The most common mandibular fractures involve the condyloid process. It is necessary to diagnose and treat the cases of mandibular condylar fracture carefully, because the temporomandibular joint is complicated anatomically and functionally.
A clinical study was made in 72 patients with mandibular condylar fracture referred to the Department of Oral and Maxillofacial Surgery, Gunma University Hospital from April 1991 to March 1995.
The results were as follows:
1. Mandibular condylar fracture occurred in 42.6% of the mandibular fractures. The male-to-female ratio was 2 to 1. The largest age group of patients was from 10 to 19 years (31.9%).
2. The most frequent cause of the injury was falls (50.0%). Of all the patients 84.7% visited our department within 2 weeks after injury.
3. Fifty-nine cases (81.9%) were unilateral fractures and 13 (18.1%) were bilateral. Of the total, thirty-six cases (50.0%) were combined with other fractures of the mandible and/or maxillofacial fractures.
4. As for the fracture level and position of fragment, fractures with deviation were most frequently observed in the subcondylar region (20.5%).
5. Of the 67 cases treated at our department, 62 (92.5%) were treated with a conservative therapy for mandibular condylar fracture, primarily by maxillomandibular fixation followed by functional rehabilitation. The remaining 5 (7.5%) cases were treated surgically.
6. Fifty-nine patients were recalled after more than 6 months. As for the treatment outcome in 54 nonsurgical cases, 46 cases (85.2%) showed excellent prognosis, 6 (11.1%) had disorder I and 2 (3.7%) had disorder II. In 5 surgical cases, 3 cases showed excellent prognosis and 2 had disorder II. Most of the patients treated nonsurgically had relatively good results.

A case of mycotic aneurysm in the gastroduodenal artery associated with infectious endocarditis (IE) penetrating into the residual stomach is reported. A 50-year-old woman was transferred to our hospital because of sudden onset of hematemesis and bloody stool. She had had partial gastrectomy due to duodenal ulcer 6 years previously and aortic prosthetic valve replacement due to infectious endocarditis eight months previously. Emergency laparotomy was performed. Aneurysm of the gastroduodenal artery penetraing into the lumen of the residual stomach was found. The aneurysm had not been detected in the CT scan 8 months earlier. It was surmised that it was related to IE and had developed over the last 8 months. Aneurysmectomy was performed. The postoperative course was uneventful and she was discharged on the 22nd postoperative day. Mycotic aneurysm associated with IE developing into the gastroduodenal artery and penetrating into the stomach is rare. It is possible that a mycotic aneurysm could develop in any artery of a patient with IE. We should thus carefully examine patients with IE in order to detect mycotic aneurysms using angiography and the contrast-enhanced CT scan.

Dacron grafts have made great progress and the material has become almost perfect recently. However, we encountered a rare case of a late-graft complication. A 34-year-old man was operated on for coarctation of the aorta in July 1982. Left subclavian artery-descending aortic bypass was performed using a Cooley double velour knitted graft. Eighteen years later, the patient was admitted to our hospital with an abnormal shadow in his chest X-ray. Angiography and computed tomography demonstrated a non-anastomotic aneurysm of the graft. Under cardiopulmonary bypass and deep hypothermic circulatory arrest, reoperation with a woven Dacron graft was successfully performed. This case suggests that it is important to follow up patients with implanted Dacron arterial prostheses because of the potential for rupture.

Gelatin-resorcin-formalin (GRF) glue has been widely used in repair of dissected aortic wall tissue, and the use of GRF glue has been reported to significantly reduce mortality from this surgical emergency. On the other hand, various late complications possibly due to GRF glue have also been reported. We performed reoperations after total arch replacement for acute type A aortic dissection using GRF glue in 2 cases. In case 1, total arch replacement was performed 3 years ago. Pseudoaneurysms of the aortic root and brachiocephalic artery and redissection of the descending aorta were revealed by subsequent computed tomography (CT). Partial graft replacement for these 3 sites were performed with open distal anastomosis and right common carotid artery perfusion. In case 2, total arch replacement was performed 5 years previously. Redissection of the aortic root was revealed by CT, and ultrasound cardiography revealed severe aortic regurgitation and severe mitral valve insufficiency. A modified Bentall procedure and mitral valve replacement were performed. In these 2 cases, the sites of redissection and pseudoaneurysm were identified as the sites of use of GRF glue at the first operation. We suspected that the use of GRF glue is associated with a certain amount of risk of redissection and pseudoaneurysm. Such patients should be carefully followed for years after surgery. It is necessary to use appropriate surgical and glue application techniques to obtain the desired effect of the glue.

A 75-year-old man, who had undergone aortic valve and ascending aorta replacement at the age of 73 years, was admitted to our hospital with one week of fever. Blood culture showed growth of Streptococcus bovis and echocardiography showed vegetation on the prosthetic valve. Although antibiotic treatment was commenced, he complained of abdominal pain, and computed tomography showed a superior mesenteric artery embolism. The abdominal pain improved with fasting, but echocardiography showed another vegetation, and re-aortic valve replacement was performed to prevent embolism recurrence. When he resumed eating postoperatively, he again complained of abdominal pain and computed tomography showed mesenteric ischemia. The necrotic intestine was extensively resected and he recovered successfully. A superior mesenteric artery should be revascularized to 2/11 prevent perioperative mesenteric ischemia when cardiac surgery complicated by acute superior mesenteric artery embolism is performed.

