。