Copyright 2010 American Medical Association. All Rights Reserved. Applicable FARS/DFARS Restrictions Apply to Government Use.2010
Abdominal lymphangioma of the mesentery is an uncommon, benign neoplasm that primarily originates in the lymphatic system and presents as an abdominal mass. It is a rare lesion in the pediatric population; in 2 major pediatric surgical centers, only 19 and 22 cases were reported in a 25- and 34-year period, respectively.1,2 It is difficult to differentiate this tumor from a lymphatic cyst, which is due to a congenital defect in lymphatic development and is similar to lymphatic tumors that are found elsewhere (eg, cystic hygroma). Lymphangiomas, like cystic mesenteric tumors, may be unilocular or multilocular and have an endothelial lining with clear fluid contents. Most patients remain asymptomatic until the lesion exerts mass effect owing to its size (pressure sensation or postprandial fullness). Diagnosis is made by ultrasound or computed tomography, and in a few occurrences, prenatal ultrasonography.3 The differential diagnosis includes enterocele, dermoid, chylous, or serous retention cyst, traumatic cyst, and rarely, lymphangiosarcoma.
Management may pose a challenging therapeutic dilemma, as the rare patient may present with intestinal compromise, complicating the preoperative diagnosis. Intestinal torsion, volvulus, perforation with acute abdomen, and hemoperitoneum have been reported in association with abdominal lymphangioma.4- 6 Surgical removal by enucleation or excision is the only treatment, with resection of adjacent intestine if compromised. Incomplete resection can lead to recurrence and potentially malignant degeneration.7
Return to Quiz Case.
The Editor welcomes contributions to the Image of the Month. Manuscripts should be submitted via our online manuscript submission and review system (http://manuscripts.archsurg.com). Articles and photographs accepted will bear the contributor's name. Manuscript criteria and information are per the Instructions for Authors for Archives of Surgery (http://archsurg.ama-assn.org/misc/ifora.dtl). No abstract is needed, and the manuscript should be no more than 3 typewritten pages. There should be a brief introduction, 1 multiple-choice question with 4 possible answers, and the main text. No more than 2 photographs should be submitted. There is no charge for reproduction and printing of color illustrations.
Correspondence: R. Serene Perkins, MD, Clinical Assistant Professor, Director, International Surgery Program, Oregon Health & Science University, Department of Surgery, 3181 SW Sam Jackson Park Rd, L223, Portland, OR, 97239-3098 (email@example.com).
Accepted for Publication: April 27, 2009.
Author Contributions:Study concept and design: Perkins, and Lal. Acquisition of data: Perkins, Reddy. Analysis and interpretation of data: Perkins. Drafting of the manuscript: Perkins and Reddy. Critical revision of the manuscript for important intellectual content: Perkins and Lal. Statistical analysis: Reddy. Administrative, technical, and material support: Lal. Study supervision: Perkins.
Financial Disclosure: None reported.
Image of the Month—Diagnosis. Arch Surg. 2010;145(3):308. doi:10.1001/archsurg.2010.13-b