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Chapter 13 - Types of Gastritis

Published online by Cambridge University Press:  06 June 2020

Roger M. Feakins
Affiliation:
Royal Free London NHS Foundation Trust, London, UK
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Summary

Biopsies of gastric mucosa, obtained at endoscopy, are common in routine pathology practice. The material ranges from single random biopsies of macroscopically normal or near-normal mucosa to detailed series mapping processes such as atrophic gastritis. In practice, the majority of cases will fall into the normal/near-normal mucosa, reactive gastritis, or Helicobacter pylori-associated gastritis categories. In this chapter, a practical, systematic approach to reporting gastric biopsies is emphasised to ensure that the pathology report assists in patient management. Three common systems for classification of gastritis – Sydney, ICD-10, Kyoto – are summarised and the key features required in the pathology report discussed. An approach to the differential diagnosis of some commonly encountered histological findings/patterns of mucosal injury, including atrophic gastritis, lymphocytic gastritis, and ‘granulomas’, is provided. There is discussion of the appropriate use of histochemistry/immunohistochemistry in gastric biopsies, noting that ‘routine specials’ add little to the assessment of H&E sections in most cases. Finally, the need for accurate clinical information (including endoscopic appearances, sites of biopsy, medical history and current/previous medications) to aid interpretation of the morphological findings and of the results of ancillary investigations is considered.

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Non-Neoplastic Pathology of the Gastrointestinal Tract
A Practical Guide to Biopsy Diagnosis
, pp. 186 - 205
Publisher: Cambridge University Press
Print publication year: 2020

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References

Goldenring, JR, Nam, KT, Wang, TC, et al. Spasmolytic polypeptide-expressing metaplasia and intestinal metaplasia: time for re-evaluation of metaplasias and the origins of gastric cancer. Gastroenterology. 2010;138:2207–10.Google Scholar
Lee, JY, Kim, N, Lee, HS, et al. Correlations among endoscopic, histologic and serologic diagnoses for the assessment of atrophic gastritis. J Cancer Prev. 2014;19:4755.CrossRefGoogle ScholarPubMed
Kobayashi, M, Yamaguchi, O, Nagata, K, et al. Acute haemorrhagic gastritis after nivolumab treatment. Gastrointest Endosc. 2017; 86:915–6.CrossRefGoogle ScholarPubMed
Laine, L, Weinstein, WM. Histology of alcoholic haemorrhagic ‘gastritis’: a prospective evaluation. Gastroenterology. 1988;94:1254–62.Google Scholar
Castellano, VM, Munoz, MT, Colina, F, et al. Collagenous gastrobulbitis and collagenous colitis: case report and review of the literature.Scand J Gastroenterol. 1999;34:632–8.Google Scholar
Ma, C, Park, JY, Montgomery, EA, et al. A comparative clinicopathologic study of collagenous gastritis in children and adults: the same disorder with associated immune-mediated diseases. Am J Surg Pathol. 2015;39:802–12.Google Scholar
Arnason, T, Brown, IS, Goldsmith, JD, et al. Collagenous gastritis: a morphologic and immunohistochemical study of 40 patients. Mod Pathol. 2015;28:533–44.CrossRefGoogle ScholarPubMed
Blackshaw, AJ, Levison, DA. Eosinophil infiltrates of the gastrointestinal tract. J Clin Pathol. 1986;39:17.CrossRefGoogle ScholarPubMed
