CASE REPORT
A Case of Jejunal Mesenteric Liposarcoma, which Developed 5 Years after Resection of a Left Femoral Liposarcoma
Tsunaaki Sakakibara, Kenji Matsumoto, Katsuhiko Nouga, Isao Yokoyama, Masahiro Oogami, Hiroaki Fukagawa, Hiroaki Kitagawa, Yoshito Arisawa
Department of Surgery, Kawasaki City Hospital
A rare case of jejunal mesenteric liposarcoma, which developed 5 years after resection of a left femoral liposarcoma (myxoid type), is reported. A 49-year-old man was referred to our hospital with left abdominal pain. Computed tomographic findings showed a tumor originating in mesenteric soft tissues, and superior mesenteric arteriography revealed not a tumor stain but arterial encasement. Laparotomy revealed a jejunal mesenteric tumor about 40 cm distant from Treitz's ligament. The tumor was completely resected and histopathological findings indicated a liposarcoma (myxoid type). The postoperative course was uneventful. On the basis of the clinical course and laboratory data, this was believed to be a case of heterochronous double liposarcoma.
Key words
jejunal mesenteric liposarcoma, heterochronous double liposarcomas
Jpn J Gastroenterol Surg 24: 2791-2795, 1991
Reprint requests
Kenji Matsumoto Department of Surgery, Kawasaki City Hospital
Kawasaki City 210 JAPAN
Accepted
July 3, 1991
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