The Experts below are selected from a list of 17874 Experts worldwide ranked by ideXlab platform
Youhei Marukawa - One of the best experts on this subject based on the ideXlab platform.
-
immunoglobulin g4 related periaortitis complicated by Aortic Rupture and aortoduodenal fistula after endovascular aaa repair
Journal of Endovascular Therapy, 2014Co-Authors: Satomi Kasashima, Atsuhiro Kawashima, Fuminori Kasashima, Masamitsu Endo, Yasushi Matsumoto, Kengo Kawakami, Masato Kayahara, Hajime Ohta, Masaaki Yano, Youhei MarukawaAbstract:Purpose:To report a rare and complicated case of immunoglobulin (Ig) G4-related periaortitis involving both the Aortic wall and the retroperitoneum without aneurysmal formation.Case Report:A 79-year-old man with IgG4-related periaortitis suffered Aortic Rupture despite a normal caliber aorta after 6 months of steroid therapy (20 mg/d). Endovascular repair with an Aortic cuff sealed the Rupture. Steroid therapy was halted 2 weeks later due to infection. Four months later, a biopsy during esophagogastroduodenoscopy to investigate gastrointestinal bleeding suggested a relapse of IgG4-RD in the duodenum. Subsequent aortoduodenal fistula formation proved fatal. Generally, IgG4-related periaortitis does not result in such complications due to the absence of aneurysm formation and a thick Aortic wall.Conclusions:Our report highlights a rare case of IgG4-related periaortitis where complications resulted following steroid therapy and surgical intervention, emphasizing the difficulties in dealing with IgG4-related ...
-
immunoglobulin g4 related periaortitis complicated by Aortic Rupture and aortoduodenal fistula after endovascular aaa repair
Journal of Endovascular Therapy, 2014Co-Authors: Satomi Kasashima, Atsuhiro Kawashima, Fuminori Kasashima, Masamitsu Endo, Yasushi Matsumoto, Kengo Kawakami, Masato Kayahara, Hajime Ohta, Masaaki Yano, Youhei MarukawaAbstract:Purpose To report a rare and complicated case of immunoglobulin (Ig) G4-related periaortitis involving both the Aortic wall and the retroperitoneum without aneurysmal formation. Case report A 79-year-old man with IgG4-related periaortitis suffered Aortic Rupture despite a normal caliber aorta after 6 months of steroid therapy (20 mg/d). Endovascular repair with an Aortic cuff sealed the Rupture. Steroid therapy was halted 2 weeks later due to infection. Four months later, a biopsy during esophagogastroduodenoscopy to investigate gastrointestinal bleeding suggested a relapse of IgG4-RD in the duodenum. Subsequent aortoduodenal fistula formation proved fatal. Generally, IgG4-related periaortitis does not result in such complications due to the absence of aneurysm formation and a thick Aortic wall. Conclusions Our report highlights a rare case of IgG4-related periaortitis where complications resulted following steroid therapy and surgical intervention, emphasizing the difficulties in dealing with IgG4-related cardiovascular lesions.
Satomi Kasashima - One of the best experts on this subject based on the ideXlab platform.
-
immunoglobulin g4 related periaortitis complicated by Aortic Rupture and aortoduodenal fistula after endovascular aaa repair
Journal of Endovascular Therapy, 2014Co-Authors: Satomi Kasashima, Atsuhiro Kawashima, Fuminori Kasashima, Masamitsu Endo, Yasushi Matsumoto, Kengo Kawakami, Masato Kayahara, Hajime Ohta, Masaaki Yano, Youhei MarukawaAbstract:Purpose:To report a rare and complicated case of immunoglobulin (Ig) G4-related periaortitis involving both the Aortic wall and the retroperitoneum without aneurysmal formation.Case Report:A 79-year-old man with IgG4-related periaortitis suffered Aortic Rupture despite a normal caliber aorta after 6 months of steroid therapy (20 mg/d). Endovascular repair with an Aortic cuff sealed the Rupture. Steroid therapy was halted 2 weeks later due to infection. Four months later, a biopsy during esophagogastroduodenoscopy to investigate gastrointestinal bleeding suggested a relapse of IgG4-RD in the duodenum. Subsequent aortoduodenal fistula formation proved fatal. Generally, IgG4-related periaortitis does not result in such complications due to the absence of aneurysm formation and a thick Aortic wall.Conclusions:Our report highlights a rare case of IgG4-related periaortitis where complications resulted following steroid therapy and surgical intervention, emphasizing the difficulties in dealing with IgG4-related ...
