scholarly journals Laparoscopic Resection of Rectal Cancer in a Patient with Double Inferior Vena Cava on Preoperative Computed Tomography—A Case Report—

Author(s):  
Satoshi HIRAHARA ◽  
Hironori KOBAYASHI ◽  
Kenji SHIRAKAWA ◽  
Yuta KUHARA ◽  
Haruna KUBOTA ◽  
...  
2020 ◽  
Vol 2020 (9) ◽  
Author(s):  
Akinobu Furutani ◽  
Sachiko Yoshida ◽  
Toshihiko Yoshida ◽  
Masayasu Nishi ◽  
Takashi Yamagishi ◽  
...  

Abstract We report the case of a patient with duplication of the inferior vena cava (DIVC) who underwent anterior laparoscopic resection for rectal cancer. A 66-year-old woman presented with abnormal lung shadows on a chest x-ray during a routine health checkup. She was diagnosed with rectal cancer and lung metastasis using colonoscopy and thoracoabdominal computed tomography (CT). In addition, a 3D CT angiography revealed double inferior vena cava, one on either side of the aorta. The preoperative diagnosis was rectal cancer cT3N0M1a(Lung) cStage IVA with DIVC, and a two-stage surgery was planned. The first stage was high anterior laparoscopic resection. This was safely performed because the pre-hypogastric nerve fascia was preserved and the left inferior vena cava was not visualized during the surgery. During the second stage of the surgery, video-assisted thoracoscopic left lower lobectomy was performed and no recurrence was observed for >6 months after the second surgery.


1970 ◽  
Vol 37 (1) ◽  
pp. 24-25
Author(s):  
Rampada Sarker ◽  
Asif Rahim ◽  
A Anisuzziman ◽  
SM Mahbubur ◽  
Sarwar Kamal ◽  
...  

DOI: 10.3329/bmj.v37i1.3605 Bangladesh Medical Journal 37(1) 2008 24-25


2013 ◽  
Vol 29 (7) ◽  
pp. 480-483 ◽  
Author(s):  
Xiaodong Wang ◽  
Zhengxin Chen ◽  
Qianrong Cai

Double inferior vena cava (DIVC) with deep venous thrombosis (DVT) is rare, and there is only one reported case of DIVC with DVT treated by catheter-directed thrombolysis. We report a case of a 32-year-old man with an extensive venous clot involving the infrarenal segment of a double IVC who received filter implantation and catheter-directed thrombolysis.


2019 ◽  
Vol 57 (219) ◽  
Author(s):  
Sagun Manandhar ◽  
Ashish Khanal

Supernumerary kidney is a rare clinical entity with fused supernumerary kidney being even rarer. Caudally located fused right supernumerary kidney with multiple nephrolithiasis was diagnosed in a 69-years-old lady by Computed Tomography Urography. A separate renal artery arising from the abdominal aorta as well as separate renal vein draining into the inferior vena cava was present along with right sided bifid collecting system. Embryological basis of origin of supernumerary kidney, its diagnosis, clinical significance and management are discussed.


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