No abstract available.
Peutz-Jeghers Syndrome*

No abstract available.
Anemia, Hypoplastic, Congenital*

No abstract available.
Hydronephrosis* ; Teratoma*

No abstract available.
Heterotaxy Syndrome*

No abstract available.
Tuberous Sclerosis*

No abstract available.
Abdomen, Acute* ; Nephritis* ; Purpura, Schoenlein-Henoch*

No abstract available.
Female ; Pregnancy ; Pregnancy, Ectopic*

Tubulovillous adenoma of the stomach is an intermediate between tubular and villous adenoma, and may exhibit both growth patterns. Pedunculated tubulovillous adenomas behave clinically and pathologically like tubular adenoma and sessile tubulovillious adenomas tend to behave like villous adenoma., stamach is unusual site of involvement. Tubulovillous adenoma of the stomach has a great tendency to undergo malignant change. Malignant Change are correlated with polyp size and the proportion of villous componancy. And those in the stomach are highly assoeiated with an independent gastric carcinoma. Endoscopic biopsy may confirm the diagnosis but may give false positive results for malignant neoplasm and therefore should not delay, treatment. After diagnosis, surgical resection is mandatory and subsequent radiological or endoscopic follow-up is essential. Recently We experienced a 46-year-old female patient whio had a large tubulovillous adenoma of the stomach with careinomatous change and reviewed this case with references.
Adenoma* ; Adenoma, Villous ; Biopsy ; Diagnosis ; Female ; Humans ; Middle Aged ; Polyps ; Stomach*

Choledochal cyst is a relatively rare disease entity considered to be a congenital cyatic dilatation of the common bile duct. Since occurrence of malignant tumor in choledochal cyet was first reported by Irwin and Morrison in 1944, approximately 100 more cases of malignant tumors arising in congenital choledocal cyst have been reported in the world, and the risk of malignant tumor related to choledochal cyst have been reported 2.4-14%. Recently, we experienced a case of adenocarcinoma arising in choledochal cyst in 39 year-old woman who was diagnosed by ERCP and cholangioscopy with forceps biopsy, and was treated with en bloc resection of the choledochal cyst along with the pancreatic head and duodenum.
Adenocarcinoma ; Adult ; Bile Duct Neoplasms ; Biopsy ; Cholangiocarcinoma* ; Cholangiopancreatography, Endoscopic Retrograde ; Choledochal Cyst ; Common Bile Duct ; Dilatation ; Duodenum ; Female ; Head ; Humans ; Rare Diseases ; Surgical Instruments

Choledochal cyst is a relatively rare disease entity considered to be a congenital cyatic dilatation of the common bile duct. Since occurrence of malignant tumor in choledochal cyet was first reported by Irwin and Morrison in 1944, approximately 100 more cases of malignant tumors arising in congenital choledocal cyst have been reported in the world, and the risk of malignant tumor related to choledochal cyst have been reported 2.4-14%. Recently, we experienced a case of adenocarcinoma arising in choledochal cyst in 39 year-old woman who was diagnosed by ERCP and cholangioscopy with forceps biopsy, and was treated with en bloc resection of the choledochal cyst along with the pancreatic head and duodenum.
Adenocarcinoma ; Adult ; Bile Duct Neoplasms ; Biopsy ; Cholangiocarcinoma* ; Cholangiopancreatography, Endoscopic Retrograde ; Choledochal Cyst ; Common Bile Duct ; Dilatation ; Duodenum ; Female ; Head ; Humans ; Rare Diseases ; Surgical Instruments