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1.
Tunisie Medicale [La]. 2014; 92 (4): 275-277
in English | IMEMR | ID: emr-156271

ABSTRACT

Wandering spleen is a rare entity in child. It is generated by laxity or failure of development of spleen ligaments causing the migration of the spleen from its normal anatomical site to another abdominal or pelvic location. It can be congenital or acquired. The most dangerous complication is the occurrence of torsion of the spleen around its pedicle. Report of a new observation and present the diagnostic, treatment and outcome aspects of torsion of ectopic spleen. We report the case of a 17 years old girl who was admitted for an acute abdomen pain and fever. Clinical examination revealed generalized abdominal defence and an under umbilical mass which was very painful on palpation. Ultrasound and CT scans have visualized the pelvic mass, which measured four inches long axis. The spleen wasn't on its normal seat. The patient was operated urgently. Surgical exploration showed that the mass corresponded to a wandering spleen in pelvic position, necrotic and twisted around its pedicle. A splenectomy was performed with simple sequences. Torsion of the wandering spleen can progress to total necrosis of the spleen mass. This complication is feared in any ectopic and painful spleen

2.
Tunisie Medicale [La]. 2011; 89 (2): 195-197
in French | IMEMR | ID: emr-146501

ABSTRACT

Duodenum duplications are uncommon congenital anomalies. Most symptomatic cases are diagnosed in childhood and usually present with obstructive or bleeding symptoms. Acute pancreatitis is rarely attributed to these cysts. To report a new case of duodenum duplication revealed by acute pancreatitis. This 3 year old child presented with an acute pancreatitis. Abdominal ultrasonography and Computer tomography were performed showing a cystic mass depending of the 2[nd] duodenum. Diagnosis of duodenal duplication is made in laparotomy. A surgical resection of the duplication was performed respecting the papilla. Microscopic examination of the specimen confirmed the duodenal duplication. The patient was asymptomatic after the intervention. Duodenum duplications are uncommon congenital anomalies. Acute pancreatitis might be revealing presentation


Subject(s)
Humans , Male , Pancreatitis , Acute Disease , Tomography, X-Ray Computed , Abdomen/diagnostic imaging , Laparotomy
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