GI Endoscopy · 2 min read

Epstein-Barr Virus (EBV) Lymphoproliferative Disorder Mimicking Watermelon Stomach (GAVE, Gastric Antral Vascular Ectasias)

A female patient in her mid-sixties presented with symptomatic iron deficiency anemia. Her hemoglobin was 5 gr/dl, MCV 75, low iron and ferritin levels. Her past medical history was remarkable for autoimmune hepatitis, perforated diverticulitis, peripheral artery disease, osteomyelitis and central nervous system lymphoma. Esophagogastroduodenoscopy (EGD) showed erythematous stomach mucosa, macroscopically resembling gastric antral vascular ectasia (GAVE or watermelon stomach) (Figure 1). Biopsies were obtained, followed by ablation of the suspected GAVE with argon plasma coagulation (APC).

Epstein Barr Virus (EBV) Lymphoproliferative Disorder Mimicking Watermelon Stomach (GAVE, Gastric Antral Vascular Ectasias)

by Klaus Mönkemüller, MD, PhD, FASGE, FJGES

Department of Gastroenterology, Carilion Memorial Hospital, Virginia Tech Carilion School of Medicine, Roanoke, USA

Figure 1. Epstein Barr Virus (EBV) Lymphoproliferative Disorder Mimicking Watermelon Stomach (GAVE, Gastric Antral Vascular Ectasias). A. Notice the multiple submucosal erythematous patches and prominent antral mucosal folds. B. The mucosa is obviously edematous. Panel C shows NBI.

The biopsy showed gastric mucosa with a dense lymphoid infiltrate with intermixed plasma cells, eosinophils, and histiocytes with a significant amount of edema, replacing and pushing the gastric mucosa. A significant portion of the lymphoid cells were CD79a positive with the same cells positive for EBV on an EBER in situ hybridization ancillary study. There were small aggregates of CD20 positive B-cells CD3 and CD5 and CD43 marked a select number of background T-cells. Immunohistochemistry for H. pylori negative. In sum, the histologic and ancillary studies support an unusual EBV positive B-cell lymphoproliferative disorder, with EBV positive B-cell lymphoma favored.

Epstein-Barr virus (EBV) has been linked to the development of a variety of human malignancies, including Burkitt's lymphoma, Hodgkin's disease, nasopharyngeal carcinoma, some T cell lymphomas (e.. g. NK/T), post-transplant lymphoproliferative disease, and more recently, certain cancers of the stomach, breast and smooth muscle (1-3). The oncogenic potential of EBV is related to its ability to infect and transform B lymphocytes into continuously growing lymphoblastoid cell lines (2). EBV encodes a series of products mimicking several growth, transcription and anti-apoptotic factors, to usurp control of the pathways that regulate diverse homeostatic cellular functions (2).

EBV-lymphoproliferative disorder may mimic inflammatory bowel disease (4, 5). Our case is unusual for two main reasons. First, the EBV-lymphoproliferative disorder mimicked GAVE. And second, there are very few reports in the literature of gastric EBV. It is important to keep EBV in mind as etiologic for a variety of neoplasias, including EBV-lymphoproliferative disorder

References

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About the author

Klaus Mönkemüller

Klaus Mönkemüller, MD, PhD, FASGE, FJGES, FESGE

Editor-in-Chief, The Practicing Endoscopist

Professor of Medicine, Carilion Memorial Hospital / Virginia Tech Carilion School of Medicine, Roanoke, Virginia, USA

Klaus Mönkemüller, MD, PhD, FASGE, FJGES, FESGE, is the editor-in-chief of The Practicing Endoscopist and the founder of EndoCollab. He is Professor of Medicine at Virginia Tech Carilion School of Medicine and a practicing endoscopist at Carilion Memorial Hospital in Roanoke, Virginia.

Dr. Mönkemüller has published extensively on endoscopic techniques and devices, with a particular focus on therapeutic endoscopy, foreign body removal, GI bleeding, and the use of caps and accessories in everyday practice. He lectures internationally and has contributed to multiple GI endoscopy textbooks and atlases.

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