cystadenocarcinoma/hitasótt

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[Establishment of a new human ovarian serous cystadenocarcinoma cell line (IM), and influence on cell proliferations by cisplatin with or without hyperthermia].

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A new cell line, designated IM has been established from operation material derived from a woman with ovarian serous cystadenocarcinoma. The population doubling time of the 35th passage IM cell was 28.8 hours. And it was successively subcultured 165 times in over 7 years, moreover still kept CA125

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

Intrahepatic biliary cystadenocarcinoma: clinical analysis of 4 cases.

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BACKGROUND Intrahepatic biliary cystadenocarcinoma (IBC) is a low-incidence disease which is often misdiagnosed because of insufficient recognition. This study aimed to investigate the clinical features, diagnosis and treatment of the disease. METHODS The clinical data of 4 IBC patients treated in

Augmentative effects of intracellular chemotherapy penetration combined with hyperthermia in human ovarian cancer cells lines.

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A significant proportion of ovarian cancer patients do not achieve a complete response to chemotherapy, due mainly to the evolution of clones resistant to cytotoxic drugs. Exploring possibilities to overcome this resistance constitutes a challenge in the study of ovarian cancer experimental therapy.

[A case of mucinous cystadenocarcinoma of the appendix with abdominal wall abscess successfully treated by percutaneous drainage and systemic chemotherapy-a case report].

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A 76-year-old woman was diagnosed of mucinous cystadenocarcinoma of the appendix. Since there was wide direct invasion into the right psoas muscle, she was judged as inoperable although she had no bowel obstruction. She was received FOLFIRI and bevacizumab treatment. After the first cycle, the tumor

[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

A case of biliary cystadenocarcinoma.

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Biliary cystadenocarcinoma is a very rare cystic tumor that arises in the liver or, less frequently, in the extrahepatic biliary system. It has been shown to arise in congenital liver cysts, bile ducts, biliary cystadenoma, in the context of fibropolycystic disease and in the hepatoduodenal

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

Adenosquamous carcinoma of the liver arising in biliary cystadenocarcinoma: clinical, radiologic, and pathologic features with review of the literature.

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Primary biliary cystadenoma, cystadenocarcinoma, squamous carcinoma, and adenosquamous carcinoma of the liver are rare tumors. We describe a middle-aged woman with recurrent fever and a clinical diagnosis of hepatic abscess who proved at laparotomy to have adenosquamous carcinoma of the liver

Huge liver abscess radiologically mimicking cystadenocarcinoma.

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A 72-old-year Japanese man was incidentally found to have out liver dysfunction on serum examination and a cystic tumor in the liver. Dynamic computed tomography revealed a solitary cystic tumor 14 cm in diameter with multiple septa. The cyst wall was occasionally irregular with hyperarterial

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

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

Unusual appendiceal pathology presenting as urologic disease.

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We report on 3 cases of unusual appendiceal pathology presenting as urologic disease: 2 cases were benign mucoceles and 1 a malignant mucocele or cystadenocarcinoma of the appendix. Two cases presented as pelvic masses causing urinary frequency and the third with fever and hydronephrosis. The

A case of oophoritis detected by gallium-67-citrate scintigraphy.

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A 39-year-old woman with fever of unknown origin was admitted to our hospital. Whole body scintigrams with 67Ga-citrate showed an abnormal accumulation of radioactivity in the pelvic cavity. Cystadenocarcinoma of the ovary was suspected on the basis of findings obtained by abdominal computed

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