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Review
. 2011 May 12:2011:bcr0320114022.
doi: 10.1136/bcr.03.2011.4022.

Jejunal cavernous lymphangioma

Affiliations
Review

Jejunal cavernous lymphangioma

Gareth Morris-Stiff et al. BMJ Case Rep. .

Abstract

Cavernous lymphangiomas are usually identified in infants and children with the majority of lesions found around the head and neck, trunk or extremities. Tumours affecting the intra-abdominal organs are rare. The authors report a case of small bowel cavernous lymphangioma arising within the jejunum of a 34-year-old woman presenting with dyspnoea and anaemia, and review the existing literature relating to this uncommon tumour.

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Conflict of interest statement

Competing interests None.

Figures

Figure 1
Figure 1
Enteroscopic appearance of the lymphangioma.
Figure 2
Figure 2
This gross photograph of the segmental jejunal resection illustrates the striking multinodular and polypoid appearance of the jejunal lymphangioma, along with the entirely normal appearing adjacent jejunum.
Figure 3
Figure 3
The mucosa and submucosa are expanded and replaced by innumerable dilated lymphatics (arrows).
Figure 4
Figure 4
The jejunum adjacent to the lymphangioma was normal histologically, as illustrated here with intact villous architecture, mucosa and submucosa, lacking dilated lymphatic spaces. This feature excludes diffused lymphangiomatosis from the differential.
Figure 5
Figure 5
In addition to the mass forming lymphangioma occupying the wall of the jejunum, an additional focal mesenteric lymphangioma was identified in the resection specimen. The fibromuscular walls making up the lymphatic vessels and luminal benign lymphoid aggregates are illustrated.

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