Goldman, H, Proujansky, R. Allergic proctitis and gastroenteritis in children:clinical and mucosal biopsy features in 53 cases. Am J Surg Pathol. 1986;10:7586.Google Scholar
Lwin, T, Melton, SD, Genta, RM. Eosinophilic gastritis: histopathological characterization and quantification of the normal gastric eosinophil content. Mod Pathol. 2011;24:556–63.CrossRefGoogle ScholarPubMed
Hurrell, JM Genta, RM, Melton, SD. Histopathologic diagnosis of eosinophilic conditions in the gastrointestinal tract. Adv Anat Pathol. 2011;18:335–48.CrossRefGoogle ScholarPubMed
Ko, HM, Morotti, RA, Yershov, O, Chehade, M. Eosinophilic gastritis in children: clinicopathological correlation, disease course and response to therapy. Am J Gastroenterol. 2014;109:1277–85.CrossRefGoogle ScholarPubMed
Oberhuber, G, Puspok, A, Oesterreicher, C, et al. Focally enhanced gastritis: a frequent type of gastritis in patients with Crohn’s disease. Gastroenterology. 1997;112:698706.Google Scholar
Brown, IS, Miller, GC, Bettington, ML, et al. Histopathological findings of extra-ileal manifestations at initial diagnosis of Crohn’s disease-related ileitis. Virchows Arch. 2016;469:515–22.CrossRefGoogle ScholarPubMed
Xin, W, Greenson, JK. The clinical significance of focally enhanced gastritis. Am J Surg Pathol. 2004;28:1347–51.CrossRefGoogle ScholarPubMed
McHugh, JB, Gopal, P, Greenson, JK. The clinical significance of focally enhanced gastritis. Am J Surg Pathol. 2013;37:295–9.Google Scholar
Horje, CSHT, Meijer, J, Rovers, L, et al. Prevalence of upper gastrointestinal lesions at primary diagnosis in adults with inflammatory bowel disease. Inflamm Bowel Dis. 2016;22:18961901.Google Scholar
Sharif, F, McDermott, M, Dillon, M, et al. Focally enhanced gastritis in children with Crohn’s disease and ulcerative colitis. Am J Gastroenterol. 2002;97:1415–20.CrossRefGoogle ScholarPubMed
Ectors, NL, Dixon, MF, Gebboes, KJ, et al. Granulomatous gastritis: a morphological and diagnostic approach. Histopathology. 1993;23:5561.CrossRefGoogle ScholarPubMed
Shapiro, JL, Goldblum, JR, Petras, RE. A clinicopathologic study of 42 patients with granulomatous gastritis. Is there really an ‘idiopathic’ granulomatous gastritis? Am J Surg Pathol. 1996;20:462–70.Google Scholar
Miyamoto, M, Haruma, K, Yoshihara, M, et al. Isolated granulomatous gastritis successfully treated by Helicobacter pylori eradication: a possible association between granulomatous gastritis and Helicobacter pylori. J Gastroenterol. 2003;38:371–5.CrossRefGoogle ScholarPubMed
Maeng, L, Lee, A, Choi, K, et al. Granulomatous gastritis: a clinicopathologic analysis of 18 biopsy cases. Am J Surg Pathol. 2004;28:941–5.CrossRefGoogle ScholarPubMed
Sandmeier, D, Bouzourene, H. Does idiopathic granulomatous gastritis exist? Histopathology. 2005;46:352–3.Google Scholar
Lash, RH, Lauwers, GY, Odze, RD, Genta, RM. Inflammatory disorders of the stomach. In Odze, RD, Goldblum, JR (eds), Surgical Pathology of the GI Tract, Liver, Biliary Tract and Pancreas,3rd ed. Philadelphia: Saunders Elsevier; 2015, 352–81.Google Scholar
Brown, I, Kumarasinghe, MP. Granulomas in the gastrointestinal tract: deciphering the Pandora’s box. Virchows Arch. 2018;472:3–14.CrossRefGoogle Scholar
Casey, KM, Quigley, TM, Kozarek, RA, et al. Lethal nature of ischaemic gastropathy. Am J Surg. 1993;165:646–9.Google Scholar
Elwir, S, Shaukat, A, Mesa, H, et al. Ischaemic gastritis: a multicenter case series of a rare clinical entity and a review of the literature. J Clin Gastroenterol. 2016;50:722–6.Google Scholar
