Spontaneous superior mesenteric artery dissection due to idiopathic large vessel vasculitis-report of a case and review of the literature

Natarajan Sekar MS, MNAMS, MCh (Vascular Surgery), DSc, FRCS (Glas) , Rohit Mehra MS, DrNB (Peripheral vascular Surgery), FACS , Prem Chand Gupta MS
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Abstract

Background

Spontaneous isolated superior mesenteric artery dissection (SISMAD) is defined as superior mesenteric artery (SMA) dissection without the presence of aortic dissection. SISMAD can be asymptomatic or present with acute abdominal pain. Diagnosis is usually by computed tomography angiography (CTA). The exact etiology of SISMAD is not known. Atherosclerosis, hypertension, and high convexity of SMA have been implicated in the development of SISMAD. The majority can be managed by conservative measures. Endovascular stenting is advised when medical management fails. Open surgery has a limited role in this condition. Nonspecific large vessel vasculitis can cause inflammation around the visceral aorta, celiac artery, and SMA, leading to dissection in these vessels. Recognizing mesenteric artery vasculitis as a potential cause of abdominal pain can be challenging. Usually, they show only elevated nonspecific inflammatory markers and no features of systemic vasculitis. Addition of steroids can help to resolve the inflammation and avoid unnecessary intervention.

Methods

We are reporting here of a successful conservative management of a 55-year-old male patient with SISMAD due to isolated large vessel vasculitis involving the SMA. He had no systemic vasculitis, and the CTA showed typical features of SMA vasculitis and dissection. In addition to traditional medical management, he was given an infusion of methyl prednisolone followed by oral steroids.

Results

He had complete relief of symptoms and was discharged after 5 days. Follow-up CTA showed flow in the true lumen though the true lumen showed stenosis.

Conclusions

Isolated mesenteric artery vasculitis without systemic involvement is rarely reported in the literature, which can be the cause for dissection not being recognized. Patients diagnosed with SISMAD should undergo routine checks for inflammatory markers and vasculitis. If the markers are high, steroids may be added to the conservative measures to reduce the inflammation, which can help in remodeling of the SMA and thereby improving the outcome. The majority of patients with SISMAD could be initially managed by medical treatment. Persistent pain and fear of missing the diagnosis of bowel ischemia have been the most important causes for early conversion to intervention. The addition of a short course of steroids, especially for those with elevated inflammatory markers, can help in early resolution of the inflammation with relief of pain. This would help to avoid unnecessary intervention.
特发性大血管炎所致自发性肠系膜上动脉夹层1例报告及文献复习
自发性孤立性肠系膜上动脉夹层(SISMAD)被定义为肠系膜上动脉(SMA)夹层,但不存在主动脉夹层。SISMAD可无症状或伴有急性腹痛。诊断通常通过计算机断层血管造影(CTA)。SISMAD的确切病因尚不清楚。动脉粥样硬化、高血压和SMA的高凸度与SISMAD的发展有关。大多数人可以通过保守措施来管理。当医疗管理失败时,建议血管内支架植入术。在这种情况下,开放手术的作用有限。非特异性大血管炎可引起内脏主动脉、腹腔动脉和SMA周围的炎症,导致这些血管剥离。认识到肠系膜动脉血管炎是腹痛的潜在原因是具有挑战性的。通常,它们仅表现为非特异性炎症标志物升高,而无全身性血管炎的特征。添加类固醇可以帮助消除炎症,避免不必要的干预。方法:我们在此报告一例55岁男性患者,因孤立性大血管炎累及SMA,成功地进行了保守治疗。无全身性血管炎,CTA显示典型的SMA血管炎及夹层特征。除了传统的医疗管理外,他被给予甲基强的松龙输注,然后口服类固醇。结果患者症状完全缓解,5天后出院。随访CTA显示真管腔有血流,但真管腔狭窄。结论单纯性肠系膜动脉血管炎不累及全身的病例在文献中很少报道,这可能是未被识别的解剖原因。被诊断为SISMAD的患者应接受炎症标志物和血管炎的常规检查。如果标记物较高,可以在保守治疗中加入类固醇以减少炎症,这有助于SMA的重塑,从而改善预后。大多数SISMAD患者最初可以通过药物治疗来控制。持续的疼痛和害怕错过肠缺血的诊断是早期转向干预的最重要原因。添加短期类固醇治疗,特别是对于那些炎症标志物升高的患者,可以帮助早期解决炎症并减轻疼痛。这将有助于避免不必要的干预。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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