| Literature DB >> 25943425 |
Konosuke Moritani1, Osamu Wada2, Heita Ozawa3, Shin Fujita4, Kenjiro Kotake5.
Abstract
BACKGROUND: Middle colic artery (MCA) aneurysms are very rare and exclusively reported with symptoms or rupture. We report successful laparoscopic elective surgery for both cecal cancer and MCA aneurysm in an 87-year-old man who presented with bloody stools.Entities:
Mesh:
Year: 2015 PMID: 25943425 PMCID: PMC4426541 DOI: 10.1186/s12957-015-0595-5
Source DB: PubMed Journal: World J Surg Oncol ISSN: 1477-7819 Impact factor: 2.754
Figure 1Preoperative computed tomography (CT) scan imaging (a) and CT angiography (b) showing a middle colic artery aneurysm (black arrow) measuring 10 × 7 mm without extravasation.
Figure 2Laparoscopic view of a middle colic artery (MCA) aneurysm (a). The MCA was ligated and divided at the root during radical right hemicolectomy with D3 lymph node dissection (b). acRCV, accessory right colic vein; GCT, gastrocolic trunk; MCA, middle colic artery; SMA, superior mesenteric artery; SMV, superior mesenteric vein.
Figure 3Resected Bormann type-2 cecal cancer specimen and shrunken middle colic artery aneurysm. (a) Both cecal cancer and aneurysm. (b) Aneurysm only.