Robert Odze Pathology, LLC, Boston, Massachusetts, USA.
Department of Medicine, Center for Esophageal Diseases, Baylor University Medical Center and Center for Esophageal Research, Baylor Scott and White Research Institute, Dallas, Texas, USA.
Clin Transl Gastroenterol. 2021 Apr 27;12(5):e00346. doi: 10.14309/ctg.0000000000000346.
Whether cardiac mucosa at the esophagogastric junction is normal or metaplastic is controversial. Studies attempting to resolve this issue have been limited by the use of superficial pinch biopsies, abnormal esophagi resected typically because of cancer, or autopsy specimens in which tissue autolysis in the stomach obscures histologic findings.
We performed histologic and immunohistochemical studies of the freshly fixed esophagus and stomach resected from 7 heart-beating, deceased organ donors with no history of esophageal or gastric disease and with minimal or no histologic evidence of esophagitis and gastritis.
All subjects had cardiac mucosa, consisting of a mixture of mucous and oxyntic glands with surface foveolar epithelium, at the esophagogastric junction. All also had unique structures we termed compact mucous glands (CMG), which were histologically and immunohistochemically identical to the mucous glands of cardiac mucosa, under esophageal squamous epithelium and, hitherto undescribed, in uninflamed oxyntic mucosa throughout the gastric fundus.
These findings support cardiac mucosa as a normal anatomic structure and do not support the hypothesis that cardiac mucosa is always metaplastic. However, they do support our novel hypothesis that in the setting of reflux esophagitis, reflux-induced damage to squamous epithelium exposes underlying CMG (which are likely more resistant to acid-peptic damage than squamous epithelium), and proliferation of these CMG as part of a wound-healing process to repair the acid-peptic damage could result in their expansion to the mucosal surface to be recognized as cardiac mucosa of a columnar-lined esophagus.
胃食管交界处的心脏黏膜是正常还是化生一直存在争议。试图解决这一问题的研究受到了浅表夹取活检、因癌症而通常切除的异常食管或胃尸检标本的限制,这些标本中胃组织自溶会掩盖组织学发现。
我们对 7 例无食管或胃部疾病史、无明显食管炎和胃炎组织学证据的心跳骤停器官捐献者的新鲜固定食管和胃组织进行了组织学和免疫组织化学研究。
所有研究对象的食管胃交界处均有心脏黏膜,由混合的黏液腺和泌酸腺以及表面的微凹上皮组成。所有研究对象还都有我们称之为致密黏液腺(CMG)的独特结构,这些 CMG 在组织学和免疫组织化学上与心脏黏膜的黏液腺相同,位于食管鳞状上皮下,并且在胃底整个无炎症的泌酸黏膜中也存在此前未描述过的 CMG。
这些发现支持心脏黏膜是一种正常的解剖结构,不支持心脏黏膜总是化生的假说。然而,它们确实支持我们的新假说,即在反流性食管炎的情况下,反流引起的鳞状上皮损伤暴露了潜在的 CMG(与鳞状上皮相比,CMG 可能更能抵抗酸-胃蛋白酶损伤),这些 CMG 的增殖作为修复酸-胃蛋白酶损伤的愈合过程的一部分,可能导致它们扩展到黏膜表面,被识别为柱状上皮食管的心脏黏膜。