Case Report
Copyright ©2009 The WJG Press and Baishideng. All rights reserved.
World J Gastroenterol. Aug 21, 2009; 15(31): 3947-3949
Published online Aug 21, 2009. doi: 10.3748/wjg.15.3947
Cavernous mesenteric lymphangiomatosis mimicking metastasis in a patient with rectal cancer: A case report
Seong Su Hwang, Hyun Joo Choi, Soo Youn Park
Seong Su Hwang, Soo Youn Park, Department of Radiology, St. Vincent’s Hospital, College of Medicine, The Catholic University of Korea, 93-1 Chi-dong, Paldal-gu, Suwon, Gyeonggi-do 442-023, South Korea
Hyun Joo Choi, Department of Pathology, St. Vincent’s Hospital, College of Medicine, The Catholic University of Korea, 93-1 Chi-dong, Paldal-gu, Suwon, Gyeonggi-do 442-023, South Korea
Author contributions: All authors contributed substantially in case collection, case analysis, and preparation of manuscript in this case report.
Correspondence to: Soo Youn Park, MD, Department of Radiology, St. Vincent’s Hospital, College of Medicine, The Catholic University of Korea, 93-1 Chi-dong, Paldal-gu, Suwon, Gyeonggi-do 442-023, South Korea. daladala@paran.com
Telephone: +82-31-2497486
Fax: +82-31-2475713
Received: April 25, 2009
Revised: July 17, 2009
Accepted: July 24, 2009
Published online: August 21, 2009
Abstract

Lymphangioma usually occurs in children and usually involves the skin. Mesenteric lymphangioma is extremely rare in adults. Typically, lymphangioma appears on computed tomography (CT) as a lower attenuation of a cystic mass, however, some cases appear to be a solid mass. We describe the CT and 18F-FDG positron emission tomography/CT appearance in a case of jejunal and mesenteric cavernous lymphangiomatosis mimicking metastasis in an adult patient with rectal cancer.

Keywords: Lymphangioma, Lymphangiomatosis, Mesentery, Small intestine, Computed tomography, 18F-FDG positron emission tomography/computed tomography