Gastrointestinal Manifestations of CLOVES Syndrome

Author:

St-Pierre Joëlle1ORCID,Mirakhur Anirudh2,Forbes Nauzer13ORCID

Affiliation:

1. Division of Gastroenterology and Hepatology, Department of Medicine, University of Calgary, Calgary, Alberta, Canada

2. Department of Radiology, University of Calgary, Calgary, Alberta, Canada

3. Department of Community Health Sciences, University of Calgary, Calgary, Alberta, Canada

Abstract

ABSTRACT Congenital lipomatous overgrowth, vascular malformations, epidermal nevi, and scoliosis/skeletal/spinal anomalies (CLOVES) is a recently recognized syndrome. It is caused by somatic mutations in the PIK3CA gene that regulates cell growth and division. Although gastrointestinal manifestations of other PIK3CA-associated disorders have been described, they have not been well-characterized in CLOVES syndrome. We present a case report of a 34-year-old man with an established diagnosis of CLOVES syndrome who underwent a diagnostic colonoscopy for hematochezia and colonic wall thickening on imaging. Colonoscopy revealed widespread variceal-like submucosal lesions. Computed tomography/angiography showed the absence of the inferior mesenteric vein, impairing venous drainage.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

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