Tang, SJ, Daram, SR, Wu, R, et al. Pathogenesis, diagnosis, and management of gastric ischaemia. Clin Gastroenterol Hepatol. 2014;12:246–52.Google Scholar
Sharma, A, Mukewar, S, Chari, ST, et al. Clinical features and outcomes of gastric ischemia. Dig Dis Sci. 2017;62:3550–5.CrossRefGoogle ScholarPubMed
Katz, J, Brar, S, Sidhu, JS. Histopathological characterization of a Cameron lesion. Int J Surg Pathol. 2012;20:528–30.Google Scholar
Haot, J, Hamichi, L, Wallez, L, et al. Lymphocytic gastritis: a newly described entity: a retrospective endoscopic and histological study. Gut. 1988;29:1258–64.Google Scholar
Lebwohl, B, Green, PH, Genta, RM. The coeliac stomach: gastritis in patients with coeliac disease. Aliment Pharmacol Ther. 2015;42:180–7.CrossRefGoogle ScholarPubMed
Dixon, MF, Wyatt, JI, Burke, DA, et al. Lymphocytic gastritis: relationship to Campylobacter pylori infection. J Pathol. 1988;154:125–32.Google Scholar
Wu, TT, Hamilton, SR. Lymphocytic gastritis; association with the aetiology and topology. Am J Surg Pathol. 1999;23:153–8.CrossRefGoogle ScholarPubMed
Brown, IS, Smith, J, Rosty, C. Gastrointestinal pathology in celiac disease: a case series of 150 consecutive newly diagnosed patients. Am J Clin Pathol. 2012;138:42–9.Google Scholar
Hayat, M, Arora, DS, Wyatt, JI, et al. The pattern of involvement of the gastric mucosa in lymphocytic gastritis is predictive of the presence of duodenal pathology. J Clin Pathol. 1999;52:815–9.CrossRefGoogle ScholarPubMed
Nielsen, JA, Roberts, CA, Lager, DJ, et al. Lymphocytic gastritis is not associated with active Helicobacter pylori infection. Helicobacter. 2014;19:349–55.CrossRefGoogle Scholar
Lynch, DA, Sobala, GM, Dixon, MF, et al. Lymphocytic gastritis and associated small bowel disease: a diffuse lymphocytic gastroenteropathy? J Clin Pathol. 1995;48:939–45.Google Scholar
Dixon, MF, Genta, RM, Yardley, JH, Correa, P. Classification and grading of gastritis; the updated Sydney System. Am J Surg Pathol. 1996;20:1161–81.CrossRefGoogle ScholarPubMed
Rubio-Tapia, A, Herman, ML, Ludvigsson, JF, et al. Severe spruelike enteropathy associated with olmesartan. Mayo Clin Proc. 2012;87:732–8.CrossRefGoogle ScholarPubMed
Gabrieli, D, Ciccone, F, Capannolo, A, et al. Subtypes of chronic gastritis in patients with celiac disease before and after gluten-free diet. United European Gastroenterol J. 2017;5:805–10.Google Scholar
Van Noord, D, Biermann, K, Moons, LM, et al. Histological changes in patients with chronic upper gastrointestinal ischaemia. Histopathology. 2010;57:615–21.Google Scholar
Dixon, MF, O’Connor, HJ, Axon, AT, et al. Reflux gastritis: distinct histopathological entity? J Clin Pathol. 1986;39:524–30.CrossRefGoogle ScholarPubMed
Wolf, EM, Plieschnegger, W, Schmack, B, et al. Evolving patterns in the diagnosis of reactive gastropathy: data from a prospective Central European multicenter study with proposal of a new histologic scoring system. Pathol Res Pract. 2014;210:847–54.Google Scholar
Sobala, GM, O’Connor, HJ, Dewar, EP, et al. Bile reflux and intestinal metaplasia in gastric mucosa. J Clin Pathol. 1993;46:235–40.Google Scholar
Mino-Kenudson, M, Tomita, S, Lauwers, GY. Mucin expression in reactive gastropathy: an immunohistochemical analysis. Arch Pathol Lab Med. 2007;131:8690.CrossRefGoogle ScholarPubMed
Abraham, SC, Singh, VK, Yardley, JH, et al. Hyperplastic polyps of the stomach: associations with histologic patterns of gastritis and gastric atrophy. Am J Surg Pathol. 2001;25:500–7.Google ScholarPubMed
