食道过度收缩无嗜酸性粒细胞浸润的主要碱性蛋白沉积1例。

IF 1.5 Q4 GASTROENTEROLOGY & HEPATOLOGY
DEN open Pub Date : 2025-09-29 DOI:10.1002/deo2.70206
Tetsuya Tatsuta, Keinosuke Hizuka, Shigeharu Ueki, Masatoshi Kaizuka, Shinji Oota, Keisuke Hasui, Hidezumi Kikuchi, Hiroto Hiraga, Daisuke Chinda, Hirotake Sakuraba
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引用次数: 0

摘要

食道过度收缩是一种以食道体过度收缩为特征的运动障碍。某些食道过度收缩的病例表现为肌层嗜酸性粒细胞浸润;然而,其临床意义尚不清楚。在此,我们报告一例食道过度收缩伴嗜酸性粒细胞炎症的病例,尽管苏木精和伊红染色未见嗜酸性粒细胞浸润。75岁男性,主要因摄入肉类引起吞咽困难。食管胃十二指肠镜检查显示食管体蠕动异常,食管下括约肌功能正常。根据芝加哥分类4.0版,高分辨率测压证实食道过度收缩。尽管药物治疗,但症状仍然存在,患者接受了经口内窥镜肌切开术。内环肌层活检显示苏木精和伊红染色未见明显嗜酸性细胞浸润。然而,免疫荧光染色的主要碱性蛋白(MBP),细胞毒性的嗜酸性粒细胞颗粒蛋白,持续存在于组织中,显示斑片状沉积。相应的反染色显示细胞核被嗜酸性物质包围,表明MBP通过嗜酸性细胞溶解释放。本病例表明,即使在没有嗜酸性粒细胞的情况下,嗜酸性粒细胞颗粒蛋白的免疫染色也可能发现食管肌层的嗜酸性活性。虽然嗜酸性粒细胞炎症在食管过度收缩中的确切致病作用尚不清楚,但MBP沉积可能反映了局部免疫介导的过程,导致运动障碍。需要进一步的研究来确定这些发现在食管运动障碍中的患病率、机制和临床意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Major Basic Protein Deposition Without Eosinophilic Infiltration in Hypercontractile Esophagus: A Case Report

Major Basic Protein Deposition Without Eosinophilic Infiltration in Hypercontractile Esophagus: A Case Report

Hypercontractile esophagus is a motility disorder characterized by excessive contractions in the esophageal body. Certain cases of hypercontractile esophagus exhibit eosinophilic infiltration in the muscle layer; however, its clinical significance is unclear. Here, we report a case of hypercontractile esophagus with possible eosinophilic inflammation despite the absence of eosinophilic infiltration on hematoxylin and eosin staining. A 75-year-old man presented with dysphagia, primarily triggered by the ingestion of meat. Esophagogastroduodenoscopy showed abnormal peristalsis of the esophageal body, while the lower esophageal sphincter function remained normal. High-resolution manometry confirmed hypercontractile esophagus, according to the Chicago Classification version 4.0. As symptoms persisted despite medical treatment, the patient underwent peroral endoscopic myotomy. Biopsies obtained from the inner circular muscle layer revealed no notable eosinophilic infiltration on hematoxylin and eosin staining. However, immunofluorescence staining for major basic protein (MBP), a cytotoxic eosinophil granule protein that persists in tissues, showed patchy depositions. Corresponding counterstaining revealed collapsed nuclei surrounded by eosinophilic material, suggesting MBP release via eosinophil cytolysis. This case demonstrated that immunostaining for eosinophil granule proteins may uncover eosinophilic activity in the esophageal muscle layer, even in the absence of eosinophils. While the precise pathogenic role of eosinophilic inflammation in hypercontractile esophagus remains unclear, MBP deposition could reflect a localized immune-mediated process contributing to motility disturbance. Further investigation is needed to determine the prevalence, mechanisms, and clinical implications of these findings in esophageal motor disorders.

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