Literature DB >> 36061251

Isolated Colonic Lymphangiectasia Secondary to Submucosal Injection.

Sanjeevani Tomar1, Emad Alqassim2, Sultan Mahmood3.   

Abstract

Entities:  

Year:  2022        PMID: 36061251      PMCID: PMC9433060          DOI: 10.14309/crj.0000000000000853

Source DB:  PubMed          Journal:  ACG Case Rep J        ISSN: 2326-3253


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CASE REPORT

An 81-year-old woman with a medical history of tobacco use and family history of colon cancer was referred for colonoscopy because of a reported weight loss of 25 pounds over 10 months. Colonoscopy revealed a 15 mm flat polyp in the ascending colon with a mucus cap (Figure 1). A submucosal injection of ORISE gel revealed a large whitish discoloration of the mucosa encompassing the polyp and surrounding mucosa (Figure 2). The polyp was removed with a cold snare in a piecemeal manner. Biopsy specimens of the surrounding mucosa revealed dilated lymphatics (4× magnification, hematoxylin and eosin stain) (Figure 3), which were interpreted as isolated colonic lymphangiectasia secondary to submucosal injection.
Figure 1.

Flat polyp in the ascending colon with a mucus cap.

Figure 2.

Large whitish discoloration of the mucosa encompassing the polyp and surrounding mucosa after submucosal injection with ORISE gel.

Figure 3.

Colonic specimen (4× magnification, hematoxylin and eosin stain) showing dilated lymphatics.

Flat polyp in the ascending colon with a mucus cap. Large whitish discoloration of the mucosa encompassing the polyp and surrounding mucosa after submucosal injection with ORISE gel. Colonic specimen (4× magnification, hematoxylin and eosin stain) showing dilated lymphatics. Primary intestinal lymphangiectasia is a rare disease of an unknown worldwide incidence that primarily affects the small intestine in children younger than 3 years, usually with other congenital abnormalities.[1] However, it is increasingly being recognized in adults because of direct visualization of the small bowel with imaging modalities, such as capsule endoscopy and double-balloon enteroscopy.[2,3] Isolated colonic lymphangiectasias are even more rare, and their clinical significance in an asymptomatic patient is unclear.

DISCLOSURES

Author contributions: S. Tomar wrote and edited the article, reviewed the literature, and is the article guarantor. E. Alqassim provided the images and revised the article for intellectual content. S. Mahmood provided the images and critically reviewed the article. All authors approved the final version of the manuscript. Financial disclosures: None to report. Informed consent was obtained for this case report.
  3 in total

1.  Primary intestinal lymphangiectasia diagnosed by capsule endoscopy and double balloon enteroscopy.

Authors:  Tak Geun Oh; Joo Won Chung; Hee Man Kim; Seok-Joo Han; Jin Sung Lee; Jung Yeob Park; Si Young Song
Journal:  World J Gastrointest Endosc       Date:  2011-11-16

Review 2.  Primary intestinal lymphangiectasia in an adult patient: A case report and review of literature.

Authors:  Rudolf Huber; Georg Semmler; Alexander Mayr; Felix Offner; Christian Datz
Journal:  World J Gastroenterol       Date:  2020-12-08       Impact factor: 5.742

Review 3.  Primary intestinal lymphangiectasia (Waldmann's disease).

Authors:  Stéphane Vignes; Jérôme Bellanger
Journal:  Orphanet J Rare Dis       Date:  2008-02-22       Impact factor: 4.123

  3 in total

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