Objective To estimate the clinical and pathological features of pancreatic solid cystic papillary tumor （SCPT） in children. Methods From 2000 to 2005

8 cases with SCPT of the pancreas were analyzed retrospectively. All cases but one were females. Average age was 12.8 years. By case review

we discussed the clinical and pathological features of SCPT in children. Results The chief complains were abdominal pain and palpable mass. There were 3 cases in the head

1 case in the body

and 4 cases in the tail of pancreas. The procedures employed included local resection （1 case）

distal pancreatectomy （5 cases）

pancreaticoduodenectomy （1 case）

and biopsy （1 case）. Histological examination showed solid with cystic areas and papillary protrusions in the 8 cases; as for immunohistochemical examinations

the positive rate was 100% for α-antitrypsin （AACT）

87.5% for vinmentin

and 62.5% for neuron-specific enolase （NSE）. The patients were followed up for 2 months to 4 years but one was lost by follow-up and all were alive postoperatively. SCPT in 2 cases relapsed. Conclusion Occurring predominantly in young females

SCPT is usually curable by surgical resection with a favorable prognosis.