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Acute gastritis associated with enterovirus infection.

To the Editor.--We read with interest the article by Sepulveda and Patil. (1) Other than cytomegalovirus gastritis, viral infections of the stomach were not discussed in the article. Although enteroviruses were thought to be common causes of acute gastritis, few patients had endoscopies and biopsies to confirm the diagnosis. (2) Enteroviruses do not form intracellular inclusion bodies and could be easily missed by routine examination without special immunohistochemical stain. A lack of neutrophilic response may not rule out an acute enterovirus infection of the stomach because acute enterovirus meningitis is usually associated with lymphocyte-predominant pleocytosis. Immunoperoxidase staining for enteroviral capsid protein 1 (VP 1) allowed us to identify enterovirus infection in 82% of the stomach biopsies taken from 165 patients with chronic fatigue syndrome and chronic upper gastrointestinal symptoms, as compared with 20% of the control subjects. (3) Most of the biopsy specimens had minimal chronic inflammation by pathologic examination, and Helicobacter pylori was only demonstrated in 5% of the specimens.

We investigated the role of acute enterovirus infection in stomach biopsies taken from 20 immunocompetent patients (age 50 [+ or -] 22 years, 14 women, 6 men) who were hospitalized for severe vomiting and epigastric pain without known etiology after extensive laboratory and radiographic studies. Endoscopic examinations demonstrated minimal erythema or subepithelial hemorrhage in the antrum in 20 of 20 patients, and the pathologic examination showed mild, nonspecific, chronic inflammatory changes in 20 of 20 biopsies. Six of 20 (30%) had 1+ stainable enterovirus protein in the antrum (3); 13 of 20 (65%) had extensive staining (2+) of the specimens with only minimal chronic inflammation (Figure, A through D). Helicobacter pylori was seen in 2 of 20 samples (10%), but both patients also had positive enterovirus staining. All 20 specimens failed to stain with anti-cytomegalovirus monoclonal antibody of the same isotype. Two of 3 biopsy specimens grew enterovirus in cell culture, and 2 of 4 other specimens tested positive for viral RNA by reverse transcriptasepolymerase chain reaction, using previously described procedures. (3) Two of 8 perirectal swabs tested positive for enterovirus RNA. Stool cultures and examinations for ova and parasites were negative for all 20 patients. In contrast, 2 of 10 volunteers and 0 of 7 patients who had antrum biopsies for anemia, or gastropathy related to nonsteroidal antiinflammatory drug and alcohol, showed 2+ enterovirus staining. Interestingly, of the 2 volunteers who stained positive, one had recent history of cyclical vomiting and the other had chronic symptoms of gastroesophageal reflux. The difference between the patients and control group was statistically significant (P < .01, [chi square] test with Yate correction).

On follow-up, 17 of 19 patients had chronic, recurrent symptoms of epigastric pain, dyspepsia, nausea, anorexia, reflux, and bloating that lasted 3 months to more than 12 months. Five patients had cyclical vomiting; 1 patient was treated with parenteral hyperalimentation for at least 1 month after the hospitalization.

In the United States, at least 30 million people develop symptomatic enterovirus infection per year. (4) The most common route of transmission is oral fecal. Stomach is likely one of the first sites of viral replication because our previous study demonstrated chronic persistent infection in the stomach, (3) and enterovirus infection of animal stomach has been well documented by a recent study. (5) Although most cases of acute infection may be mild and self-limited, a significant number of patients develop severe, localized symptoms in the gastrointestinal tract requiring hospitalizations or outpatient evaluations. Proper diagnosis of acute enterovirus infection of the stomach may not only define one of the commonetiologies of acute gastritis but also help us approach chronic diseases that developed as the result of viral persistence. The findings of this article may provide the impetus for further studies on the role of enteroviruses in acute upper gastrointestinal illness.

[ILLUSTRATION OMITTED]

EV Med Research, LLC, holds a patent (US patent 7,579,144 B2) for diagnosing chronic fatigue syndrome using the procedure described herein.

(1.) Sepulveda A, Patil M. Practical approach to the pathologic diagnosis of gastritis. Arch Pathol Lab Med. 2008;132(10):1586-1593.

(2.) Dixon MF, Genta RM, Yardley JH, Correa P.

Classification and grading of gastritis: the updated Sydney system: international workshop on the histopathology of gastritis, Houston 1994. Am J Surg Pathol. 1996;20(10):1161-1181.

(3.) Chia JK, Chia AY. Chronic fatigue syndrome is associated with chronic enterovirus infection of the stomach. J Clin Pathol. 2008;61(1):43-48.

(4.) Oberste MS, Pallansch M. Establishing evidence for enterovirus infection in chronic diseases. Ann N Y Acad Sci. 2003;1005:23-31.

(5.) Kuss S, Etheredge C, Pfeiffer J. Multiple host barrier restrict poliovirus trafficking in mice. PLOS Pathog. 2008;4(6):e1000082.

John K. Chia, MD

Andrew Y. Chia, BS

EV Med Research, LLC

Lomita, CA 90717
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Title Annotation:Letters to the Editor
Author:Chia, John K.; Chia, Andrew Y.
Publication:Archives of Pathology & Laboratory Medicine
Article Type:Letter to the editor
Geographic Code:1USA
Date:Jan 1, 2010
Words:788
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