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[慢性主动脉周炎临床特征分析]

[Analysis of clinical features of chronic periaortitis].

作者信息

Tian Xin-ping, Bi Dan-yan, Zhang Feng-chun, Zeng Xiao-feng, Yu Meng-xue, Tang Fu-lin

机构信息

Department of Rheumatology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing 100730, China.

出版信息

Zhonghua Yi Xue Za Zhi. 2006 Apr 18;86(15):1035-9.

Abstract

OBJECTIVE

Understand the clinical features of chronic periaortitis.

METHODS

The medical records of 28 cases with definite diagnosis of chronic periaortitis were reviewed retrospectively.

RESULTS

Among these 28 cases, 20 (71.4%) fulfilled the diagnostic criteria of idiopathic retroperitoneal fibrosis (IPF), 5 (17.8%) were inflammatory abdominal aortic aneurysm (IAAA) and 3 (10.7%) were perianeurysmal retroperitoneal fibrosis (PARF). The common symptoms were abdominal blunt pain (35.7%), lumbago (25%), loss of body weight (25%), abdominal distension (17.8%) and lower extremities pitting edema (17.8%). Hydronephrosis was found by B ultrasonography in 17 (85%) patients with IPF. Dilated abdominal aorta were found in 7 patients. One case was complicated with ankylosing spondylitis and another one was diagnosed to have undifferentiated connective diseases. All 5 IAAA patients were treated by aneurysm segregation or stent implantation, but none had medical therapy. The 3 perianeurysmal retroperitoneal fibrosis patients were mis-diagnosed as with either IPF or AAA. Seventeen patients in this group were treated with corticosteroid combined with immunosuppressive agents or tamoxifen. Four cases were followed up and their conditions were improved which were demonstrated by repeated CT or MRI.

CONCLUSION

Chronic periaortitis is a rare autoimmune rheumatic disease. IPF is the most common one compared to IAAA and PARF. It can be complicated with autoimmune disorders or serum auto-antibodies. No case with other organ fibrosis disorder wis observed in this study. Radiological examination and pathological examination are necessary for confirming the diagnosis. Corticosteroid combined with immunosuppressive agents or tamoxifen is the effective treatment.

摘要

目的

了解慢性主动脉周炎的临床特征。

方法

回顾性分析28例确诊为慢性主动脉周炎患者的病历资料。

结果

28例患者中,20例(71.4%)符合特发性腹膜后纤维化(IPF)诊断标准,5例(17.8%)为炎性腹主动脉瘤(IAAA),3例(10.7%)为动脉瘤周围腹膜后纤维化(PARF)。常见症状为腹部钝痛(35.7%)、腰痛(25%)、体重减轻(25%)、腹胀(17.8%)和下肢凹陷性水肿(17.8%)。17例(85%)IPF患者经B超检查发现肾积水。7例患者发现腹主动脉扩张。1例合并强直性脊柱炎,另1例诊断为未分化结缔组织病。5例IAAA患者均接受动脉瘤分离或支架植入治疗,但均未接受药物治疗。3例动脉瘤周围腹膜后纤维化患者被误诊为IPF或AAA。该组17例患者接受了糖皮质激素联合免疫抑制剂或他莫昔芬治疗。4例患者接受随访,经重复CT或MRI检查显示病情改善。

结论

慢性主动脉周炎是一种罕见的自身免疫性风湿性疾病。与IAAA和PARF相比,IPF最为常见。它可合并自身免疫性疾病或血清自身抗体。本研究未观察到合并其他器官纤维化疾病的病例。确诊需要影像学检查和病理检查。糖皮质激素联合免疫抑制剂或他莫昔芬是有效的治疗方法。

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