We describe a case of cardiac surgery for a patient with CD36 deficiency. A 56-year old man had progressive dyspnea on effort for 1 year. On admission, echocardiography revealed severe aortic valve regurgitation. He required medical treatment for heart failure, and subsequently elective aortic valve replacement was planned. Pre-operative cardiac scintigraphy (¹²³I-BMIPP) showed total defect of myocardial uptake. CD 36 deficiency was diagnosed based on the characteristic findings. CD 36 deficiency could cause transfusion related complication by donor blood transfusion. We prepared 1,200 ml autologous blood preoperatively in a two week period. The operation was performed successfully without donor blood transfusion. He was discharged uneventfully.

We report a case of surgical treatment for pseudoaneurysm 19 years after aortic root replacement. The patient was a 57-year-old female who had undergone aortic root replacement (Piehler procedure) in another hospital due to acute Stanford A type aortic dissection in 1988, and was then followed up at another hospital. However, a low density area around the artificial graft was pointed out on computed tomography (CT) in 2001, which increased to 60mm in size by November, 2006. She was then referred to our hospital for a redo operation. Pseudoaneurysm of the anastomosis and mitral regurgitation (MR) was diagnosed by the examination of the CT, angiography, etc., and we performed ascending aorta and aortic arch replacement, and mitral valve replacement (MVR) in April, 2007. A slight hemorrhage were found at the anastomosis of the artificial graft-artificial graft. Deterioration of the artificial graft or deterioration of the suture was suspected as the cause of the slight hemorrhage from the anastomosis a long period after the operation. In this case, loosening of the suture string was revealed, so the latter was more strongly suspected.

A 56-year-old man was admitted to our institution with sudden onset of severe chest pain and ischemia of the lower extremities on February 24, 2007. An enhanced computed tomography scan showed acute Stanford type A aortic dissection. Electrocardiography showed ST segment elevation in leads V_1-4 and a transthoracic echocardiogram revealed antero-septal wall akinesis. The patient was given a diagnosis of acute myocardial infarction (AMI) caused by left main trunk dissection (LMT) due to acute aortic dissection. Coronary angiography (CAG) showed severe stenosis in the LMT with poor distal run-off. For this reason, after we implanted a stent in the left main coronary trunk to maintain coronary blood flow, we performed total aortic arch replacement, coronary artery bypass grafting (SVG-LAD #8), and F-F cross-over bypass. Removal of the implanted stent from the LMT during the operation was simple. Postoperative CAG showed a patent SVG and intact LMT. Because preoperative PCI is still controversial for acute aortic dissection with AMI, either more immediate surgery or preoperative PCI (bridge stent to surgery) in the left main coronary artery is mandatory. Implantation of an LMT stent, as a bridge to surgery, is an effective strategy for acute type A aortic dissection with LMT occlusion before surgical repair.

We report a case of successful surgical treatment for acute aortic dissection in a patient with late pregnancy with Marfan syndrome. The patient was a 32-year-old primipara. She experienced sudden precordial pain and visited on other hospital at 29 weeks' gestation. She was given a diagnosis of acute type A aortic dissection on computed tomography (CT), and was referred to our hospital for surgery. The earliest possible operation was required, but, in view of the risk of massive bleeding following placental separation due to heparin administration for cardiopulmonary bypass, Caesarian section and abdominal total hysterectomy were initially performed, followed 2 days later by the Bentall procedure plus prosthetic graft replacement of the ascending aorta and aortic arch in a two-stage operation. The postoperative course of the mother and infant was uneventful. The treatment strategy for Marfan syndrome complicated by aortic dissection in late pregnancy is very important. We were able to safely perform surgery and perioperative management using a two-stage operation, that is, by performing Caesarian section first, then strictly controlling circulatory dynamics under sedation and artificial ventilation in the ICU, and subsequently performing repair of the heart and aorta after the subsidence of obstetric hemorrhage.

A semicomatose 53-year-old woman who had been injured in an automobile accident was admitted. Injury to the thoracic descending aorta was suspected because of widening of the upper mediastinum on a chest X-ray film and confirmed by chest contrast-enhanced computed tomography (CT). We postponed surgical treatment because brain CT showed traumatic intracerebral hemorrhage. She was maintained in an intensive care unit and had pharmacological treatment and medical support. Two days later, brain CT showed that the intracerebral hematoma was a stable and inactive lesion, so she underwent aortic repair 3 days after the accident. Left thoracotomy was performed and an artificial vascular prosthesis was interposed under hypothermic circulatory arrest (open proximal method). The postoperative course was uneventful and the patient was discharged 44 days after the operation. Hypothermic circulatory arrest may be a valuable adjunct for traumatic injury of the thoracic aorta at risk for impending rupture.