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主动脉炎作为食管癌的先兆

Aortitis as a Harbinger of Esophageal Cancer.

作者信息

Ganchinho Lucas Sandra, Alfaiate Filipe, Santos Inês, Rocha Rita, Lino Ireneia

机构信息

Internal Medicine, Hospital do Espírito Santo de Évora E.P.E., Évora, PRT.

Cardiology, Hospital do Espírito Santo de Évora E.P.E., Évora, PRT.

出版信息

Cureus. 2021 Nov 30;13(11):e20065. doi: 10.7759/cureus.20065. eCollection 2021 Nov.

Abstract

Aortitis is a rare diagnosis that requires a high index of suspicion due to nonspecific symptoms and its multiplicity of etiologies. An 80-year-old man, independent in activities of daily living (ADLs), had three consecutive hospitalizations in three months for fever, general malaise, anorexia associated with arthritis of the hands and feet with the inability to walk. Inflammatory markers were increased without a focus of infection identified. Upper digestive endoscopy (UDE), colonoscopy, blood cultures, thoracoabdominal-pelvic CT and transthoracic (TT) echocardiogram were performed without changes, with discharge for consultation after demonstrating apyrexia. At the patient second hospitalization for fever and arthritis, a transesophageal echocardiogram was performed that showed the presence of multiple complex atherosclerotic plaques, with associated thrombi in all segments of the aorta with a suspicious mass of vegetation on the aorta. Thoracic-abdominopelvic CT demonstrated calcified atheromatosis of the entire aorta with para-aortic nodes; MRI showed aortic thickening; and autoimmunity study was negative. Aortitis was the working diagnosis of possible infectious etiology and anticoagulation and antibiotic therapy were started. Fever recurred and a third admission led to a working diagnosis of inflammatory, non-infectious aortitis. The patient responded well to empiric corticosteroids. The patient followed up in consultation, remained asymptomatic under a low dose of corticosteroids with negative temporal artery biopsy. In the sixth month, he repeated UDE due to dysphagia, which showed the presence of esophageal neoformation with the histological diagnosis of squamous cell carcinoma, maintaining on the CT as alterations in the aorta. This is an unusual case of aortitis associated with arthritis with improvement after corticosteroids, which interestingly occurred before the progression of esophageal cancer. In hindsight, we think this may have been a large vessel paraneoplastic vasculitis that preceded the detection of esophageal squamous cell carcinoma.

摘要

主动脉炎是一种罕见的诊断,由于其症状不具特异性且病因多样,因此需要高度怀疑。一名80岁、日常生活活动(ADL)自理的男性,在三个月内连续三次因发热、全身不适、厌食伴手足关节炎且无法行走而住院。炎症指标升高,但未发现感染病灶。进行了上消化道内镜检查(UDE)、结肠镜检查、血培养、胸腹盆腔CT和经胸(TT)超声心动图检查,均无异常发现,退热后出院进行会诊。在患者因发热和关节炎第二次住院时,进行了经食管超声心动图检查,结果显示存在多个复杂的动脉粥样硬化斑块,主动脉各段均伴有血栓,主动脉上有可疑的赘生物团块。胸腹盆腔CT显示整个主动脉有钙化性动脉粥样硬化伴主动脉旁淋巴结肿大;MRI显示主动脉增厚;自身免疫研究为阴性。初步诊断为可能由感染引起的主动脉炎,并开始进行抗凝和抗生素治疗。发热复发,第三次入院后初步诊断为炎症性、非感染性主动脉炎。患者对经验性使用的皮质类固醇反应良好。患者在会诊后进行随访,在低剂量皮质类固醇治疗下无症状,颞动脉活检为阴性。在第六个月时,患者因吞咽困难再次进行UDE检查,结果显示存在食管新生物,组织学诊断为鳞状细胞癌,CT显示主动脉仍有改变。这是一例罕见的主动脉炎合并关节炎病例,在皮质类固醇治疗后病情改善,有趣的是这发生在食管癌进展之前。事后看来,我们认为这可能是一种在食管鳞状细胞癌被发现之前就已存在的大血管副肿瘤性血管炎。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/430d/8718965/d2689d3d036a/cureus-0013-00000020065-i01.jpg

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