1.Spontaneous Thrombosis of a Ruptured Deep Femoral Artery Aneurysm
Keiji Iyori ; Yoshitaka Mitsumori ; Kenji Ariizumi ; Ryoichi Hashimoto
Japanese Journal of Cardiovascular Surgery 2013;42(3):204-206
We report a rare case of spontaneous thrombosis of a ruptured deep femoral artery aneurysm. An 85-year-old man presented two days after onset of acute swelling and pain in the left groin. Computed tomography demonstrated rupture of a deep femoral artery aneurysm and thrombosis of the aneurysm. After 1 month of observation, surgical intervention was performed as the local pain persisted. Opening of the aneurysm sac confirmed that thrombosis was complete. Simple ligation and drainage of the aneurysmal sac was performed. His postoperative course was uneventful.
2.Surgical Treatment of a Patient with Aorto-pulmonary Fistula due to Thoracic Aortic Aneurysm Rupture Associated with Gastric Carcinoma.
Shinya Motohashi ; Shunya Shindo ; Kenji Kubota ; Atsuo Kojima ; Tadao Ishimoto ; Keiji Iyori ; Masahiro Kobayashi ; Yusuke Tada
Japanese Journal of Cardiovascular Surgery 2001;30(5):265-267
A 57-year-old man suffered hemoptysis during an examination for gastric carcinoma. Enhanced computed tomography demonstrated rupture of a thoracic aortic aneurysm to the left pulmonary lower lobe. The lateral segment of the liver was atrophic due to intrahepatic cholelithiasis. Emergency operation was performed after he was transferred to our hospital. The thoracic aorta was reconstructed using a temporary bypass and the pulmonary left lower lobe was resected. The omentum was mobilized and used to cover the prosthesis and bronchial stump. The gastric carcinoma and intrahepatic cholelithiasis with biliary stones in the common bile duct were treated in the next procedure. The pathologic examination revealed lymph node metastasis; thus this operation was recognized to be absolutely noncurative. The treatment of cardiovascular disease concomitant with malignancy remains controversial. The strategy to treat such patients is discussed in this report.
3.A Case of Celiac Artery Aneurysm with Type IIIb Aortic Dissection.
Harunobu Matsumoto ; Shunya Shindo ; Okihiko Akashi ; Kenji Kubota ; Atsuo Kojima ; Tadao Ishimoto ; Kenji Iyori ; Masahiro Kobayashi ; Yusuke Tada
Japanese Journal of Cardiovascular Surgery 2002;31(5):359-362
Celiac artery aneurysm (CAA) is very rare. We report a case of CAA with type IIIb aortic dissection (DA) which was treated surgically. A 60-year-old man who had an abnormal enlargement of the aorta on abdominal ultrasonography was admitted to our hospital. Angiography and CT scan revealed CAA with type IIIb DA. His general condition was stable and surgery was performed electively. The CAA was exposed through a median laparotomy. It was found to be about 3cm in diameter. As vascular reconstruction seemed difficult and the proper hepatic artery showed good pulsation after clamping the common hepatic artery, we decided to perform celiac artery aneurysmectomy without vascular reconstruction. Except for transient liver dysfunction, there was no other complication and he was discharged on the 24th postoperative day. During surgery for CAA, when collateral perfusion from the SMA to the liver is adequate, it seems that vascular reconstruction is not always necessary as shown by this case.