Adenosquamous carcinoma of gallbladder associated with biliopancreatic maljunction and Todani 1c choledochal cyst: A case report
نویسندگان
چکیده
Gallbladder cancer is the fifth most frequent women in Algeria. Squamous-cell and adenosquamous carcinomas are rarest histological type of this represent less than 7%. Malformation bile ducts such as a choledochal cyst or biliopancreatic maljunction risk factors for cancer. This manuscript reports rare case an 82-year-old woman operated on carcinoma gallbladder associated with duct junction abnormality. Aggressive surgery was performed combined adjuvant oral chemotherapy. Twenty-nine months recurrence-free survival achieved by patient suffering from aggressive form
منابع مشابه
Choledochal cyst Todani IA case report
BACKGROUND Choledochal cyst is a congenital dilatation of the biliary tree. It may affect only the extrahepatic bile duct (type I, II and III), intrahepatic (type V) or both (type IVa). Vater first described choledochal cyst in 1723. Open excision was the standard procedure made a great impact in the treatment but since 1995 Farello et al. first reported laparoscopic choledochal cyst excision a...
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Choledochal cyst is a relatively rare condition. Even rarer is a choledochal cyst in association with a gallbladder carcinoma. This study reports a rare case of gallbladder carcinoma coexisting with a choledochal cyst in a Nigerian patient. Clinical records of the patient including preoperative evaluation, intraoperative findings, and postoperative care were reviewed. A 38-year-old woman presen...
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Adenosquamous carcinomas of stomach are rare entities comprising 0.5% of stomach carcinomas. Here, we report a case of a 50-year-old female, who presented with weakness, pallor, and symptoms of gastric outlet obstruction. A partial gastrectomy was done and histology showed evidence of adenosquamous carcinoma of the antrum with metastasis to the perigastric lymph nodes. The patient condition ...
متن کاملCholedochal cyst. Report of a case.
Four cases of Choledochal Cyst are presented. The preoperative diagnostic difficulty is re-emphasized. The pathology and surgical management is discussed. Choledochal Cysts are uncommon but correct management ensures symptom free future for the patient. Recent report advocating cyst excision, if technically possible, is also reviewed (JPMA 37:105 1987).
متن کاملCongenital choledochal cyst. A case report.
A congenital choledochal cyst presented as an upper abdominal mass in a non-jaundiced woman; at laparotomy total cystectomy was performed and biliary enteric continuity re-established by a hepaticojejunostomy Roux-en-Y anastomosis.
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ژورنال
عنوان ژورنال: Advances in Digestive Medicine
سال: 2022
ISSN: ['2351-9797', '2351-9800']
DOI: https://doi.org/10.1002/aid2.13327