Minimally Invasive Surgical Approach in Granulomatosis with Polyangiitis Complicated with Intramural Descending Aorta Hematoma Followed by Aortic Wall Rupture.

IF 3.3 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Diagnostics Pub Date : 2025-01-09 DOI:10.3390/diagnostics15020144
Mihai-Lucian Ciobica, Alexandru-Sebastian Botezatu, Zoltan Galajda, Mara Carsote, Claudiu Nistor, Bianca-Andreea Sandulescu
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Abstract

Background and Clinical Significance: Granulomatosis with polyangiitis (GPA) represents a rare autoimmune disease with granulomatous inflammation, tissue necrosis, and systemic vasculitis of the small and medium blood vessels. Although the clinical elements vary, aortic involvement is exceptional and it represents a challenge that requires a rapid intervention with the potential of displaying a fulminant evolution. Case Presentation: We report a 64-year-old male with an 18-year history of GPA who presented atypical low back pain. Following ultrasound and computed tomography exams, the initial suspicion was an intramural descending aorta hematoma, surrounded by a peri-aortic sleeve suggesting a chronic inflammation. Serial non-invasive assessments revealed a progressive lesion within the next 10 to 12 days to an aortic wall rupture, despite the absence of previous aneurysmal changes. The peri-aortic fibrous inflammatory sleeve was life-saving, and emergency minimally invasive surgery was successful, including the massive improvement in back pain. Conclusions: To our knowledge, this is a very rare scenario in GPA; we found only 18 other cases (the oldest report being from 1994). An interventional approach was mentioned in a few cases as seen in this instance. Glucocorticoid medication for GPA might act as a potential contributor to symptomatic osteoporotic fractures which require a prompt differential diagnosis. Unusual aortic manifestations (such as intramural aortic hematoma or aortic wall rupture) are difficult to recognize since the index of clinical suspicion is rather low. A prompt intervention may be life-saving and a multidisciplinary team is mandatory. Minimally invasive surgical correction of the aortic event represents an optimum management in the modern era. Such cases add to the limited data we have so far with respect to unusual outcomes in long-standing GPAs.

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肉芽肿合并多血管炎合并降主动脉壁内血肿并发主动脉壁破裂的微创手术治疗。
背景与临床意义:肉芽肿病合并多血管炎(GPA)是一种罕见的自身免疫性疾病,以肉芽肿性炎症、组织坏死和中小血管全身性血管炎为主要表现。尽管临床因素各不相同,但主动脉受累是例外,它代表了一个挑战,需要快速干预,有可能显示暴发性演变。病例介绍:我们报告一位64岁男性,有18年的GPA病史,表现为非典型腰痛。经过超声和计算机断层检查,最初的怀疑是降主动脉壁内血肿,被主动脉周围套筒包围,提示慢性炎症。一系列非侵入性评估显示,尽管之前没有动脉瘤改变,但在接下来的10至12天内病变进展到主动脉壁破裂。主动脉周围纤维炎性套管挽救了生命,紧急微创手术取得了成功,背部疼痛得到了极大的改善。结论:据我们所知,这在GPA中是非常罕见的情况;我们只发现了其他18例(最早的报告是1994年的)。正如在本例中看到的那样,在一些情况下提到了介入方法。治疗GPA的糖皮质激素可能是导致骨质疏松性骨折的潜在因素,需要及时鉴别诊断。不寻常的主动脉表现(如主动脉壁内血肿或主动脉壁破裂)难以识别,临床怀疑指数较低。及时的干预可能挽救生命,一个多学科的团队是必要的。微创手术矫正主动脉事件代表了一个最佳的管理在现代时代。这些案例增加了我们迄今为止关于长期gpa不寻常结果的有限数据。
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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来源期刊
Diagnostics
Diagnostics Biochemistry, Genetics and Molecular Biology-Clinical Biochemistry
CiteScore
4.70
自引率
8.30%
发文量
2699
审稿时长
19.64 days
期刊介绍: Diagnostics (ISSN 2075-4418) is an international scholarly open access journal on medical diagnostics. It publishes original research articles, reviews, communications and short notes on the research and development of medical diagnostics. There is no restriction on the length of the papers. Our aim is to encourage scientists to publish their experimental and theoretical research in as much detail as possible. Full experimental and/or methodological details must be provided for research articles.
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