Echinococcus is endemic in some parts of the world but cardiac involvement with hydatid cyst is rare. Here, we report a 55-year-old man who developed right ulnar fracture and was scheduled for surgery. During routine preoperative evaluation abnormal findings in ECG were found. In echocardiography, a large mass was detected in the inferior wall of the left ventricle. Coronary angiography showed ...

background kawasaki disease (kd) is an acute multisystem vascular syndrome of unknown etiology that is the leading cause of acquired heart disease in children of developed counties. objectives we aimed to evaluate the epidemiological characteristics and clinical manifestations of kd in children residing in the southwest of iran. patients and methods in this retrospective study, we reviewed the ...

hydatid disease commonly involves liver but in rare cases, it can involve cardiac structures. a 75-yr-old farmer from parsabad-moghan, northwestern iran was presented to the emergency room of tehran imam khomeini hospital, tehran, iran with dyspnea and without chest pain in 2014. a lesion compatible with hydatid cyst was found in echocardiography and confirmed by serology and mri. surgical trea...

Holt-Oram syndrome is an autosomal dominant disorder, characterised by skeletal abnormalities of the upper limb associated with congenital heart defect, mainly atrial and ventricular septal defects. Skeletal defects exclusively affect the upper limbs in the preaxial radial ray distribution and are bilateral and asymmetrical. They range from clinodactyly, absent or digitalised thumb, hypoplastic...

introduction the pericardial agenesis is a rare congenital anomaly. classified as partial or total being asymptomatic in most cases, but some patients are at risk for serious complications and death, and these have indication for surgical treatment. case presentation this paper describes the case of a 21 year old patient, with atypical precordial pain, diagnosed with agenesis of the left perica...

A 22 year old male referred with palpitation. General appearance and physical exam impressed us in that the patient has Marfan syndrome. Cardiac catheterization showed diffuse arterial ectasia. We found no previous report of this generalized diffuse ectasia.