Localized primary gastric amyloidosis: Three case reports

被引：7

作者：

Liu, Xue-Mei ^{[1
]}

Di, Lian-Jun ^{[1
]}

Zhu, Jia-Xing ^{[1
]}

Wu, Xing-Long ^{[2
]}

Li, Hong-Ping ^{[1
]}

Wu, Hui-Chao ^{[1
]}

Tuo, Bi-Guang ^{[1
]}

机构：

[1] Zunyi Med Univ, Affiliated Hosp, Dept Gastroenterol, 149 Dalian Rd, Zunyi 563003, Guizhou, Peoples R China

[2] Zunyi Med Univ, Affiliated Hosp, Dept Pathol, Zunyi 563003, Guizhou, Peoples R China

来源：

WORLD JOURNAL OF CLINICAL CASES | 2020年 / 8卷 / 19期

基金：

中国国家自然科学基金;

关键词：

Localized gastric amyloidosis; Mucosa-associated lymphoid tissue lymphoma; Different outcomes; Rare disease; A case series study; Case report; GASTROINTESTINAL-TRACT; STOMACH; DEPOSITION; TUMOR; WOMAN;

D O I：

10.12998/wjcc.v8.i19.4667

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

BACKGROUND Localized primary gastric amyloidosis is a rare disorder characterized by the extracellular deposition of insoluble fibrillary protein in the stomach and can mimic various diseases on endoscopic examination, including gastrointestinal stromal tumors, gastric cancer and ulcers. CASE SUMMARIES Here, we report a series of three cases of localized gastric amyloidosis mimicking gastric mucosa-associated lymphoid tissue (MALT) lymphoma on endoscopic examination that were evaluated over the past ten years in our hospital. The different detection times of this rare disease resulted in three completely different outcomes, indicating the strong importance of early detection, diagnosis and treatment. The difficulties encountered in making an accurate diagnosis and differential diagnosis are highlighted, and this report provides clinical experience for the diagnosis of localized primary gastric amyloidosis. CONCLUSION Localized gastric amyloidosis is a rare metabolic disease that resembles MALT lymphoma. Early detection, diagnosis and treatment of localized gastric amyloidosis result in an excellent prognosis.

引用

页码：4667 / 4675

页数：9

共 24 条

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