Embolization of Rectal Varices via a Paraumbilical Vein with an Abdominal Wall Approach in a Patient with Massive Ascites

2009 ◽  
Vol 20 (9) ◽  
pp. 1259-1261 ◽  
Author(s):  
Kenji Ibukuro ◽  
Kentaro Kojima ◽  
Ikutaro Kigawa ◽  
Rei Tanaka ◽  
Hozumi Fukuda ◽  
...  
2017 ◽  
Vol 2017 ◽  
pp. 1-3 ◽  
Author(s):  
Takuya Yamazaki ◽  
Yasushi Nagaba ◽  
Yoshitaka Shimada ◽  
Yoshinori Taoka ◽  
Satoru Minamida ◽  
...  

Urachal carcinoma is an extremely rare malignant tumor arising from the urachus in the fetus. We report a patient who developed urachal carcinoma 18 years after kidney transplantation. A 59-year-old man was admitted because of abdominal pain and massive ascites. He had undergone kidney transplantation 18 years earlier and had end-stage renal disease requiring dialysis. Abdominal CT showed massive ascites and an abdominal wall cystic mass separated from the peritoneal cavity. Hemodialysis was started, and paralytic ileus was diagnosed and treated. His ileus symptoms improved temporarily, but he died of myocardial infarction. An autopsy was performed, which revealed cystadenocarcinoma in the abdominal wall mass, leading to a diagnosis of urachal carcinoma.


1957 ◽  
Vol 33 (5) ◽  
pp. 830-836 ◽  
Author(s):  
R.A. MacHaffie ◽  
Robert L. Zaayer ◽  
Herbert Saichek ◽  
A.L. Sciortino

1966 ◽  
Vol 94 (6) ◽  
pp. 757-762 ◽  
Author(s):  
M. E. Chernosky
Keyword(s):  

MedPharmRes ◽  
2018 ◽  
Vol 2 (3) ◽  
pp. 22-26
Author(s):  
Uyen Vo ◽  
Duc Quach ◽  
Luan Dang ◽  
Thao Luu ◽  
Luan Nguyen

Budd–Chiari syndrome (BCS), a rare and life-threatening disorder due to hepatic venous outflow obstruction, is occasionally associated with hypoproteinemia. We herein report the first case of BCS with segmental obstruction of the intrahepatic portion of inferior vena cava (IVC) and hepatic veins (HVs) successfully treated by endovascular stenting in Vietnam. A 32-year-old female patient presented with a 2-month history of massive ascites and leg swelling. She refused history of oral contraceptives use. Hepatosplenomegaly without tenderness was noted. Laboratory data showed polycythemia, mild hypoalbuminemia and hypoproteinemia, slightly high total bilirubin and normal transaminase level. The serum ascites albumin gradient was 1.9 g/dL and ascitic protein level was 1.1 g/dL. The other data were normal. BCS was suspected because of the discrepancy between mild liver failure and massive ascites; and the presence of hepatosplenomegaly and polycythemia. On abdominal magnetic resonance imaging, the segmental obstruction of three HVs and IVC was 2-3 cm long without thrombus. Cavogram revealed the severe segmental stenosis of intrahepatic portion of IVC with no visualized HV and extensive collateral veins. A Protégé stent was deployed to IVC. Leg swelling and ascites were completely resolved within 3 days after stenting. During 1-year follow-up, edema was not recurred and repeated laboratory results were all normal.


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