ABSTRACT
Imperforate hymen is a relatively rare congenital anomaly. However, it is not an uncommon cause of lower abdominal pain presenting in teenage girls. Without careful history taking and thorough examination, the condition can be missed easily. We report an imperforate hymen presenting as abdominal pain in three teenage girls aged 12, 12 and 13 years, respectively, within a six-month period. The presentation was reviewed and the various types of hymenotomy were discussed.
Subject(s)
Abdominal Pain/etiology , Hematocolpos/diagnosis , Hymen/abnormalities , Hymen/surgery , Abdominal Pain/surgery , Adolescent , Amenorrhea/etiology , Amenorrhea/surgery , Child , Female , Hematocolpos/surgery , Humans , Urinary Retention/etiology , Urinary Retention/surgeryABSTRACT
PURPOSE: To assess the intermediate-term result of the use of the minimally invasive technique in the treatment of choledochal cysts in children. METHODS: This is a retrospective review of all cases of choledochal cyst treated in the tertiary referral centre. The surgical technique is described and all the medical records were reviewed to assess the intraoperative and postoperative complications and follow-up problems. RESULTS: From October 2000 to April 2008, laparoscopic excision and reconstruction were attempted in 37 patients. Laparoscopic surgery was successfully performed in 34. Conversion was required in three patients due to oozing on cyst dissection (two) and bleeding from small bowel mesentry (one) during the early part of the series. Postoperative complications were observed in 15 patients including subhepatic collection (6), bile leakage (3), minor wound infection (4) and prolonged ileus (2). At a mean follow-up of 4.2 years, four patients developed surgical complications including intrahepatic ductal strictures in a type IV cyst (one), stump pancreatitis (one), terminal ileal obstruction from internal herniation (one) and cholangitis (one). The cosmetic result was good in all patients. CONCLUSION: We conclude that laparoscopic excision and reconstruction can be safely performed in children with a choledochal cyst with satisfactory intermediate-term results.
Subject(s)
Choledochal Cyst/surgery , Laparoscopy/methods , Adolescent , Anastomosis, Surgical/methods , Child , Child, Preschool , Choledochal Cyst/diagnosis , Female , Follow-Up Studies , Hepatic Duct, Common/surgery , Humans , Infant , Infant, Newborn , Jejunostomy/methods , Male , Time Factors , Treatment OutcomeABSTRACT
Neuroblastoma is the most common extracranial solid tumor in children. Primary omental neuroblastoma has never been reported in the English literature. A 4-year-old girl presented with a mobile abdominal mass; primary omental neuroblastoma was diagnosed. There was tumor recurrence after complete tumor resection. She received chemotherapy and underwent laparoscopic resection of the recurrent tumor. There was no tumor recurrence after 1 year of follow-up.
Subject(s)
Neoplasm Recurrence, Local/surgery , Neuroblastoma/surgery , Omentum , Peritoneal Neoplasms/surgery , Child, Preschool , Female , Humans , Laparoscopy , Neoplasm Recurrence, Local/drug therapy , Neuroblastoma/diagnosis , Peritoneal Neoplasms/diagnosisABSTRACT
Littre's hernia is a rare complication of Meckel's diverticulum. It was originally defined as 'the presence of a Meckel's diverticulum in any hernia sac' by Rieke in 1841. It is difficult to diagnose before surgery. With the advances in the development of laparoscopic surgery in children, diagnosis of this rare condition, together with subsequent repair of Littre's hernia and Meckel's diverticulectomy can be performed by laparoscopy. We herein report the use of laparoscopy in the management of two boys with Littre's hernia, including one with incarcerated hernia.
Subject(s)
Hernia, Inguinal/surgery , Laparoscopy/methods , Plastic Surgery Procedures/methods , Child, Preschool , Diagnosis, Differential , Follow-Up Studies , Hernia, Inguinal/diagnosis , Hernia, Inguinal/etiology , Humans , Infant , Male , Meckel Diverticulum/complications , Meckel Diverticulum/diagnosisABSTRACT
BACKGROUND: Meckel's diverticulum, the most common congenital anomaly of the gastrointestinal tract, is prone to develop complications in the pediatric population. The authors report their 10-year experience with the management of complicated Meckel's diverticulum in children using laparoscopy. METHODS: A retrospective review of all complicated Meckel's diverticulum cases involving children from 1998 to 2007 was performed. The efficacy and safety of laparoscopy used to manage complicated Meckel's diverticulum were assessed. RESULTS: Over a 10-year period, 20 children (17 boys and 3 girls) with a mean age of 5 years (range, 7 months to 13 years) were included in the study. Of the 20 children, 12 presented with gastrointestinal bleeding, 2 had intestinal obstruction, 3 had abdominal pain mimicking acute appendicitis, 2 had inguinal hernia, and 1 had intussusception. Diagnostic laparoscopy was performed for all the patients. Laparoscopically assisted transumbilical Meckel's diverticulectomy was performed successfully for 18 of the children. The operative time ranged from 50 to 190 min (mean, 115 min). All the children had an uneventful recovery except one, who experienced a postoperative wound infection. Ectopic gastric mucosa was found in 14 cases. CONCLUSIONS: Diverse pediatric surgical conditions result from Meckel's diverticulum. Laparoscopy is a safe and effective method for the management of complicated Meckel's diverticulum.
Subject(s)
Gastrointestinal Hemorrhage/etiology , Intestinal Obstruction/etiology , Laparoscopy/methods , Meckel Diverticulum/surgery , Adolescent , Child , Child, Preschool , Female , Follow-Up Studies , Gastrointestinal Hemorrhage/surgery , Humans , Infant , Intestinal Obstruction/surgery , Male , Meckel Diverticulum/complications , Retrospective Studies , Treatment OutcomeABSTRACT
We report a case of pheochromocytoma in the urinary bladder of a 14-year-old girl who presented with headache and palpitation after voiding. This is an extremely rare condition in pediatric age group and thus can be missed easily. This case is the seventh case reported in the reviewed literature.
