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Stephen C. Brown MMeD FCP DCH Marc Gewillig MD PhD 《Catheterization and cardiovascular interventions》2010,75(3):416-419
We report a complication related to advancement of a large diameter long sheath in the obturator vein. In an adult with a previously thrombosed femoral vein, the obturator vein was inadvertently cannulated. During percutaneous pulmonary valve implantation, the Ensemble® delivery system could not be advanced after repositioning attempt. The obturator vein had been perforated and sheath was coiled up in the pelvis leading to a retroperitoneal pelvic hematoma. Continuity of the vein was established using two self‐expanding covered stents. The obturator vein runs dorsally and joins the inferior caval vein at a very acute angle posterior in the pelvis, creating a corner in which stiff catheters or sheaths may get entrapped. © 2009 Wiley‐Liss, Inc. 相似文献
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Eman Hamid MD Kigocha Okengo MSc Biniyam A. Ayele MD Daniel Gams Massi MD Samia Ben Sassi MD Houyam Tibar MD Sarah Misbah El-Sadig MD MRCP FRCP Soulaimane Mahoui MDDCh Julien Razafimahefa MD MSc Ange Eric Kouame-Assouan MD Djibrilla Ben-Adji MD Lengane Y.T. Modeste MD Muhyadin Hassan Mohamed MBBCh MSc. MHSM Nestor Nsengiyumva MD Wael Abdulgader Alwahchi MBSS Saara Ndinelago Neshuku MBChB FCN MMED Neurology Cassandra Ocampo MD Foksouna Sakadi MD João Bilardo Caiano MD Antonia Rodrigues Fortes MSc Maouly Fall MD Gift Wilson Ngwende MBChB MMed FEBN Juzar Hooker MB ChB MMeD DCN FCP Augustina Charway-Felli MD PhD Masharip Atadzhanov MD PhD MSc Jonathan Carr PhD MBCHB Njideka U. Okubadejo MBCHB MD FMCP Ali Shalash MD PhD 《Movement disorders》2023,38(2):178-184
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Liyuan Xu MMeD Hongju Zhang MD Guowen Liu MMeD Yunpeng Li MD Di Li MMeD Ning Ma MD 《Echocardiography (Mount Kisco, N.Y.)》2023,40(1):57-60
Abernethy malformation, also known as congenital extrahepatic shunt, is a rare anomaly, which is characterized by partial or complete diversion of the portal blood into the systemic venous circulation. The clinical manifestations of Abernethy malformation during childhood include neonatal cholestasis, failure to thrive, mental retardation, and other congenital defects. We report a case of Abernethy malformation Type II in a 9-year-old boy, whose left ventricle was slightly enlarged because of several major aortopulmonary collateral arteries (MAPCAs) but laboratory examinations were normal 5 years earlier. The characteristics of congenital heart disease in patients with Abernethy malformation are discussed. We propose that physicians should be aware of the possibility of Abernethy malformation in children with enlargement of the left ventricular due to systemic-pulmonary collateral circulation. 相似文献
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