Tazawa, K, Tsutsumi, Y. Localized accumulation of Russell body-containing plasma cells in gastric mucosa with Helicobacter pylori infection: ‘Russell body gastritis’. Pathol Int. 1998;48:242–4.Google Scholar
Zhang, H, Jin, Z, Cui, R. Russell body gastritis/duodenitis: a case series and description of immunoglobulin light chain restriction. Clin Res Hep Gastrotenterol. 2014;38:e8997.Google Scholar
Yorita, K, Iwasaki, T, Uchita, K, et al. Russell body gastritis with Dutcher bodies evaluated using magnification endoscopy. World J Gastrointest Endosc. 2017;9:417–24.Google Scholar
Shinozaki, A, Ushiku, T, Fukayama, M. Prominent Mott cell proliferation in Epstein-Barr virus-associated gastric carcinoma. Hum Pathol. 2010;41:134–8.Google Scholar
Wolf, EM, Mrak, K, Tschmelitsch, J, et al. Signet ring cell cancer in a patient with Russell body gastritis: a possible diagnostic pitfall. Histopathology. 2011;58:1173–82.Google Scholar
Guarino, M, Reale, D, Micoli, G, et al. Xanthogranulomatous gastritis associated with xanthogranulomatous cholecystitis. J Clin Pathol. 1993;46:8890.Google Scholar
Okamura, A, Takahashi, T, Saikawa, Y, et al. Xanthogranulomatous gastritis of the remnant stomach mimicking a malignant tumor: a case report. Oncol Lett. 2016;11:1453–6.Google Scholar
Coati, I, Fassan, M, Farinati, F, et al. Autoimmune gastritis: pathologist’s viewpoint. World J Gastroenterol. 2015;21:12179–89.CrossRefGoogle ScholarPubMed
Centanni, M, Marignani, M, Gargano, L, et al. Atrophic body gastritis in patients with autoimmune thyroid disease: an underdiagnosed association. Arch Intern Med. 1999;159:1726–30.CrossRefGoogle ScholarPubMed
Torbenson, M, Abraham, SC, Boitnott, J, et al. Autoimmune gastritis: distinct histological and immunohistochemical findings before complete loss of oxyntic glands. Mod Pathol. 2002;15:102–9.Google Scholar
Jhala, NC, Montemor, M, Jhala, D, et al. Pancreatic acinar cell metaplasia in autoimmune gastritis. Arch Pathol Lab Med. 2003;127:854–7.CrossRefGoogle ScholarPubMed
Solcia, E, Fiocca, T, Villani, L, et al. Morphology and pathogenesis of endocrine hyperplasias, pre-carcinoid lesions, and carcinoids arising in chronic atrophic gastritis. Scand J Gastroenterol. 1991;26(Suppl 180):146–59.CrossRefGoogle Scholar
Park, JY, Cornish, TC, Lam-Himlin, D, et al. Gastric lesions in patients with autoimmune metaplastic atrophic gastritis (AMAG) in a tertiary care setting. Am J Surg Pathol. 2010;34:1591–8.Google Scholar
Krasinskas, AM, Abraham, SC, Metz, DC, Furth, EE. Oxyntic mucosa pseudopolyps: a presentation of atrophic autoimmune gastritis. Am J Surg Pathol. 2003;27:236–41.Google Scholar
Vieth, M, Kushima, R, Borchard, F, et al. Pyloric gland adenoma: a clinicopathological analysis of 90 cases. Virchows Arch. 2003;442:317–21.CrossRefGoogle ScholarPubMed
Murphy, G, Dawsey, SM, Engels, EA, et al. Cancer risk after pernicious anaemia in the US elderly population. Clin Gastroenterol Hepatol. 2015;13:2282–9.CrossRefGoogle ScholarPubMed
Kuipers, EJ. Pernicious anaemia, atrophic gastritis, and the risk of cancer. Clin Gastroenterol Hepatol. 2015;13:2290–2.Google Scholar
Rugge, M, Fassan, M, Pizzi, M, et al. Autoimmune gastritis: histology phenotype and OLGA staging. Aliment Pharmacol Ther. 2012;35:1460–6.Google Scholar
Zhang, Y, Weck, MN, Schottker, B, et al. Gastric parietal cell antibodies, Helicobacter pylori infection, and chronic atrophic gastritis: evidence from a large population-based study in Germany. Cancer Epidemiol Biomarkers Prev. 2013;22:821–6.CrossRefGoogle ScholarPubMed
