ABSTRACT
Background: Choledochal cyst is a congenital anomaly of the ducts of the extarhepaticbiliary tree. This condition is considered rare in the view of western population with an incidence of 1 in 100,000 to 150,000 births, while it defers in the Asian population where in the incidence is nearly 1 in 1000 live births. Aim: To compare and assess the advantages and disadvantages between the two standard procedures in the surgical management of choledochal cyst in children. Materials and methods: The required sample size was collected prospectively over a period of two years from November 2014 to October 2016. The decision for biliary-enteric anastomosis (Hepaticoduodenostomy Vs. Hepatico- jejunostomy) made was not influenced or directed by the study. The type of anastomosis was left to the surgeon’s personal preference in each case.15 cases of each type of biliary-enteric anastomosis – Hepatico-duodenostomy and Hepatico-jejunostomy were chosen. Results: The age distribution in cases undergoing hepatico-duodenostomy was almost near to equal, female to male ratio was of 1.25: 1. Out of 15 patients 5 in hepatico-duodenostomy group and 3 in hepatico-jejunostomy had a palpable mass in the right upper quadrant. This means that a palpable mass was seen in 26% of our patients who present for surgical correction of a CC. Second most important presenting complaint in CC was pain. Thirteen out of 30 children presented with bilious vomiting. On an average, we had initiation of feeds in the hepatico-duodenostomy group was of 5 K.V. Sathyanarayana, Sri Aparna Mummaneni. Comparative study of Hepatico-duodenostomy Vs. Hepatico-jejunostomy surgical procedures in the management of choledochal cyst in children. IAIM, 2018; 5(10): 127-137. Page 128 days and that of the hepatico-jejunostomy group was of 7 days. Average stay for the hepaticoduodenostomy group was around 7.6 days when compared to 10.5 days in the hepatico-jejunostomy group. One case in hepatico-jejunostomy group was seen to have bile leak on the 4 the post-operative day. No other early complications were seen in the hepatico-duodenostomy group. One child belonging to hepatio-duodenostomy group had been admitted three months post-operatively with the complaint of recurrent pain abdomen and fever. In cases of hepatico-duodenostomy, none of them presented with any symptoms of pain abdomen or recurrent vomiting. Conclusion: Our results also support HD as the preferred procedure for biliary reconstruction after resection of CC, in view of the advantages of relative simplicity, and low rate of complications.
ABSTRACT
Bony schwannoma is a rare benign tumour derived from Schwann cells of nerve fibres in the bone. It accounts for less than 1% of bony benign tumour, and prone to occur in the sacrum and mandible, occurrence in scapula is very rare. Here we report a 50-year-old woman with the chief complaint of pain in the left scapula. Imaging examination showed a giant, irregular, swelling lesion with distinct border involving the left scapula, extending into the left shoulder glenoid and pressing the surrounding soft tissues. Needle biopsy showed that the tumour was composed of spindle cells with S-100 protein positive, mimicking a benign neurogenic tumour. Then a complete excision was performed by removing the tumour and the surrounding tissues including partial left shoulder glenoid. Histologically, Antoni type A areas were the predominant microscopic pattern with occasional alternation by Antoni type B areas. Immunohistochemistry found that the neoplastic cells were scatteredly positive for S-100 protein. All these features suggest a diagnosis of an intraosseousschwannoma of the left scapula. Follow-up of the patient for ten months found no recurrence or sign of other tumours following complete tumour resection without any adjuvant therapy. In conclusion, this case of giant intraosseousschwannoma of the scapula is a rare benign bony tumour, and its diagnosis combined with clinical, imaging and pre-operative needle biopsy is important to guide further therapy, and avoid overtreatment.