Mills Ch22 Stomach

613

CHAPTER 22:  Stomach

IM also shows changes in mucin core peptide expres- sion. Normally, the gastric surface epithelium expresses MUC5AC and smaller amounts of MUC1. In complete IM of the stomach, this expression is lost and the goblet cells stain for intestinal mucin (MUC2). Incomplete metaplasia may express mixtures of all types of mucin core peptides. There are also differences in mucin core protein expression between gastric cardiac metaplasia and Barrett metaplasia, but these are inconsistent and not particularly helpful for diagnostic purposes (26). Minor degrees of gastric IM are relatively common in persons in North America and elsewhere. The variants described above rarely exist as a pure entity, and mixtures of the various types within the same gastric foveola are encountered frequently. However, IM should never be con- sidered normal and almost always reflects some degree of gastric damage, usually from chronic gastritis. Less commonly encountered forms of metaplasia include subnuclear vacuolation (38) and ciliated meta- plasia (39). These changes all involve the pyloric mucus glands. Subnuclear vacuolation is not strictly a metaplas- tic change because it does not simulate the appearance of any other type of normal cells and probably represents a degenerative change secondary to gastritis or duodenal reflux. The vacuoles are clear on H&E sections and indent the nucleus. Ultrastructurally, they consist of a membrane- lined space derived either from endoplasmic reticulum or Golgi and probably contain nonglycoconjugated mucus core protein (40). Ciliated cells are found at the base of antral glands where there is superficial IM (37). The cause and significance of this change is not known. Pancreatic acinar metaplasia (41) may be present in up to 1.2% of gastric biopsy samples or 13% of gastrectomy speci- mens. The cells, which are indistinguishable from normal acinar cells, also produce lipase and trypsinogen. Seventy- five percent of cases are positive for amylase. Cells are pres- ent in nests and variably sized lobules scattered among the cardiac and oxyntic mucosae. Islets are not present. SPECIMEN HANDLING Gastric mucosa is delicate and should be handled with care. Tissue should be gently removed from the biopsy for- ceps and oriented before being placed flat on a supportive mesh, such as filter paper or Gelfoam. A variety of fixatives are suitable, depending on personal preferences, although routine formalin is suitable for most purposes. Sections are cut in ribbons, usually at two or three levels. For the best results, it is suggested that gastrectomy specimens be opened and pinned out on a corkboard or wax platform before being immersed in formalin and fixed overnight. If sections are taken directly from a fresh speci- men, they almost invariably curl up, resulting in irregular orientation of the final slide.

REFERENCES 1. Lewin KJ, Riddell RH, Weinstein WM. Normal structure of the stomach. In: Lewin KJ, Riddell RH, Weinstein WM, eds. Gastrointestinal Pathology and its Clinical Implications . New York: Igaku-Shoin; 1992:496–505. 2. Jacobson BC, Crawford JM, Farraye FA. GI tract endoscopic and tissue processing techniques and normal histology. In: Odze RD, Goldblum JR, eds. Surgical Pathology of the GI Tract Liver and Pancreas . 2nd ed. Philadelphia, PA: WB Saunders; 2009:3–30. 3. Mackintosh CE, Kreel L. Anatomy and radiology of the areae gastricae. Gut 1977;18:855–864. 4. Piasecki C. Blood supply to the human gastroduodenal mucosa with special reference to the ulcer-bearing areas. J Anat 1974;118(Pt 2):295–335. 5. Lehnert T, Erlandson RA, Decosse JJ. Lymph and blood cap- illaries in the human gastric mucosa. A morphologic basis for metastasisinearlygastriccarcinoma. Gastroenterology 1985;89: 939–950. 6. Listrom MB, Fenoglio-Preiser CM. Lymphatic distribution of the stomach in normal, inflammatory, hyperplastic, and neoplastic tissue. Gastroenterology 1987;93:506–514. 7. Schmidt B, Yoon SS. D1 versus D2 lymphadenectomy for gastric cancer. J Surg Oncol 2013;107:259–264. 8. Ajani JA, In H, Sano T, et al. Stomach. In: Amin M, ed. AJCC Cancer Staging Manual . 8th ed. Chicago, IL: American Joint Committee on Cancer; 2017:259–264. 9. Filipe MI. Mucins in the human gastrointestinal epithelium: A review. Invest Cell Pathol 1979;2:195–216. 10. Chandrasoma PT, Der R, Ma Y, et al. Histology of the gas- troesophageal junction: An autopsy study. Am J Surg Pathol 2000;24:402–409. 11. Sarbia M, Donner A, Gabbert HE. Histopathology of the gas- troesophageal junction: A study on 36 operation specimens. Am J Surg Pathol 2002;26:1207–1212. 12. Kilgore SP, Ormsby AH, Gramlich TL, et al. The gastric cardia: Fact or fiction? Am J Gastroenterol 2000;95:921–924. 13. Zhou H, Greco MA, Daum F, et al. Origin of cardiac mucosa: Ontogenic consideration. Pediatr Dev Pathol 2001;4:358–363. 14. Glickman JN, Chen YY, Wang HH, et al. Phenotypic charac- teristics of a distinctive multilayered epithelium suggests that it is a precursor in the development of Barrett’s esophagus. Am J Surg Pathol 2001;25:569–578. 15. Lash RH, Lauwers G, Odze RD, et al. Inflammatory disorders of the stomach. In: Odze RD, Goldblum JR, eds. Surgical Pathology of the GI Tract, Liver, Biliary Tract and Pancreas . 2nd ed. Philadelphia, PA: WB Saunders; 2009:269–320. 16. Goldblum JR. Inflammation and intestinal metaplasia of the gastric cardia: Helicobacter pylori, gastroesophageal reflux disease or both. Dig Dis 2000;18:14–19. 17. Goldman H, Ming SC. Mucins in normal and neoplastic gastrointestinal epithelium. Histochemical distribution. Arch Pathol 1968;85:580–586. 18. Matsuyama M, Suzuki H. Differentiation of immature mucous cells into parietal, argyrophil, and chief cells in stomach grafts. Science 1970;169:385–387. 19. Grimelius L. A silver stain for alpha-2 cells in human pancreatic islets. Acta Soc Med Ups 1968;73:243–270.

Made with FlippingBook - Online catalogs