Notohara, K, Kamisawa, T, Uchida, K, et al. Gastrointestinal manifestation of immunoglobulin G4-related disease: clarification through a multicenter survey. J Gastroenterol. 2018;53:845–53.Google Scholar
Jevremovic, D, Torbenson, M, Murray, JA, Burgart, LJ, Abraham, SC. Atrophic autoimmune pangastritis: a distinctive form of antral and fundic gastritis associated with systemic autoimmune disease. Am J Surg Pathol. 2006;30:1412–9.Google Scholar
Singhi, AD, Goyal, A, Davison, JM, Regueiro, MD, Roche, RL, Ranganathan, S. Pediatric autoimmune enteropathy: an entity frequently associated with immunodeficiency disorders. Mod Pathol. 2014;27:543–53.Google Scholar
Chen, SY, Zhang, RG, Duan, GC. Pathogenic mechanisms of the oncoprotein CagA in H. pylori-induced gastric cancer. Oncol Rep. 2016;36:3087–94.Google Scholar
Chmiela, M, Karwowska, Z, Gonciarz, W, et al. Host pathogen interactions in Helicobacter pylori related gastric cancer. World J Gastroenterol. 2017;23:1521–40.CrossRefGoogle ScholarPubMed
Leja, M, Axon, A, Brenner, H. Epidemiology of Helicobacter pylori infection. Helicobacter. 2016;21(Suppl 1):37.Google Scholar
Burkitt, MD, Duckworth, CA, Williams, JM, Pritchard, DM. Helicobacter pylori-induced gastric pathology: insights from in vivo and ex vivo models. Dis Model Mech. 2017;10:89104.CrossRefGoogle ScholarPubMed
Romero-Flores, JL, Fernandez-Rivero, JA, Marroquín-Fabian, E, et al. Diagnostic accuracy of nodular gastritis for H. pylori infection. Ther Clin Risk Manag. 2016;13:914.Google Scholar
Kuipers, EJ, Lundell, L, Klinkenberg-Knol, EC, et al. Atrophic gastritis and Helicobacter pylori infection in patients with reflux oesophagitis treated with omeprazole or fundoplication. N Engl J Med. 1996;334:1018–22.CrossRefGoogle ScholarPubMed
Attumi, TA, Graham, DY. Follow-up testing after treatment of Helicobacter pylori infections: cautions, caveats, and recommendations. Clin Gastroenterol Hepatol. 2011;9:373–5.Google Scholar
Beg, S, Ragunath, K, Wyman, A, et al. Quality standards in upper gastrointestinal endoscopy: a position statement of the British Society of Gastroenterology (BSG) and Association of Upper Gastrointestinal Surgeons of Great Britain and Ireland (AUGIS). Gut. 2017;66:1886–99.Google Scholar
Horvath, B, Pai, RK. Prevalence of Helicobacter pylori in gastric hyperplastic polyps. Int J Surg Pathol. 2016;24:704–8.Google Scholar
Decker, L, Routh, JK, Snider, JS, et al. Selective staining of gastric biopsies for H. pylori does not affect detection rates or turnaround time and improves cost compared to reflexive staining. Pathol Res Pract. 2017;213:23–6.Google Scholar
Bhakta D, , Graham, DY, Chan, J, et al. Lessons from using culture-guided treatment after referral for multiple treatment failures for Helicobacter pylori infection. Clin Gastroenterol Hepatol. 2018;16:1531–2.Google Scholar
Kiss, S, Zsikla, V, Frank, A, et al. Helicobacter-negative gastritis: polymerase chain reaction for Helicobacter DNA is a valuable tool to elucidate the diagnosis. Aliment Pharmacol Ther. 2016;43:924–32.Google Scholar
Genta, RM, Lash, RH. Helicobacter pylori-negative gastritis: seek, yet ye shall not always find. Am J Surg Pathol. 2010;34:e2534.Google Scholar
Mach, T, Skwara, P, Biesiada, G, et al. Morphological changes of the upper gastrointestinal tract mucosa and Helicobacter pylori infection in HIV-positive patients with severe immunodeficiency and symptoms of dyspepsia. Med Sci Monit. 2007;13:CR149.Google Scholar
