Meyer S, Turina T, Schumacher H G, Weigand K
Innere Abteilung, Schwerpunkt Gastroenterologie, Kreiskrankenhaus Schwäbisch Gmünd in Mutlangen.
Dtsch Med Wochenschr. 1988 Jun 24;113(25):1022-4. doi: 10.1055/s-2008-1067761.
Surgery was required for a 23-year-old woman with rapidly progressive reduction in liver function and treatment-resistant ascites due to Budd-Chiari syndrome. A dorsocranial liver resection with hepatoatrial anastomosis was performed. The postoperative course has been satisfactory, demonstrating that this method should be seriously considered in the treatment of Budd-Chiari syndrome.
一名23岁女性因布加综合征导致肝功能迅速恶化且腹水难治,需要进行手术。实施了经颅肝切除术并进行肝房吻合术。术后过程令人满意,表明该方法在布加综合征的治疗中应予以认真考虑。