系统性红斑狼疮急性腹痛的临床特征、影像学检查结果和预后:比较肠系膜血管炎、非肠系膜血管炎和手术条件。

IF 2.9 3区 医学 Q2 RHEUMATOLOGY Clinical Rheumatology Pub Date : 2024-10-18 DOI:10.1007/s10067-024-07189-8
Worawit Louthrenoo, Wanitcha Gumtorntip, Piyanut Thanunchai, Amonlaya Amantakul, Nuntana Kasitanon, Suwalee Pojchamarnwiputh
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引用次数: 0

摘要

目的确定系统性红斑狼疮(SLE)急性腹痛(AAP)患者的病谱、临床特征和预后:方法:对1987年1月至2023年6月期间狼疮队列中系统性红斑狼疮患者的医疗记录进行回顾。确定了需要住院治疗的急性腹痛患者,并将其分为三组:狼疮性肠系膜血管炎(LMV)、非LMV和手术性急性腹痛。每个 AAP 病例代表一名患者:在 1538 名患者中,有 62 人(4.03%)发生过 93 次 AAP。经排除后,31 名患者共发生了 39 次 LMV 事件,30 名患者共发生了 40 次非 LMV 事件(19 次是由于手术 AAP)。在 79 例 AAP 中,76 例(96.20%)为女性,平均(±SD)年龄和中位(IQR)病程分别为 36.76 ± 13.60 岁和 6(2,9)年。与非 LMV 组患者相比,LMV 组患者有更多的发热、恶心、呕吐和腹泻症状。他们还有更多的小肠受累、肠壁增厚、靶水增强征、肠系膜血管充血和肠系膜脂肪混浊,以及更高的系统性红斑狼疮疾病活动度。与手术 AAP 组相比,这些差异更为明显。使用皮质类固醇激素和免疫抑制剂治疗可为 LMV 组带来良好的治疗效果。40名非LMV AAP患者中有2名(5.00%)死亡,其中1名(5.26%)死于手术AAP组:结论:LMV在接受AAP治疗的系统性红斑狼疮患者中很常见。LMV通常表现为发热、胃肠道蠕动障碍症状、弥漫性腹痛以及活动性疾病的证据。局部腹痛并伴有腹膜征象的患者更倾向于接受手术治疗。要点 - 狼疮性肠系膜血管炎常见于伴有急性腹痛的系统性红斑狼疮患者。腹部计算机断层扫描发现的体征并不具有特异性,在其他原因引起的系统性红斑狼疮腹痛中也可观察到。对这些体征的解释应谨慎,并应结合病史采集和腹部体格检查结果 - 单用皮质类固醇激素或联合使用免疫抑制剂治疗狼疮肠系膜血管炎,通常会取得良好的疗效。
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Clinical features, imaging findings, and outcomes of acute abdominal pain in systemic lupus erythematosus: comparing mesenteric vasculitis, non-mesenteric vasculitis, and surgical conditions.

Objectives: To determine the spectrum, clinical features and outcomes in systemic lupus erythematosus (SLE) patients with acute abdominal pain (AAP).

Method: Medical records of SLE patients in a lupus cohort from January 1987 to June 2023 were reviewed. Patients with AAP requiring hospitalization were identified and categorized into 3 groups: lupus mesenteric vasculitis (LMV), non-LMV, and surgical AAP. Each AAP episode represented one patient.

Results: Of 1,538 patients in the cohort, 62 (4.03%) had 93 episodes of AAP. After exclusion, 31 patients had 39 LMV episodes, and 30 had 40 non-LMV episodes (19 due to surgical AAP). Seventy-six of the 79 AAP episodes (96.20%) were in females, with a mean ± SD age and median (IQR) disease duration of 36.76 ± 13.60 years and 6 (2, 9) years, respectively. Patients in the LMV group had more fever, nausea and vomiting, and diarrhea than those in the non-LMV group. They also had more small bowel involvement, bowel wall thickening, target water enhancement signs, mesenteric vessels engorgement and mesenteric fat cloudiness, and higher SLE disease activity. These differences were more pronounced when compared to the surgical AAP group. Treatment with corticosteroids and immunosuppressive drugs gave favorable outcomes in the LMV group. Two of 40 (5.00%) non-LMV AAP patients died, of which 1 (5.26%) was in the surgical AAP group.

Conclusion: LMV was common among SLE patients admitted for AAP. LMV usually presented with fever, gastrointestinal dysmotility symptoms, diffused abdominal pain, together with evidence of active disease. Localized abdominal pain with peritoneal signs favored surgical AAP. Key Points • Lupus mesenteric vasculitis is common among SLE patients presenting with acute abdominal pain. Its presence often associates with gastrointestinal symptoms together with other clinical manifestations of SLE • The signs in abdominal computed tomography findings are not specific and could be observed in other causes of abdominal pain in SLE. Interpretation of these signs should be cautionary and accompanied by history taking and physical abdominal findings • Treatment of lupus mesenteric vasculitis with corticosteroids alone, or in combination with immunosuppressive drugs, usually results in good outcomes.

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来源期刊
Clinical Rheumatology
Clinical Rheumatology 医学-风湿病学
CiteScore
6.90
自引率
2.90%
发文量
441
审稿时长
3 months
期刊介绍: Clinical Rheumatology is an international English-language journal devoted to publishing original clinical investigation and research in the general field of rheumatology with accent on clinical aspects at postgraduate level. The journal succeeds Acta Rheumatologica Belgica, originally founded in 1945 as the official journal of the Belgian Rheumatology Society. Clinical Rheumatology aims to cover all modern trends in clinical and experimental research as well as the management and evaluation of diagnostic and treatment procedures connected with the inflammatory, immunologic, metabolic, genetic and degenerative soft and hard connective tissue diseases.
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