Yakoob, J, Abbas, Z, Khan, R, et al. Prevalence of non Helicobacter pylori species in patients presenting with dyspepsia. BMC Gastroenterol. 2012;12:3.Google Scholar
Hansen, SK, Pottorf, BJ, Hollis, HW Jr, et al. Is it necessary to perform full pathologic review of all gastric remnants following sleeve gastrectomy? Am J Surg. 2017;214:1151–5.Google ScholarPubMed
Rath-Wolfson, L, Varona, R, Bubis, G, et al. Gastritis in patients undergoing sleeve gastrectomy: prevalence, ethnic distribution, and impact on glycemic control. Medicine (Baltimore). 2017;96:e6602.Google Scholar
Moosvi, AR, Saravolatz, LD, Wong, DH, et al. Emphysematous gastritis: case report and review. Rev Infect Dis. 1990;12:848–55.Google Scholar
Watson, A, Bul, V, Staudacher, J, et al. The predictors of mortality and secular changes in management strategies in emphysematous gastritis. Clin Res Hep Gastroenterol. 2017;41:e1e7.Google Scholar
Matsushima, K, Won, EJ, Tangel, MR, et al. Emphysematous gastritis and gastric emphysema: similar radiographic findings, distinct clinical entities. World J Surg. 2015;39:1008–17.Google Scholar
Miller, AI, Smith, B, Rogers, AI. Phlegmonous gastritis. Gastroeterology. 1975;68:231–8.Google Scholar
O’Toole, PA, Morris, JA. Acute phlegmonous gastritis. Postgrad Med J. 1988;64:315–16.CrossRefGoogle ScholarPubMed
Min, SY, Kim, YH, Park, WS. Acute phlegmonous gastritis complicated by delayed perforation. World J Gastroenterol. 2014;20:3383–7.CrossRefGoogle ScholarPubMed
Garcia, F, Garau, J, Sierra, M, et al. Cytomegalovirus mononucleosis-associated antral gastritis simulating malignancy. Arch Intern Med. 1987;147:787–8.CrossRefGoogle ScholarPubMed
Aqel, NM, Tanner, P, Drury, A, et al. Cytomegalovirus gastritis with perforation and gastrocolic fistula formation. Histopathology. 1991;18:165–8.Google Scholar
Megged, O, Schlesinger, Y. Cytomegalovirus-associated protein-losing gastropathy in childhood. Eur J Pediatr. 2008:167:1217–2.Google Scholar
Nelson, AC, Crippin, JS. Gastritis secondary to herpes simplex virus. Am J Gastroenterol. 1997;92:2116–17.Google Scholar
Nohr, EW, Itani, DM, Andrews, CN, et al. Varicella-zoster virus gastritis: case report and review of the literature. Int J Surg Pathol. 2017;25:449–52.Google Scholar
Toll, AD, Malik, S, Tuluc, M. Ulcerative gastritis secondary to Epstein-Barr viral infection. Dig Dis Sci. 2010;55:218–19.Google Scholar
Sujino, T, Ebinuma, H, Hosoe, N, et al. Epstein-Barr virus-associated gastritis: a case report. Dig Dis Sci. 2013;58:883–6.Google Scholar
Minoli, G, Terruzzi, V, Butti, G, et al. Gastric candidiasis: an endoscopic and histological study in 26 patients. Gastrointest Endosc. 1982;28:5961.Google Scholar
Sari, R, Altunbas, H, Mahsereci, E, et al. Multiple gastric ulcers caused by gastric candidiasis in a diabetic patient: a rare cause of upper GI bleeding. Gastrointest . Endosc 2003;58:309–11.Google Scholar
Katzenstein, ALA, Maksem, J. Candidal infection of gastric ulcers: histology, incidence, and clinical significance. Am J Clin Pathol. 1979;71:137–41.Google Scholar
Spelberg, B. Gastrointestinal mucormycosis: an evolving disease. Gastroenterol Hepatol (NY). 2012;8:140–2.Google Scholar
Fisher, JR, Sanowski, RA. Disseminated histoplasmosis producing hypertrophic gastric folds. Am J Dig Dis.1978;23:282–5.Google Scholar
Lamps, LW, Molina, CP, West, AB, et al The pathologic spectrum of gastrointestinal and hepatic histoplasmosis. Am J Clin Pathol. 2000;113:6472.CrossRefGoogle ScholarPubMed
