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Extrahepatic biliary cystadenomas and cystadenocarcinoma. Report of seven cases and review of the literature.

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OBJECTIVE The aim of this investigation was to describe the clinical features, diagnosis, pathologic characteristics, and optimal surgical management for patients with extrahepatic biliary cystadenomas. BACKGROUND Extrahepatic biliary cystadenomas are rare epithelial neoplasms. The clinical features

[Mucin-producing cystadenoma (borderline malignancy) of the renal pelvis and ureter. A case report].

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The patient was a 63-year-old women who visited our hospital with the chief complaints of swelling, chills, fever and right lumbago. Fifteen years ago, she received surgical exploration for right renal stones at another department of urology. A large, soft and round kidney was palpable from the

Surgical management of biliary cystadenoma and cystadenocarcinoma of the liver.

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Biliary cystadenoma (BCA) and biliary cystadenocarcinoma (BCAC) are rare biliary duct neoplasms. This study investigated reasonable management strategies of cystic neoplasms in the liver. Charts of 39 BCA/BCAC patients (9 males, 30 female; median age 53.74 ± 14.50 years) who underwent surgery from

[Pancreatic mucinous cystadenoma doubly complicated by acute pancreatitis and retroperitoneal rupture].

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Mucinous cystadenomas are benign tumors with malignant potential. They are often revealed by non-specific abdominal pain, jaundice or an episode of acute pancreatitis. We here report an exceptional case of mucinous cystadenoma doubly complicated by acute pancreatitis and retroperitoneal rupture. The

[Diagnosis and treatment of cystadenoma and cystadenocarcinoma: experience in 8 cases].

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OBJECTIVE To summarize the experience in the diagnosis and treatment of biliary cystadenoma and cystadenocarcinoma. METHODS The clinical data of 8 patients of biliary cystadenoma and cystadenocarcinoma, 3 males and 5 females, aged 55.8 (26 approximately 71), were analyzed

Clinicopathological features and post-resection outcomes of biliary cystadenoma and cystadenocarcinoma of the liver.

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OBJECTIVE Biliary cystadenoma (BCA) and biliary cystadenocarcinoma (BCAC) account for 5%-10% of liver cystic diseases. In this study, we analysed the clinical presentation and surgical management of patients with BCA and BCAC. METHODS We retrospectively analysed the medical records of 23 BCA and 7

Intraperitoneal hyperthermia in the management of pseudomyxoma peritonei.

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OBJECTIVE Pseudomyxoma peritonei is a rare disease characterized by diffuse intraperitoneal mucinous tumor and massive mucinous ascites. The mainstay of treatment is surgery in combination with adjuvant therapy. METHODS From 1995 to 2002, 8 patients with pathologically confirmed pseudomyxoma

Giant mucinous cystadenoma in a young patient. A case report.

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The Authors describe the clinical case of a seventeen-year-old girl who presented with abdominalgia, fever, nausea and vomiting. During surgery it proved necessary to remove not only the appendix but also a voluminous mucinous cystadenoma of the ovary. The authors take this observation as a starting

Arrangements of hepatobiliary cystadenoma complicated with congenital choledochal cyst: a case report and literature review.

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Hepatobiliary cystadenoma complication with congenital choledochal cyst is extremely rare and has never been reported in literatures so far.The aim of the study was to investigate the disease arrangements by analyzing the case and performing a systematic review of the literature.This case report

Laparoscopic resection of appendiceal mucinous cystadenoma.

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Mucinous cystadenoma is a rare lesion of the vermiform appendix and is seldom diagnosed before surgery, although radiologic and ultrasonographic findings have been reported. We present the case of a 65-year-old female with rheumatoid arthritis who presented with general malaise, poor appetite,

Laparoscopic Anatomical Left Hepatectomy for Intrahepatic Bile Duct Papillary Mucinous Cystadenoma With Intraoperative Vascular Repair: A Case Report.

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Laparoscopic hepatectomy has been widely performed for patients with benign liver tumors such as hepatic hemangioma, focal nodular hyperplasia, and hepatic adenoma.We here present a case of a 78-year-old female patient who was initially admitted to our department due to fever and jaundice for 2

Hepatobiliary cystadenomas and cystadenocarcinomas: a report of 33 cases.

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BACKGROUND Hepatobiliary cystadenomas and cystadenocarcinomas are rare and often misdiagnosed. OBJECTIVE We report our experience with 33 cases over 20 years to discuss an algorithm for these diseases. METHODS Patients presenting with a diagnosis of hepatobiliary cystadenomas and cystadenocarcinomas

Percutaneous aspiration of peripancreatic fluid collections: a safe method to detect infection.

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During the past 5 years, we have used percutaneous aspiration of peripancreatic fluid collections guided by computed tomography (CT) or ultrasonography (US) to facilitate diagnosis of infection in selected cases. Fifteen of 18 patients undergoing guided needle aspiration had persistent fevers

Benign enterogenous cyst of the pancreas.

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A 26-year-old woman was evaluated for a mass found by computed tomography (CT). Radiographically, the mass resembled a pancreatic cystadenoma. The patient had had left upper quadrant abdominal pain for several years and low grade fevers and indigestion for 5 months. At surgery, a unilocular cystic

Marked diffuse dilations of the biliary tree associated with intrahepatic calculi, biliary sludges and a mucinous cyst of the pancreatic head in a 99-year-old woman.

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A 99-year-old woman was admitted to Shizuoka Shimizu Municipal Hospital because of fever and anasarca. Imaging and laboratory tests showed pneumonia, urinary tract infection, and cardiac failure. The patient died 20 days after admission. An autopsy revealed marked diffuse dilations of the biliary

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