the present report describes a male newborn with a pulsatile structure beneath the sternum. echocardiography showed common atrium, a single ventricle, mitral atresia, double outlet right ventricle, subpulmonary stenosis, small pulmonary artery branches, and a thin walled ventricular diverticulum suggestive of cantrell's syndrome. the diverticulum was resected to prevent life threatening events ...

Meckel's diverticulum is the most common congenital abnormality of the gastrointestinal tract. In the vast majority of cases it remains asymptomatic throughout life but in about 5% of cases it gives rise to complications, namely, haemorrhage, intestinal obstruction and inflammation. A rare complication is being presented--a femoral hernia containing a strangulated Meckel's diverticulum. This is...

Present work was directed to study the prevalence and anatomical basis of diverticulum formation and its association with malignancy inside the urinary bladder on cadavers. Urinary bladder diverticulum and its complications including malignancy has been reported by different authors based on their study on radiological findings and endoscopy. Present study was undertaken on cadavers to meet the...

Diverticulum of the abdominal esophagus is an extremely rare disease. We present a patient with diverticulum of the abdominal esophagus who could be treated successfully by a laparoscopic diverticulectomy with supporting intra-operative endoscopy. In patient with epiphrenic diverticulum, diverticulectomy with myotomy and partial fundoplication is recommended as surgical treatment. This procedur...

We describe the case of a 31-year-old man who had a giant right atrial diverticulum. Although he was asymptomatic, preoperative echocardiography and three-dimensional computed tomography scan found a large mass on the right atrium. He was diagnosed with a right atrial diverticulum and underwent surgical resection of the diverticulum because of the risk of thromboembolism, arrhythmia and rupture...

We herein report a case of Killian-Jamieson diverticulum mimicking a thyroid tumor. Killian-Jamieson diverticulum is a rare form of hypopharyngeal pulsion diverticulum resulting from herniation of mucosa and submucosa through an area of weakened musculture [1]. The diverticulum is caudal to that of the more common Zenker’s diverticulum [2]. These hypopharyngeal diverticula that cause dysphagia ...

BACKGROUND Meckel's diverticulum is a congenital anomaly of the gastrointestinal tract. About 98% of affected patients are asymptomatic. Small intestinal examination has become easier since the development of double-balloon enteroscopy. The present case series describes 10 patients with Meckel's diverticulum in whom double-balloon enteroscopy was useful for diagnosis. CASE PRESENTATION Ten pa...

The presence of a Meckel's diverticulum in the hernial sac is called Littre's hernia. It rare complication diverticulum. We present 56-year-old male patient who complained swelling umbilical region. After clinical examination and imaging studies, we diagnosed with partially reducible underwent exploration was found to have omentum, diverticulum, part ileum within sac. segmental resection bowel,...