胃丛状纤维黏液瘤的诊疗进展
Clinical Treatment and Research Progress of Gastric Plexiform Angiomyxoid Myofibroblastic Tumor
DOI: 10.12677/ACM.2023.13102260, PDF,    科研立项经费支持
作者: 来志浩, 刘 奎, 李 坤, 曲林林*：青岛大学附属医院西海岸院区肝胆胰外科，山东 青岛
关键词: 胃丛状纤维黏液瘤；胃肿瘤；研究进展；Plexiform Angiomyxoid Myofibroblastic Tumor； Gastric Tumor； Research Progress
摘要: 胃丛状纤维黏液瘤是一种来源于胃肠间叶细胞的特殊类型肿瘤。该病临床上较罕见，具有独特的组织学特点和病理特征，但临床表现无显著特异性。由于胃丛状纤维黏液瘤的具体发病机制和疾病进展尚不十分明确，临床诊断易于漏诊或误诊。本文复习国内外文献对胃丛状纤维黏液瘤的流行病学特征、发病机制、临床表现、鉴别诊断、病理、免疫组化及治疗等方面进行系统综述，以期提高对胃丛状纤维粘液瘤的认识，为临床提供参考。
Abstract: Plexiform angiomyxoid myofibroblastic tumor (PAMT) was a specific type of tumor deriving from gastrointestinal mesenchymal cells. It was a rare disease with unique histological and pathological features. However, the clinical manifestation was non-specific. Because of the unclear pathogenesis and progression of PAMT, it prones to misdiagnosis. The epidemiological characteristics, pathogen-esis, clinical manifestations, differential diagnosis, pathological immunohistochemistry and treat-ment of PAMT were reviewed after studying domestic and foreign literatures. This article could im-prove the understanding of PAMT and provide clinical reference.
文章引用：来志浩, 刘奎, 李坤, 曲林林. 胃丛状纤维黏液瘤的诊疗进展[J]. 临床医学进展, 2023, 13(10): 16163-16168. https://doi.org/10.12677/ACM.2023.13102260

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