학술논문
A case of polysplenia syndrome and preduodenal portal vein/ common bile duct with choledocholithiasis / 胆石総胆管結石を合併した多脾症候群・十二指腸前門脈総胆管・左側胆嚢の1例
Document Type
Journal Article
Author
Hiroyasu MAKUUCHI; Hiroyuki KASHIWAGI; Kenichi OKADA; Kosuke TOBITA; Masahiro MATSUYAMA; Masanori ISHII; Naoki YAZAWA; Shoichi DOWAKI; Takafumi SEKKA; Toshihide IMAIZUMI; Yasuhisa OIDA; Yasuo OHTANI; Yoshinori SUGIO; Yosio IWATA; 今泉 俊秀; 堂脇 昌一; 大谷 泰雄; 岡田 健一; 岩田 美郎; 幕内 博康; 杉尾 芳紀; 松山 正浩; 柏木 宏之; 矢澤 直樹; 石井 正紀; 石過 孝文; 種田 靖久; 飛田 浩輔
Source
胆道 / Tando. 2006, 20(2):204
Subject
Language
Japanese
ISSN
0914-0077
1883-6879
1883-6879
Abstract
Polysplenia syndrome is a very rare congenital disease to complicated major cardiovascular anomalies with severe cyanosis and visceral heterotaxia, in almost cases. We reported a case of choledocholithiasis with polysplenia syndrome and preduodenal portal vein and common bile duct in Tetralogy of Fallot (T/F) postoperative 16 years. In May,2000, a 56 years old woman was admitted to our hospital, because of epigastralgia after meal. Past operation histories were Blalock-Taussig operation in 34 years ago and radical operation in 16 years ago for T/F. And there were several times hospitalization for heart failure treatment. As a result of inspection after hospitalization, polysplenia, the absence of the hepatic portion of the inferior vena cava and azygos continuation of right IVC, the left-side gall bladder, intestinal malrotation, preduodenal portal vein and common bile duct were pointed out. After evaluation of a careful cardio-pulmonary function, operation was performed. We confirmed the above-mentioned anomalies and cholecystectomy and choledocholithotomy were enforced. In postoperative 14 days, she discharged uneventfully.