Bonacini, M, Nussbaum, J, Ahluwalia, C. Gastrointestinal, hepatic and pancreatic involvement with Cryptococcus neoformans in AIDS. J Clin Gastroenterol. 1990;12:295–7.Google Scholar
Washington, K, Gottfried, MR, Wilson, ML. Gastrointestinal cryptococcosis. Mod Pathol. 1991;4:707–11.Google ScholarPubMed
Dieterich, DT, Lew, EA, Bacon, DJ, et al. Gastrointestinal pneumocystosis in HIV-infected patients on aerosolized pentamidine: report of five cases and literature review. Am J Gastroenterol. 1992;87:1763–70.Google Scholar
Rivasi, F, Rossi, P, Righi, E, et al. Gastric cryptosporidiosis: correlation between intensity of infection and histological alterations. Histopathology. 1999;34:405–9.Google Scholar
Peraire, J, Vidal, F, Mayayo, E, et al. Gastric toxoplasmosis in the acquired immunodeficiency syndrome. Am J Gastroenterol. 1993;88:1464–5.Google Scholar
Merzianu, M, Gorelick, SM, Paje, V, et al. Gastric toxoplasmosis as the presentation of acquired immunodeficiency syndrome. Arch Pathol Lab Med. 2005;129:e8790.CrossRefGoogle ScholarPubMed
Oberhuber, G, Stolte, M. Giardiasis: analysis of histological changes in biopsy specimens of 80 patients. J Clin Pathol. 1990;43:641–3.Google Scholar
Bhansali, SK. Abdominal tuberculosis: experience with 300 cases. Am J Gastroenterol. 1977;67:324–37.Google Scholar
Atten, MJ, Attar, BM, Teopengco, E, et al. Gastric syphilis: a disease with multiple manifestations. Am J Gastroenterol. 1994;89:2227–9.Google Scholar
Mylona, EE, Baraboutis, IG, Papastamopoulos, V, et al. Gastric syphilis: a systematic review of published cases of the last 50 years. Sex Transm Dis. 2010;37:177–83.Google Scholar
Kaye, P, Abdulla, K, Wood, J, et al. Iron-induced mucosal pathology of the upper gastrointestinal tract: a common finding in patients on oral iron therapy. Histopathology. 2008;53:311–7.Google Scholar
Marginean, EC, Bennick, M, Cyczk, J, et al. Gastric siderosis: patterns and significance. Am J Surg Pathol. 2006;30:514–20.Google Scholar
Matsukuma, K, Gui, D, Olson, KA, et al. OsmoPrep-associated gastritis: a histopathologic mimic of iron pill gastritis and mucosal calcinosis. Am J Surg Pathol. 2016;40:1550–6.Google Scholar
Rashid, A, Hamilton, SR. Necrosis of the gastrointestinal tract in uremic patients as a result of sodium polystyrene sulfonate (Kayexalate) in sorbitol: an underrecognized condition. Am J Surg Pathol. 1997;21:60–9.Google Scholar
Greenson, JK, Trinidad, SB, Pfeil, SA, et al. Gastric mucosal calcinosis: calcified aluminium phosphate deposits secondary to aluminium-containing antacids or sucralfate therapy in organ transplant patients. Am J Surg Pathol. 1993;17:4550.Google Scholar
Goto, K, Ogawa, K. Lanthanum deposition is frequently observed in the gastric mucosa of dialysis patients with lanthanum carbonate therapy: a clinicopathologic study of 13 cases, including 1 case of lanthanum granuloma in the colon and 2 nongranulomatous gastric cases. Int J Surg Pathol. 2016;24:8992.Google Scholar
El-Zimaity, HM, Genta, RM, Graham, DY. Histological features do not define NSAID-induced gastritis. Hum Pathol. 1996;27:1348–54.CrossRefGoogle Scholar
Sung, J, Russell, RI, Yeomans, N, et al. Non-steroidal anti-inflammatory drug toxicity in the upper gastrointestinal tract.J Gastroenterol Hepatol. 2000;15(Suppl):G5868.Google Scholar
Gupta, A, Zheng, L, Ramanujam, V, et al. Novel use of pharmacogenetic testing in the identification of CYP2C9 polymorphisms related to NSAID-induced gastropathy. Pain Med. 2015;16:866–9.Google Scholar
