Du Shuwen, Yang Shanbing, Jia Kangmei, Du Peng, Zhang Limin, Wang Jiheng
Department of Gastroenterology, The Seventh Medical Center, Chinese PLA General Hospital, No.5, Nanmengcang Hutong, Beijing, China.
Department of Colorectal Surgery, Xinhua Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
BMC Gastroenterol. 2021 Mar 22;21(1):133. doi: 10.1186/s12876-021-01702-y.
Fibromuscular dysplasia (FMD) is a type of unexplained nonatherosclerotic vascular disease that usually involves the renal and internal carotid arteries and rarely involves the mesenteric artery. Mesenteric artery FMD is difficult to distinguish from Crohn's disease (CD) and Behcet's disease (BD) solely based on symptoms. Patients with mesenteric artery FMD can present with an acute abdomen, but case reports of patients who have a long medical history and undergo multiple bowel resections are extremely rare.
The patient was a 45-year-old woman with an 11-year history of intermittent lower abdominal pain and fever. At the age of 34 years, she underwent right hemicolectomy and appendectomy due to an acute abdomen. She suffered from oral ulcers between 34 and 36 years old. A clinical diagnosis of presumed CD was made by the age of 41, and she was treated with mesalazine; however, the effect was poor. At the age of 42, she came to our centre, and based on her atypical symptoms and examination results, we thought she had CD. Hence, she was treated with glucocorticoids for 3 years. However, when she was 45, due to steroid dependence, thalidomide tablets were added. Unfortunately, she suffered from another episode of intestinal obstruction. Therefore, she underwent enterectomy. The postoperative histopathological diagnosis was mesenteric artery FMD. She no longer underwent pharmacotherapy after the surgery. Although she did not have any of her previous symptoms and postoperative colonoscopy showed no signs of recurrence, splenomegaly and abnormal routine blood results were still present.
Patients with mesenteric artery FMD can present with an acute abdomen. In addition, the symptoms and endoscopic manifestations of mesenteric artery FMD may appear similar to CD and BD. Hence, it is difficult to make a clear clinical diagnosis and proceed with treatment. Mesenteric artery FMD often requires surgical pathology to confirm its diagnosis. For patients who suffer from this disorder, surgery may be the best choice to improve the patient's quality of life.
纤维肌发育不良(FMD)是一种原因不明的非动脉粥样硬化性血管疾病,通常累及肾动脉和颈内动脉,很少累及肠系膜动脉。仅根据症状很难将肠系膜动脉FMD与克罗恩病(CD)和白塞病(BD)区分开来。肠系膜动脉FMD患者可出现急腹症,但有长期病史并接受多次肠切除术的患者病例报告极为罕见。
该患者为一名45岁女性,有11年间歇性下腹痛和发热病史。34岁时,因急腹症接受了右半结肠切除术和阑尾切除术。34至36岁期间她患有口腔溃疡。41岁时临床诊断为疑似CD,并接受美沙拉嗪治疗;然而,效果不佳。42岁时,她来到我们中心,根据其非典型症状和检查结果,我们认为她患有CD。因此,她接受了3年的糖皮质激素治疗。然而,45岁时,由于对类固醇依赖,加用了沙利度胺片。不幸的是,她又发生了一次肠梗阻。因此,她接受了肠切除术。术后组织病理学诊断为肠系膜动脉FMD。术后她不再接受药物治疗。尽管她没有了之前的任何症状,术后结肠镜检查也未显示复发迹象,但仍存在脾肿大和血常规异常。
肠系膜动脉FMD患者可出现急腹症。此外,肠系膜动脉FMD的症状和内镜表现可能与CD和BD相似。因此,很难做出明确的临床诊断并进行治疗。肠系膜动脉FMD通常需要手术病理来确诊。对于患有这种疾病的患者,手术可能是改善患者生活质量的最佳选择。