Korean J Gastroenterol.  2016 Feb;67(2):116-118. 10.4166/kjg.2016.67.2.116.

Primary Intestinal Lymphangiectasia Diagnosed by Chylous Ascites

Affiliations
  • 1Department of Internal Medicine, Eulji University School of Medicine, Seoul, Korea. cyk@eulji.ac.kr
  • 2Department of Radiology, Eulji University School of Medicine, Seoul, Korea.
  • 3Department of Pathology, Eulji University School of Medicine, Seoul, Korea.

Abstract

No abstract available.


Figure

  • Fig. 1. Contrastenhanced abdomen CT. Nodularity of inner layer with mucosal enhancement of gastric antrum (white arrow), and ascites (black arrow) are seen.

  • Fig. 2. Ascites. There are gross milky color fluids obtained by paracentesis.

  • Fig. 3. Lymphangiography. There is no abrupt cut off sign or dermal back flow on lymphatic drainage.

  • Fig. 4. Enteroscopic findings. (A) Round elevated lesion with whitish paches. (B) After performing biopsies, white lymphatic fluid was seen flowing out from the biopsy site.

  • Fig. 5. Microscopic finding. The pathologic finding of proximal jejunal lesion shows dilated lymphatics containing proteinaceous fluid (H&E, ×200).


Reference

References

1. Wen J, Tang Q, Wu J, Wang Y, Cai W. Primary intestinal lymphangiectasia: four case reports and a review of the literature. Dig Dis Sci. 2010; 55:3466–3472.
Article
2. Vignes S, Bellanger J. Primary intestinal lymphangiectasia (Waldmann's disease). Orphanet J Rare Dis. 2008; 3:5.
Article
3. Umar SB, DiBaise JK. Protein-losing enteropathy: case illus-trations and clinical review. Am J Gastroenterol. 2010; 105:43–49.
Article
4. Oh TG, Chung JW, Kim HM, et al. Primary intestinal lymphangiectasia diagnosed by capsule endoscopy and double balloon enteroscopy. World J Gastrointest Endosc. 2011; 3:235–240.
Article
5. Rao R, Shashidhar H. Intestinal lymphangiectasia presenting as abdominal mass. Gastrointest Endosc. 2007; 65:522–523.
Article
6. Maamer AB, Baazaoui J, Zaafouri H, Soualah W, Cherif A. Primary intestinal lymphangiectasia or Waldmann's disease: a rare cause of lower gastrointestinal bleeding. Arab J Gastroenterol. 2012; 13:97–98.
Article
7. Imbesi V, Ciccocioppo R, Corazza GR. Long-standing intestinal lymphangiectasia detected by double-balloon enteroscopy. Clin Gastroenterol Hepatol. 2011; 9:e88–e89.
Article
8. Chamouard P, Nehme-Schuster H, Simler JM, Finck G, Baumann R, Pasquali JL. Videocapsule endoscopy is useful for the diagnosis of intestinal lymphangiectasia. Dig Liver Dis. 2006; 38:699–703.
Article
9. Filik L, Oguz P, Koksal A, Koklu S, Sahin B. A case with intestinal lymphangiectasia successfully treated with slow-release octreotide. Dig Liver Dis. 2004; 36:687–690.
Article
10. Suehiro K, Morikage N, Murakami M, Yamashita O, Hamano K. Late-onset primary intestinal lymphangiectasia successfully managed with octreotide: a case report. Ann Vasc Dis. 2012; 5:96–99.
Article
11. Zhu LH, Cai XJ, Mou YP, Zhu YP, Wang SB, Wu JG. Partial enter-ectomy: treatment for primary intestinal lymphangiectasia in four cases. Chin Med J (Engl). 2010; 123:760–764.
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