Affolter, K, Samowitz, W, Boynton, K, et al. Doxycycline-induced gastrointestinal injury. Hum Pathol. 2017;66:212–15.Google Scholar
Shih, AR, Lauwers, GY, Mattia, A, et al. Vascular injury characterizes doxycycline-induced upper gastrointestinal tract mucosal injury. Am J Surg Pathol. 2017;41:374–81.Google Scholar
Parfitt, JR, Jayakumar, S, Driman, DK. Mycophenolate mofetil-related gastrointestinal mucosal injury: variable injury patterns, including graft-versus-host disease-like changes. Am J Surg Pathol. 2008;32:1367–72.Google Scholar
Nguyen, T, Park, JY, Scudiere, JR, et al. Mycophenolic acid (CellCept and Myofortic) induced injury of the upper GI tract. Am J Surg Pathol. 2009;33:1355–63.Google Scholar
Coyne, JD, Campbell, F. Microscopic features associated with mycophenolate mofetil in gastric and colonic biopsies. Histopathology. 2012;61:993–7.Google Scholar
Muir, A, Surrey, L, Kriegermeier, A, et al. Severe eosinophilic gastroenteritis in a Crohn’s disease patient treated with infliximab and adalimumab. Am J Gastroenterol. 2016;111:437–8.Google Scholar
Gonzalez, RS, Salaria, SN, Bohannon, CD, et al. PD-1 inhibitor gastroenterocolitis: case series and appraisal of ‘immunomodulatory gastroenterocolitis’. Histopathology. 2017;70:558–67.Google Scholar
Bavi, P, Butler, M, Serra, S, et al. Immune modulator-induced changes in the gastrointestinal tract. Histopathology. 2017;71:495–7.Google Scholar
Kobayashi, M, Yamaguchi, O, Nagata, K, et al. Acute haemorrhagic gastritis after nivolumab treatment. Gastrointest Endosc. 2017;86:915–16.Google Scholar
Johncilla, M, Grover, S, Zhang, X, et al. Morphological spectrum of immune checkpoint inhibitor therapy associated gastritis. Histopathology. 2019, Nov 6. doi: 10.1111/his.14029. [Epub ahead of print].Google Scholar
Zhang, L, Xia, WJ, Zhang, ZS, et al. Growth hormone used to control intractable bleeding caused by radiation-induced gastritis. World J Gastroenterol. 2015;21:9453–6.Google Scholar
Shukuwa, K, Kume, K, Yamasaki, M, et al. Argon plasma coagulation therapy for a hemorrhagic radiation-induced gastritis in patient with pancreatic cancer. Intern Med. 2007;46:975–7.Google Scholar
Goldgraber, MB, Rubin, CE, Palmer, WL, et al. The early gastric response to irradiation: a serial biopsy study. Gastroenterology. 1954;27:120.Google Scholar
Berthrong, M, Fajardo, LF. Radiation injury in surgical pathology. Part II. Alimentary tract. Am J Surg Pathol. 1981;5:153–78.Google Scholar
Berthrong, M. Pathologic changes secondary to radiation. World J Surg. 1986;10:155–70.Google Scholar
Grover, N, Johnson, A. Aminocaproic acid used to control upper gastrointestinal bleeding in radiation gastritis. Dig Dis Sci. 1997;42:982–3.Google Scholar
Sun, B, Lapetino, SR, Diffalha, SAL, et al. Microvascular injury in persistent gastric ulcers after yttrium-90 microsphere radioembolisation for liver malignancies. Hum Pathol. 2016;50:1114.Google Scholar
Petras, RE, Hart, WR, Bukowski, RM. Gastric epithelial atypia associated with hepatic arterial infusion chemotherapy: its distinction from early gastric carcinoma. Cancer. 1985;56:745–50.Google Scholar
Poon, TL, Wong, KF, Chan, MY, et al. Upper gastrointestinal problems in inhalational ketamine abusers. J Dig Dis. 2010;11:106–10.Google Scholar
Feliciano, DV, Ojukwu, JC, Rozycki, GS, et al. The epidemic of cocaine-related juxtapyloric perforations: with a comment on the importance of testing for Helicobacter pylori. Ann Surg. 1999;229:801–4; discussion 804–6.Google Scholar

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