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Case Reports
. 2019 Feb 11:12:23-27.
doi: 10.2147/IMCRJ.S192940. eCollection 2019.

Pediatric localized intestinal lymphangiectasia treated with resection

Affiliations
Case Reports

Pediatric localized intestinal lymphangiectasia treated with resection

Judit Mari et al. Int Med Case Rep J. .

Abstract

Introduction: Primary intestinal lymphangiectasia (PIL) is a very rare disorder usually diagnosed before the third year of life or later in adulthood, presenting with pitting edema, hypoproteinemia and low immunoglobulin levels. The location and the extent of the affected bowel greatly influence the clinical manifestation. The localized or segmental form of PIL is extremely rare with only five pediatric cases reported worldwide.

Case presentation: A 10 year-old Caucasian boy presented with 3 months history of recurrent abdominal pain and a 1 month history of diarrhea. An ultrasound scan was performed on two separate occasions 10 days apart, revealing a growing cystic mass on the right side of the abdomen, in front of the psoas muscle. Subsequently an MRI scan confirmed that the mass originated from the mesenteries and infiltrates a short segment of the small bowel. Surgical resection of the affected segment was performed. Histopathological examination of the removed segment of ileum was consistent with intestinal lymphangiectasia. We could not identify any associated genetic syndromes or any other conditions that could have caused secondary intestinal lymphangiectasia. The patient's recovery from surgery was uneventful and no recurrence was observed in the following 4 years.

Conclusion: Despite being a benign condition, mortality of PIL can be as high as 13% due to the difficulties associated with the management of the disease. PIL should be considered as a rare but potential cause for an abdominal mass, even in the older child, when cystic mesenterial involvement might be seen on ultrasound or MRI. In selected cases of PIL affecting only a short segment of the bowel or following unsuccessful conservative treatment, surgical resection of the affected bowel segment can be curative.

Keywords: abdominal mass; abdominal pain; children; follow-up; surgery.

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Conflict of interest statement

Disclosure The authors report no conflicts of interest in this work.

Figures

Figure 1
Figure 1
Band-like cystic mass seen on the follow-up ultrasound.
Figure 2
Figure 2
MRI showed multilocular cystic mass involving the mesenteries.
Figure 3
Figure 3
Microscopic picture showing typical changes for PIL: dilated lymphatics in subserosa, submucosa and lamina propria. Note: Scale bars represent 500μm. Abbreviation: PIL, primary intestinal lymphangiectasia.

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References

    1. Vignes S, Bellanger J. Primary intestinal lymphangiectasia (Waldmann’s disease) Orphanet J Rare Dis. 2008;3(1):5. - PMC - PubMed
    1. Alshikho MJ, Talas JM, Noureldine SI, et al. Intestinal lymphangiectasia: insights on management and literature review. Am J Case Rep. 2016;17:512–522. - PMC - PubMed
    1. Levine C. Primary disorders of the lymphatic vessels—a unified concept. J Pediatr Surg. 1989;24(3):233–240. - PubMed
    1. Hokari R, Kitagawa N, Watanabe C, et al. Changes in regulatory molecules for lymphangiogenesis in intestinal lymphangiectasia with enteric protein loss. J Gastroenterol Hepatol. 2008;23(7 Pt 2):e88–e95. - PubMed
    1. Levitt DG, Levitt MD. Protein losing enteropathy: comprehensive review of the mechanistic association with clinical and subclinical disease states. Clin Exp Gastroenterol. 2017;10:147–168. - PMC - PubMed

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