Hu Xiao-Tong, Wang Dong
Department of Health Management, Daping Hospital, Army Medical University, Chongqing, China.
Department of Gastroenterology, The Ninth People'S Hospital of Chongqing, No. 69, Jialing Village, Beibei District, Chongqing, China.
Eur J Med Res. 2025 Apr 1;30(1):219. doi: 10.1186/s40001-025-02505-7.
Idiopathic mesenteric phlebosclerosis (IMP) is a rare form of ischemic colitis that predominantly impacts Asian populations. Despite some recognizable signs, there is a significant lack of awareness about IMP. In this review, we explore the etiology, pathogenesis, imaging manifestations, endoscopic traits, and therapeutic modalities of IMP. In addition, we discuss the deficiencies in the current comprehension of IMP and the potential research orientations in future.
特发性肠系膜静脉硬化（IMP）是一种罕见的缺血性结肠炎形式，主要影响亚洲人群。尽管有一些可识别的体征，但人们对IMP的认识仍严重不足。在本综述中，我们探讨了IMP的病因、发病机制、影像学表现、内镜特征和治疗方式。此外，我们还讨论了目前对IMP认识的不足之处以及未来潜在的研究方向。
