Aneurysms of the left atrium or its appendage are uncommon. Some occur with an intact pericardium and others are associated with a pericardial defect. The majority of patients are asymptomatic, but dysrhythmias and systemic embolism may occur. The condition should be suspected after chest radiography but can only be confirmed by angiocardiography. Resection is advised with cardiopulmonary bypass standing by. A patient with an intrapericardial aneurysm of the appendage correctly diagnosed by angiocardiography and successfully treated by simple excision is described.
Gestational diabetes mellitus (GDM) is glucose intolerance first detected during pregnancy. Twin pregnancies have a higher risk of GDM, likely due to increased placental mass and elevated placental lactogen levels.
In this case report, a woman with no risk factors was admitted with bilateral tubal ectopic pregnancy. Bilateral ectopic pregnancy is a rare clinical condition with clinical findings which in their symptoms do not differ from those of unilateral ectopic pregnancy. The condition can therefore easily be missed. The risk of rupture and haemorrhagic shock might be increased because of the increased danger of both tubes presenting with complications. Thus, it is important to examine both adnexa by transvaginal ultrasound. Even if unilateral ectopic pregnancy is considered before operation, the inspection of the abdomen, especially of the other fallopian tube, must always be done during surgery.
Behçet's syndrome, a multisystem disorder, is characterized by recurrent oral and genital aphthous ulcerations, eye lesions, and skin changes. Other manifestations, although rare, may affect the nervous, gastrointestinal, or loco- motor system, as well as veins and arteries. Vascular lesions occur in approxi mately 30% of reported cases. Although thrombosis in the larger veins is frequent, arterial thrombosis is somewhat less likely to occur. Only a few cases of arterial aneurysm have been documented in the literature. This report describes a patient who had suffered from Behçet's syndrome for fifteen years and in whom a complete obstruction of the inferior vena cava was demonstrated. An aortailiac bypass was performed successfully, and the patient had had a good clinical recovery at long-term follow-up.
