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[A Case of Cavernous Lymphangioma of the Small Bowel Mesentery].
Hong, In Taik; Cha, Jae Myung; Lee, Joung Il; Joo, Kwang Ro; Baek, Il Hyun; Shin, Hyun Phil; Jeon, Jung Won; Lim, Jun Uk.
Affiliation
  • Hong IT; Department of Internal Medicine, Kyung Hee University Hospital at Gangdong, Kyung Hee University School of Medicine, Seoul, Korea.
  • Cha JM; Department of Internal Medicine, Kyung Hee University Hospital at Gangdong, Kyung Hee University School of Medicine, Seoul, Korea.
  • Lee JI; Department of Internal Medicine, Kyung Hee University Hospital at Gangdong, Kyung Hee University School of Medicine, Seoul, Korea.
  • Joo KR; Department of Internal Medicine, Kyung Hee University Hospital at Gangdong, Kyung Hee University School of Medicine, Seoul, Korea.
  • Baek IH; Department of Internal Medicine, Kyung Hee University Hospital at Gangdong, Kyung Hee University School of Medicine, Seoul, Korea.
  • Shin HP; Department of Internal Medicine, Kyung Hee University Hospital at Gangdong, Kyung Hee University School of Medicine, Seoul, Korea.
  • Jeon JW; Department of Internal Medicine, Kyung Hee University Hospital at Gangdong, Kyung Hee University School of Medicine, Seoul, Korea.
  • Lim JU; Department of Internal Medicine, Kyung Hee University Hospital at Gangdong, Kyung Hee University School of Medicine, Seoul, Korea.
Korean J Gastroenterol ; 66(3): 172-5, 2015 Sep.
Article in Ko | MEDLINE | ID: mdl-26387702
Lymphangioma is a benign vascular lesion with characteristics of subepithelial tumor which can proliferate in the lymphatic system. Lymphangioma of the small-bowel mesentery is rare, having been reported in less than 2% of all lymphangiomas. Lymphangioma does not require any specific treatment because it is absolutely a benign tumor. However, surgical exploration is rarely required for cases with disease-related symptoms or complications, or for those misdiagnosed as a malignant lesion. We recently experienced a case of mesenteric cavernous lymphangomas in a 53-year-old female who was misdiagnosed as having a liposarcoma. The final diagnosis was confirmed by a pathologic examination of the specimen that was obtained via laparoscopic exploration. Herein, we report a very rare case of mesenteric cavernous lymphangioma along with a brief review of relevant literature.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Peritoneal Neoplasms / Lymphangioma Limits: Female / Humans / Middle aged Language: Ko Journal: Korean J Gastroenterol Journal subject: GASTROENTEROLOGIA Year: 2015 Document type: Article Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Peritoneal Neoplasms / Lymphangioma Limits: Female / Humans / Middle aged Language: Ko Journal: Korean J Gastroenterol Journal subject: GASTROENTEROLOGIA Year: 2015 Document type: Article Country of publication: