Burkitt’s Lymphoma of the Gastrohepatic Omentum: A Malignant Presentation of Pseudoachalasia

Author:

Then Eric Omar1ORCID,Ofosu Andrew2,Rawla Prashanth3ORCID,Sunkara Tagore4ORCID,Dadana Sriharsha1,Culliford Andrea1,Gaduputi Vinaya1

Affiliation:

1. Division of Gastroenterology and Hepatology, SBH Health System, 4422 Third Ave, Bronx, New York 10457, USA

2. Division of Gastroenterology and Hepatology, The Brooklyn Hospital Center, Clinical Affiliate of The Mount Sinai Hospital, 121 Dekalb Ave, Brooklyn, NY 11201, USA

3. Department of Internal Medicine, Memorial Hospital of Martinsville and Henry County, 320 Hospital Drive Martinsville, VA 24115, USA

4. Division of Gastroenterology and Hepatology, Mercy Medical Center, 111 6th avenue Des Moines, IA 50314, USA

Abstract

Achalasia is an intrinsic disorder of the esophagus that results from loss of ganglion cells in the lower esophageal sphincter. Clinically it is manifested by dysphagia to solids and liquids, weight loss, regurgitation, and chest pain. Pseudoachalasia, in contrast, is a rare entity that causes identical symptoms, but has a divergent underlying pathogenesis. The symptomology in these cases oftentimes occurs secondary to extrinsic compression of the esophagus, mostly attributable to malignancy. Although many cases of extrinsic esophageal compression have been reported in the literature, rarely has this occurred secondary to Burkitt’s lymphoma in an adult. Here, we present a case of Burkitt’s lymphoma resulting in pseudoachalasia in a 70-year-old female. The concurrence of these two entities in one patient makes this case presentation especially rare.

Publisher

Hindawi Limited

Subject

General Engineering

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