Splenectomy for wandering splenomegaly in a patient with idiopathic thrombocytopenic purpura: A case report of a rare association.

• The absence or malformations of splenic suspensory ligaments attaching the spleen to the diaphragm, colon, and retroperitoneum is the major cause of wandering spleen (WS). • Diagnosis is often an occasional finding during radiological exams. • Conservative treatment may lead to high complications.

Adult's congenital bile duct cysts.

Introduction: Congenital bile duct cysts (CBDC) is a rare congenital malformation. It results from an anomaly of the biliopancreatic junction (AJBP). This condition is often diagnosed at a young age.

[Epidemiological, clinical features, therapeutic results and evolution of gastrointestinal stromal tumour: about 25 cases].

Background: Gastrointestinal stromal tumors (GIST) are mesenchymal tumors occuring in the majority of cases in the stomach and small intestine, rarely in rectum, colon, esophagus or mesentery. They are derived from cells of cajal or their precursor, and are typically CD117/KIT + (95%), CD34 + (70%).

Aims: is to study the epidemiological, clinical, therapeutic and evolution of gastrointestinal stromal tumors.

[Intussusception in adults. Thirteen case reports].

This study was retrospective. The authors analyse the clinical, etiological and therapeutic aspects of the intestinal intussusception based on 13 adults observed over 14 years in the surgical department of the university hospital in Monastir. This disease was rare because accounted for 2.