The authors present a clinical case of an extremely rare combination of the congenital defect of the front abdominal wall as omphalocele, congenital evolution defect of the small intestine - atresia of the small intestine type III, agenesis of the ileum with ileocecal angle and malrotation syndrome. Surgical treatment was as follows: T-shaped ileocolic «end-to-side» anastomosis with an unloading colostomy by the Bishop-Koop technique and intestinal intubaton till the Treitz ligament. Outcomes of such surgical correction are good.
A solid pseudopapillary tumor of the pancreas is a very rare tumor of unclear histogenesis. Its frequency is 1–2% of the total number of exocrine tumors and about 5% of cystic tumors of the pancreas. Only 130 mainly publications related to separate clinical observations of this pathology are available in medical literature. We found no works describing the complicated course of a solid pseudopapillary tumor of the pancreas in children. The article describes a clinical case with a probable complicated, life threatening course of a solid pseudopapillary pancreatic tumor in children due to peptic erosion of tissues and vessels with capsular rapture.
Retroperitoneal lipoma is extremely rare in pediatric practice. This article describes the diagnosis and treatment tactics of a clinical case of retroperitoneal lipoma in a 4- year-9-month-old child. The operative intervention is a rational method of this disease treatment.
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