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一例与慢性粒单核细胞白血病相关的副肿瘤性主动脉炎罕见病例。

A Rare Case of Paraneoplastic Aortitis Associated with Chronic Myelomonocytic Leukemia.

作者信息

Sasinowska Sylwia, Traisak Pamela, McCormack Michael, Eid Hala

机构信息

Division of Rheumatology, Cooper University Hospital, Camden, NJ, USA.

Division of Hematology-Oncology, MD Anderson Cancer Center, Cooper University Hospital, Camden, NJ, USA.

出版信息

Case Rep Hematol. 2017;2017:3091973. doi: 10.1155/2017/3091973. Epub 2017 May 25.

Abstract

Aortitis is a broad term describing inflammation of the aorta. The most common causes of aortitis are the large-vessel vasculitides giant cell arteritis and Takayasu arteritis. Other etiologies include aortitis associated with other autoimmune disorders, infectious causes, and paraneoplastic and idiopathic cases. We describe a rare case of a large-vessel arteritis occurring in association with chronic myelomonocytic leukemia (CMML). A 68-year-old female with recent diagnosis of CMML presented to our office for evaluation of abnormal chest computed tomography (CT) that showed inflammation surrounding the entirety of thoracic and abdominal aorta, consistent with aortitis. In the absence of other evident causes of large-vessel vasculitis, we attributed this finding to a paraneoplastic autoimmune phenomenon and started treatment with systemic glucocorticoids. This rare case emphasizes the need to recognize autoimmune complications in CMML and treat the inflammation along with the primary malignancy promptly.

摘要

主动脉炎是一个宽泛的术语,用于描述主动脉的炎症。主动脉炎最常见的病因是大血管血管炎,即巨细胞动脉炎和高安动脉炎。其他病因包括与其他自身免疫性疾病相关的主动脉炎、感染性病因以及副肿瘤性和特发性病例。我们描述了一例与慢性粒单核细胞白血病(CMML)相关的罕见大血管动脉炎病例。一名近期诊断为CMML的68岁女性因胸部计算机断层扫描(CT)异常前来我们科室就诊,CT显示胸主动脉和腹主动脉全程周围有炎症,符合主动脉炎表现。在没有其他明显的大血管血管炎病因的情况下,我们将这一发现归因于副肿瘤性自身免疫现象,并开始使用全身性糖皮质激素进行治疗。这个罕见病例强调了在CMML中认识自身免疫并发症并及时治疗炎症和原发性恶性肿瘤的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1109/5463136/2ed0ae147712/CRIHEM2017-3091973.001.jpg

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