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Y. N. Ho, Y. P. Leong, A. S. Sakijan, M. Swaminathan and K. Sarvananthan, “Duodenal Leiomyosarcoma: A Report of a Rare and Aggressive Tumour,” Singapore Medical Journal, Vol. 33, No. 3, 1992, pp. 297-298.

has been cited by the following article:

• TITLE: Leiomyosarcoma of the Duodeno-Jejunal Angle: Two Case Reports and Literature Review

  AUTHORS: Hichem Jerraya, Ahmed Guirat, Foued Frikha, Issam Beyrouti

  KEYWORDS: Leiomyosarcoma; Duodenal Tumors; Surgery

  JOURNAL NAME: Surgical Science, Vol.4 No.7, June 28, 2013

  ABSTRACT: The duodenal leiomyosarcoma is a rare tumor. Its location in the duodenum makes diagnosis difficult and often delayed. Surgical treatment is not consensual because it must take into account anatomical imperatives which vary depending on the duodenal portion and oncological requirements that are not currently well known especially with regard to the utility of lymphadenectomy. We report 2 cases of leiomyosarcomas located at the angle of Treitz. This location is exceptional and only few cases were reported in the literature. From these 2 new cases and a review of the literature, we analyze the clinical features, diagnosis and treatment of duodenal leiomyosarcoma.