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1.
J Pediatr Surg ; 40(10): e11-3, 2005 Oct.
Article in English | MEDLINE | ID: mdl-16226967

ABSTRACT

Gross E-type congenital esophageal atresia associated with congenital esophageal stenosis is extremely rare. In a male infant born at 36 weeks of gestation, bubbly vomiting was noted after birth. X-ray films of the chest and abdomen showed coil-up sign of the nasogastric tube and gas in the stomach and small intestines were recognized, so gross C-type esophageal atresia was suspected and surgery was performed on the first day of life. Surgery revealed the presence of a tracheoesophageal fistula in the upper esophagus and membranous stenosis on the distal side.


Subject(s)
Esophageal Stenosis/etiology , Esophagus/abnormalities , Tracheoesophageal Fistula/complications , Esophageal Stenosis/surgery , Humans , Infant, Newborn , Male , Tracheoesophageal Fistula/surgery
2.
Surg Today ; 35(9): 792-5, 2005.
Article in English | MEDLINE | ID: mdl-16133679

ABSTRACT

A 14-year-old boy was brought to our hospital with abdominal pain and nausea after suffering a blow to the abdomen. A mass was felt in the right hypogastrium, and the patient was hospitalized for possible hematoma resulting from the abdominal trauma. Initially, we treated him conservatively and observed his course, but on the 20th day after trauma, enhanced computed tomography showed that the area of strong enhancement in the tumor was unchanged. Superior mesenteric angiography showed findings indicative of a pseudoaneurysm caused by the trauma, and surgery was performed 26 days after the injury. Laparotomy revealed a tumor with a clear boundary, thought to originate in the mesoappendix, without any sign of pseudoaneurysm. Histopathological examination confirmed that the tumor was an omental-mesenteric myxoid hamartoma. The patient had an uneventful postoperative course and was discharged from hospital on the 12th day after surgery. More than 5 years have elapsed since the operation and no sign of recurrence or metastasis has been recognized.


Subject(s)
Hamartoma/surgery , Myxoma/surgery , Peritoneal Diseases/surgery , Adolescent , Aneurysm, False/diagnosis , Angiography , Diagnosis, Differential , Hamartoma/diagnosis , Humans , Male , Mesentery/pathology , Myxoma/diagnosis , Omentum/pathology , Peritoneal Diseases/diagnosis , Tomography, X-Ray Computed
3.
J Pediatr Surg ; 40(2): E7-8, 2005 Feb.
Article in English | MEDLINE | ID: mdl-15750916

ABSTRACT

Traumatic rupture of choledochal cyst is an extremely rare disorder. The current patient is a 4-year-old boy who fell in a bathroom and suffered a blow to the abdomen. Percutaneous transhepatic cholangiography revealed pancreaticobiliary maljunction. Inflammation of the peritoneal cavity was moderate. At first look, the choledochal cyst was excised and hepaticojejunostomy was performed. At this time, a rupture approximately 2 mm in diameter was recognized at the rear surface of the inferior part of the common bile duct.


Subject(s)
Abdominal Injuries/complications , Bile Ducts, Intrahepatic/surgery , Choledochal Cyst/complications , Choledochal Cyst/surgery , Peritonitis/surgery , Portoenterostomy, Hepatic , Abdominal Injuries/surgery , Accidental Falls , Child, Preschool , Cholangiography , Common Bile Duct/abnormalities , Common Bile Duct/surgery , Humans , Jejunostomy , Laparoscopy , Male , Peritonitis/etiology , Rupture/etiology , Rupture/surgery
4.
Pediatr Surg Int ; 21(1): 64-7, 2005 Jan.
Article in English | MEDLINE | ID: mdl-15449080

ABSTRACT

The most popular techniques for repairing large diaphragmatic defects involve the use of synthetic patches. We present an alternative approach using living tissue. We reviewed our cases of congenital diaphragmatic hernia (CDH) diagnosed within the first 24 h of life from 1991 to 2003. Toldt's fascia (TF) flap was used to repair defects that were too large to repair primarily even though the anterior rim of the diaphragm was present. After confirming that a small medial muscle remnant of the diaphragm was present, its mesothelial covering was incised, and the incision was extended to the TF far enough to create a flap sufficiently large to repair the defect. The TF flap, consisting of the small medial muscle remnant, TF, peritoneum, and retroperitoneal connective tissue, was mobilized carefully from the ipsilateral kidney and adrenal gland, and the repair completed with interrupted sutures using nonabsorbable material. We used this TF flap approach in seven of 43 patients with CDH. Two had right-sided CDH. Six survived. The mean size of the diaphragmatic defects in the seven TF flap cases was 5.43+/-0.53 x 3.86+/-1.07 cm, which was significantly larger than the defects in direct primary repair cases (3.40+/-0.77 x 2.03+/-0.59 cm) (p<0.01). The six survivors had good outcomes, and none of them have had recurrence of herniation or required any additional surgical intervention (mean follow-up period: 4.7 years). To the best of our knowledge, this is the first report of TF being used to repair large diaphragmatic hernias. Our technique is simple and has proven to be reliable for durable restoration of the diaphragm, suggesting that it could reduce the dependence on synthetic patch repair, which is associated with certain long-term complications.


Subject(s)
Fasciotomy , Hernia, Diaphragmatic/surgery , Laparotomy/methods , Surgical Flaps , Abdominal Muscles , Child , Child, Preschool , Female , Follow-Up Studies , Hernia, Diaphragmatic/diagnostic imaging , Hernias, Diaphragmatic, Congenital , Humans , Infant , Infant, Newborn , Male , Peritoneum , Radiography, Thoracic , Retrospective Studies , Treatment Outcome
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