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The aim of this study is to evaluate the efficiency of transurethral incision of ureteroceles and incidence of vesicoureteral reflux in pediatric patients with duplex system ureterocele.
This is a retrospective study of pediatric patients with duplex system ureterocele. The age of patients at the time of surgery ranged from 5 days to 17 years median — 8.
Intravesical ureterocele had patients Complications occurred in 2 patients 1. Ipsilateral vesicoureteral reflux after surgery had patients In the long-term period after transurethral incision of ureteroceles 97 patients Statistically significant risk factors associated with the need for reoperation were the presence of vesicoureteral reflux on the ureteroceles side and non-functioning upper pole of the kidney.
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Even more rarely, duplication cysts are not anatomically connected to the stomach and are located in other parts of the abdominal cavity or in the retroperitoneal space.
Cystic duplication of the gastrointestinal tract, which are localized in the pancreas, is extremely rare. The aim of the study is to demonstrate the possibility of using laparoscopy for this disease.
The paper describes three rare clinical observations of gastric duplication cyst topographically associated with the pancreas. In the first clinical observation, gastric duplication cyst was combined with mediastinal duplication cysts, an esophageal bronchial fistula, and extralobar pulmonary sequestrations.
In the second observation, a duplication cyst had communication with the pancreatic duct system and was clinically manifested by recurrent bleeding.
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Histological examination in all the described observations confirmed the gastric type of epithelium of the mucous membrane of the cysts.
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The described rare clinical manifestations, a combination of defects, as well as the possible presence of heterotopy of the mucous membrane of the duplication cyst confirm the need for surgical correction of the disease.
When revealing a sacrococcygeal tumor in pediatric patient especially — newborn , a germ-cell tumor GCT mostly — teratoma should be suspected.
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We analyzed the data of charts of patients with sacrococcygeal GCT from 2 clinics of St. Petersburg pediatric surgical hospital CCMCSCHMT and pediatric oncological department of St.
Petersburg Oncocenter for past 15 years — In both cases of small-sized GCT prenatal ultrasound was unable to reveal the tumor.
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