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A Giant Leiomyosarcoma of the Duodenum Y. Nimura 1 , T. Sato 2 , Y. Nakae 3 , Y. Yamamoto 4 , N. Nakashima 5 11st Dept. of Surg., Nagoya Univ., School of Medicine 2Dept. of Surg., Yachiyo Hospital 3Dept. of Internal Medicine, Yachiyo Hospital 42nd Dept. of Internal Medicine, Nagoya Univ., School of Medicine 5Dept. of Clinicalpathology, Nagoya Univ. Hospital pp.909-916
Published Date 1976/7/25
DOI https://doi.org/10.11477/mf.1403107336

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  • Abstract
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 A 54 year old man was seen on October 9, 1974, with complaints of slight anorexia and nausea. The pancreatic head or duodenal tumor was suspected from an X-ray examination of the upper G-I tract. A diagnosis of a malignant tumor of the duodenum was made from hypotonic duodenography, barium enema, drip infusion cholangiography, superior mesenteric arteriography, and endoscopic retrograde cholangiopancreatography. Duodenofiberscopy also revealed a large ulceration at the anal side of Papilla Vateri and a few biopsied specimens were taken from the lesion. Histological diagnosis was leiomyosarcoma.

 On November 15, 1974, the operation was performed. We noticed a liver metastasis in the right hepatic lobe and a lymphnode metastasis in the mesenteric root, and performed panceaticoduodenectomy, cholecystectomy, right hemicolectomy, partial jejunectomy and partial right hepatectomy. In the resected specimens, the tumor, 12×11×11.5 cm in size, was situated at the anal side of Papilla Vateri and had an exenteric growth toward the pancreatic head and body.

 Leiomyosarcoma of the duodenum is an uncommon malignant tumor and the first case was reported by Von Salis in 1920. McBrien reported 95 cases in 1971. In our country,84 cases were reported from 1939 to 1974. We have referred to the literature of leiomyosarcoma of the duodenum.


Copyright © 1976, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1219 印刷版ISSN 0536-2180 医学書院

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