Klymenko Valeriia, Varughese Reba, Woolley Katherine A, Wetherell Joseph M, Mopuru Haritha, Mensah Edward, Siddiqui Imran
Department of Medicine, St. Vincent's Medical Center, Bridgeport, CT, USA.
Case Rep Gastrointest Med. 2021 Feb 8;2021:6629424. doi: 10.1155/2021/6629424. eCollection 2021.
Sclerosing mesenteritis (SM) is a rare inflammatory condition with unknown etiology that affects the mesenteric adipose tissue. We present a case of a 49-year-old male with severe abdominal pain who underwent abdominal biopsy confirming the presence of adipose inflammation and necrosis. The diagnosis of SM was made, and the patient was treated with prednisone and tamoxifen. As this condition is rare, there are no standard guidelines for management. This case aims to outline a possible treatment plan.
硬化性肠系膜脂膜炎（SM）是一种病因不明的罕见炎症性疾病，可累及肠系膜脂肪组织。我们报告一例49岁男性，因严重腹痛接受腹部活检，证实存在脂肪炎症和坏死。诊断为SM，患者接受泼尼松和他莫昔芬治疗。由于这种疾病罕见，目前尚无标准的治疗指南。本病例旨在概述一种可能的治疗方案。