-
immunoglobulin g4 related periaortitis complicated by Aortic Rupture and aortoduodenal fistula after endovascular aaa repair
Journal of Endovascular Therapy, 2014Co-Authors: Satomi Kasashima, Atsuhiro Kawashima, Fuminori Kasashima, Masamitsu Endo, Yasushi Matsumoto, Kengo Kawakami, Masato Kayahara, Hajime Ohta, Masaaki Yano, Youhei MarukawaAbstract:Purpose To report a rare and complicated case of immunoglobulin (Ig) G4-related periaortitis involving both the Aortic wall and the retroperitoneum without aneurysmal formation. Case report A 79-year-old man with IgG4-related periaortitis suffered Aortic Rupture despite a normal caliber aorta after 6 months of steroid therapy (20 mg/d). Endovascular repair with an Aortic cuff sealed the Rupture. Steroid therapy was halted 2 weeks later due to infection. Four months later, a biopsy during esophagogastroduodenoscopy to investigate gastrointestinal bleeding suggested a relapse of IgG4-RD in the duodenum. Subsequent aortoduodenal fistula formation proved fatal. Generally, IgG4-related periaortitis does not result in such complications due to the absence of aneurysm formation and a thick Aortic wall. Conclusions Our report highlights a rare case of IgG4-related periaortitis where complications resulted following steroid therapy and surgical intervention, emphasizing the difficulties in dealing with IgG4-related cardiovascular lesions.
Kengo Kawakami - One of the best experts on this subject based on the ideXlab platform.
-
immunoglobulin g4 related periaortitis complicated by Aortic Rupture and aortoduodenal fistula after endovascular aaa repair
Journal of Endovascular Therapy, 2014Co-Authors: Satomi Kasashima, Atsuhiro Kawashima, Fuminori Kasashima, Masamitsu Endo, Yasushi Matsumoto, Kengo Kawakami, Masato Kayahara, Hajime Ohta, Masaaki Yano, Youhei MarukawaAbstract:Purpose:To report a rare and complicated case of immunoglobulin (Ig) G4-related periaortitis involving both the Aortic wall and the retroperitoneum without aneurysmal formation.Case Report:A 79-year-old man with IgG4-related periaortitis suffered Aortic Rupture despite a normal caliber aorta after 6 months of steroid therapy (20 mg/d). Endovascular repair with an Aortic cuff sealed the Rupture. Steroid therapy was halted 2 weeks later due to infection. Four months later, a biopsy during esophagogastroduodenoscopy to investigate gastrointestinal bleeding suggested a relapse of IgG4-RD in the duodenum. Subsequent aortoduodenal fistula formation proved fatal. Generally, IgG4-related periaortitis does not result in such complications due to the absence of aneurysm formation and a thick Aortic wall.Conclusions:Our report highlights a rare case of IgG4-related periaortitis where complications resulted following steroid therapy and surgical intervention, emphasizing the difficulties in dealing with IgG4-related ...
-
immunoglobulin g4 related periaortitis complicated by Aortic Rupture and aortoduodenal fistula after endovascular aaa repair
Journal of Endovascular Therapy, 2014Co-Authors: Satomi Kasashima, Atsuhiro Kawashima, Fuminori Kasashima, Masamitsu Endo, Yasushi Matsumoto, Kengo Kawakami, Masato Kayahara, Hajime Ohta, Masaaki Yano, Youhei MarukawaAbstract:Purpose To report a rare and complicated case of immunoglobulin (Ig) G4-related periaortitis involving both the Aortic wall and the retroperitoneum without aneurysmal formation. Case report A 79-year-old man with IgG4-related periaortitis suffered Aortic Rupture despite a normal caliber aorta after 6 months of steroid therapy (20 mg/d). Endovascular repair with an Aortic cuff sealed the Rupture. Steroid therapy was halted 2 weeks later due to infection. Four months later, a biopsy during esophagogastroduodenoscopy to investigate gastrointestinal bleeding suggested a relapse of IgG4-RD in the duodenum. Subsequent aortoduodenal fistula formation proved fatal. Generally, IgG4-related periaortitis does not result in such complications due to the absence of aneurysm formation and a thick Aortic wall. Conclusions Our report highlights a rare case of IgG4-related periaortitis where complications resulted following steroid therapy and surgical intervention, emphasizing the difficulties in dealing with IgG4-related cardiovascular lesions.
Masato Kayahara - One of the best experts on this subject based on the ideXlab platform.
-
immunoglobulin g4 related periaortitis complicated by Aortic Rupture and aortoduodenal fistula after endovascular aaa repair
Journal of Endovascular Therapy, 2014Co-Authors: Satomi Kasashima, Atsuhiro Kawashima, Fuminori Kasashima, Masamitsu Endo, Yasushi Matsumoto, Kengo Kawakami, Masato Kayahara, Hajime Ohta, Masaaki Yano, Youhei MarukawaAbstract:Purpose:To report a rare and complicated case of immunoglobulin (Ig) G4-related periaortitis involving both the Aortic wall and the retroperitoneum without aneurysmal formation.Case Report:A 79-year-old man with IgG4-related periaortitis suffered Aortic Rupture despite a normal caliber aorta after 6 months of steroid therapy (20 mg/d). Endovascular repair with an Aortic cuff sealed the Rupture. Steroid therapy was halted 2 weeks later due to infection. Four months later, a biopsy during esophagogastroduodenoscopy to investigate gastrointestinal bleeding suggested a relapse of IgG4-RD in the duodenum. Subsequent aortoduodenal fistula formation proved fatal. Generally, IgG4-related periaortitis does not result in such complications due to the absence of aneurysm formation and a thick Aortic wall.Conclusions:Our report highlights a rare case of IgG4-related periaortitis where complications resulted following steroid therapy and surgical intervention, emphasizing the difficulties in dealing with IgG4-related ...
