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首页> 外文期刊>Journal of Medical Case Reports >Chronic periaortitis (retroperitoneal fibrosis) concurrent with giant cell arteritis: a case report
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Chronic periaortitis (retroperitoneal fibrosis) concurrent with giant cell arteritis: a case report

机译:慢性腹膜炎(腹膜纤维化)并发巨细胞性动脉炎:一例报告

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Introduction Giant cell arteritis is the most common form of large-vessel vasculitides. However, it is probable that extracranial involvement is underdiagnosed in patients with classical giant cell arteritis. In the recent literature most cases of giant cell arteritis have been described in conjunction with aortic aneurysms or dissections. Nonetheless the coexistence of giant cell arteritis and retroperitoneal fibrosis is extremely rare. Here, we describe a case of giant cell arteritis at a very early clinical stage, in a woman with coexistence of retroperitoneal fibrosis. Case presentation We report a case of giant cell arteritis at a very early clinical stage, in a 47-year-old Greek woman with coexistence of retroperitoneal fibrosis who was admitted to our hospital with a history of high-grade fever and mild right periumbilical abdominal pain for the past 30 days. In the context of fever of unknown origin, an abdomen computed tomography was ordered. A temporal artery biopsy was also performed because during hospitalization she complained of a headache. Examination of eosin and hematoxylin slides from biopsy specimens of her temporal artery, showed lesions consisting of predominantly lymphocytes, few plasma cells and occasional polymorphonuclear leucocytes. In addition no giant cells were detected in examining biopsies at multiple levels. This was consistent with giant cell arteritis according to the American college of Rheumatology criteria. An abdomen computed tomography revealed the presence of a retroperitoneal soft-tissue mass located anteriorly to the upper infrarenal aorta at the site of the scintigraphic uptake. The computed tomography and magnetic resonance imaging characteristics of the mass were consistent with retroperitoneal fibrosis, and its morphology suggestive of benignity. Our patient started oral prednisolone and was afebrile from day one. Conclusions In our experience this is the first case of retroperitoneal fibrosis due to giant cell arteritis occurring at the same time. Involvement of the aorta (aortitis) and its branches has been also observed in a subset of patients with giant cell arteritis. In addition, giant cell arteritis has been associated with a markedly increased risk of aortic aneurysm particularly thoracic aortic aneurysm.
机译:简介巨细胞动脉炎是大血管血管炎的最常见形式。但是,经典巨细胞动脉炎患者颅外受累的可能性很低。在最近的文献中,已经描述了大多数的巨细胞动脉炎与主动脉瘤或夹层结合的情况。但是,巨细胞性动脉炎和腹膜后纤维化并存的情况极为罕见。在这里,我们描述了一个非常早期的临床阶段,伴有腹膜后纤维化的女性巨细胞性动脉炎。病例介绍我们报告了一个非常早期的临床阶段巨细胞性动脉炎的病例,该病例为一名47岁的希腊妇女,并存腹膜后纤维化,该患者曾入院并有高烧和轻度右胆管腹膜病史过去30天的疼痛。对于不明原因的发烧,需要进行腹部计算机断层扫描。还进行了颞动脉活检,因为在住院期间她抱怨头痛。从她的颞动脉活检标本中检查曙红和苏木素玻片,发现病变主要由淋巴细胞,少量浆细胞和偶发的多形核白细胞组成。另外,在多个水平的活检中未检测到巨细胞。根据美国风湿病学会的标准,这与巨细胞动脉炎是一致的。腹部计算机断层扫描显示在闪烁显像摄取部位位于腹膜下主动脉前方的腹膜后软组织肿块。肿物的计算机断层扫描和核磁共振成像特征与腹膜后纤维化一致,其形态提示良性。我们的患者开始口服泼尼松龙,从第一天开始发热。结论根据我们的经验,这是由于同时发生巨细胞动脉炎而引起的腹膜后纤维化的首例病例。在部分巨细胞性动脉炎患者中也观察到主动脉(主动脉炎)及其分支受累。另外,巨细胞动脉炎与主动脉瘤特别是胸主动脉瘤的风险显着增加有关。

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