Geriatric Center, Zhengzhou Ninth People's Hospital, 25 Sha Kou Road, 450008, Zhengzhou, Henan, China.
Radiology, Zhengzhou Ninth People's Hospital, 25 Sha Kou Road, 450008, Zhengzhou, Henan, China.
BMC Gastroenterol. 2024 Jan 24;24(1):48. doi: 10.1186/s12876-024-03136-8.
Mesenteric panniculitis (MP) represents the uncommon, benign and chronic inflammatory disorder affecting the mesenteric adipose tissues. Its etiology, diagnosis and treatment remain unnoticed. Our report focused on shedding more lights on this condition.
Seventeen MP patients were identified by searching the electronic medical record system in the Zhengzhou Ninth People's Hospital using the search terms "Mesenteric panniculitis" from October 2015 to March 2023. All cases were diagnosed with MP through computed tomography (CT). Their clinical features and treatments were analyzed.
There were altogether 17 cases enrolled for this analysis. The male to female ratio was 8:9, and the median age at diagnosis was 64 (range: 37-96) years. There were 15 patients (88.2%) showing abdominal pain to varying degrees. The proportions of symptoms of nausea, vomiting and fever were 23.5%, 23.5% and 41.2%, respectively. Neoplastic disease was present in 3 patients (17.6%). Meanwhile, 9 patients (52.9%) had gallstones, 3 (17.6%) had cholecystitis and 1 (5.9%) had gallbladder polyps. Six patients (35.3%) received antibiotics treatment only and 1 (5.9%) received oral antibiotics and prednisone. One patient (5.9%) received antibiotics followed by prednisone treatment, because the symptoms were significantly relieved after antibiotic treatment, while the disease recurred soon after, and the symptoms improved again after prednisone treatment. The abdominal pain in 9 patients (52.9%) was relieved spontaneously. Two patients (11.8%) died, including one due to respiratory failure caused by pneumonia and the other one because of pancreatic cancer with lung and liver metastases.
MP is a poorly understood chronic inflammatory disease. Patients often have abdominal pain as the main symptom, accompanied by comorbidities in the gallbladder, and the prognosis is usually good after correct diagnosis and treatment, Therefore, the present report aims to promote the awareness among clinicians of patients with non-classic abdominal symptoms, so as to avoid misdiagnosis or missed diagnosis.
肠系膜脂膜炎(MP)是一种罕见的、良性的、慢性炎症性疾病,影响肠系膜脂肪组织。其病因、诊断和治疗仍未被重视。我们的报告旨在进一步阐明这种疾病。
2015 年 10 月至 2023 年 3 月,通过在郑州九院电子病历系统中使用“肠系膜脂膜炎”检索词,搜索了 17 例 MP 患者。所有病例均通过计算机断层扫描(CT)诊断为 MP。分析了他们的临床特征和治疗方法。
本分析共纳入 17 例患者。男女比例为 8:9,中位诊断年龄为 64 岁(范围:37-96 岁)。15 例(88.2%)患者有不同程度的腹痛。恶心、呕吐和发热的症状比例分别为 23.5%、23.5%和 41.2%。3 例(17.6%)患者患有肿瘤性疾病。同时,9 例(52.9%)患者有胆囊结石,3 例(17.6%)有胆囊炎,1 例(5.9%)有胆囊息肉。6 例(35.3%)患者仅接受抗生素治疗,1 例(5.9%)患者接受口服抗生素和泼尼松治疗。1 例(5.9%)患者先接受抗生素治疗,后接受泼尼松治疗,因为抗生素治疗后症状明显缓解,但疾病很快复发,泼尼松治疗后症状再次改善。9 例(52.9%)患者腹痛自发缓解。2 例(11.8%)患者死亡,1 例因肺炎导致呼吸衰竭,另 1 例因胰腺癌伴肺、肝转移。
MP 是一种尚未被充分认识的慢性炎症性疾病。患者常以腹痛为主要症状,伴有胆囊合并症,正确诊断和治疗后预后通常良好。因此,本报告旨在提高临床医生对非典型腹部症状患者的认识,避免误诊或漏诊。