-
immunoglobulin g4 related periaortitis complicated by Aortic Rupture and aortoduodenal fistula after endovascular aaa repair
Journal of Endovascular Therapy, 2014Co-Authors: Satomi Kasashima, Atsuhiro Kawashima, Fuminori Kasashima, Masamitsu Endo, Yasushi Matsumoto, Kengo Kawakami, Masato Kayahara, Hajime Ohta, Masaaki Yano, Youhei MarukawaAbstract:Purpose To report a rare and complicated case of immunoglobulin (Ig) G4-related periaortitis involving both the Aortic wall and the retroperitoneum without aneurysmal formation. Case report A 79-year-old man with IgG4-related periaortitis suffered Aortic Rupture despite a normal caliber aorta after 6 months of steroid therapy (20 mg/d). Endovascular repair with an Aortic cuff sealed the Rupture. Steroid therapy was halted 2 weeks later due to infection. Four months later, a biopsy during esophagogastroduodenoscopy to investigate gastrointestinal bleeding suggested a relapse of IgG4-RD in the duodenum. Subsequent aortoduodenal fistula formation proved fatal. Generally, IgG4-related periaortitis does not result in such complications due to the absence of aneurysm formation and a thick Aortic wall. Conclusions Our report highlights a rare case of IgG4-related periaortitis where complications resulted following steroid therapy and surgical intervention, emphasizing the difficulties in dealing with IgG4-related cardiovascular lesions.
Hajime Ohta - One of the best experts on this subject based on the ideXlab platform.
-
immunoglobulin g4 related periaortitis complicated by Aortic Rupture and aortoduodenal fistula after endovascular aaa repair
Journal of Endovascular Therapy, 2014Co-Authors: Satomi Kasashima, Atsuhiro Kawashima, Fuminori Kasashima, Masamitsu Endo, Yasushi Matsumoto, Kengo Kawakami, Masato Kayahara, Hajime Ohta, Masaaki Yano, Youhei MarukawaAbstract:Purpose:To report a rare and complicated case of immunoglobulin (Ig) G4-related periaortitis involving both the Aortic wall and the retroperitoneum without aneurysmal formation.Case Report:A 79-year-old man with IgG4-related periaortitis suffered Aortic Rupture despite a normal caliber aorta after 6 months of steroid therapy (20 mg/d). Endovascular repair with an Aortic cuff sealed the Rupture. Steroid therapy was halted 2 weeks later due to infection. Four months later, a biopsy during esophagogastroduodenoscopy to investigate gastrointestinal bleeding suggested a relapse of IgG4-RD in the duodenum. Subsequent aortoduodenal fistula formation proved fatal. Generally, IgG4-related periaortitis does not result in such complications due to the absence of aneurysm formation and a thick Aortic wall.Conclusions:Our report highlights a rare case of IgG4-related periaortitis where complications resulted following steroid therapy and surgical intervention, emphasizing the difficulties in dealing with IgG4-related ...
-
immunoglobulin g4 related periaortitis complicated by Aortic Rupture and aortoduodenal fistula after endovascular aaa repair
Journal of Endovascular Therapy, 2014Co-Authors: Satomi Kasashima, Atsuhiro Kawashima, Fuminori Kasashima, Masamitsu Endo, Yasushi Matsumoto, Kengo Kawakami, Masato Kayahara, Hajime Ohta, Masaaki Yano, Youhei MarukawaAbstract:Purpose To report a rare and complicated case of immunoglobulin (Ig) G4-related periaortitis involving both the Aortic wall and the retroperitoneum without aneurysmal formation. Case report A 79-year-old man with IgG4-related periaortitis suffered Aortic Rupture despite a normal caliber aorta after 6 months of steroid therapy (20 mg/d). Endovascular repair with an Aortic cuff sealed the Rupture. Steroid therapy was halted 2 weeks later due to infection. Four months later, a biopsy during esophagogastroduodenoscopy to investigate gastrointestinal bleeding suggested a relapse of IgG4-RD in the duodenum. Subsequent aortoduodenal fistula formation proved fatal. Generally, IgG4-related periaortitis does not result in such complications due to the absence of aneurysm formation and a thick Aortic wall. Conclusions Our report highlights a rare case of IgG4-related periaortitis where complications resulted following steroid therapy and surgical intervention, emphasizing the difficulties in dealing with IgG4-related cardiovascular lesions.