梅-瑟纳综合征为白塞氏病的首发症状;一例罕见病例报告

Shorsh A. Mohammed, Fahmi H. Kakamad, Soran H. Tahir, Marwan N. Hassan, Miran Najmadden Hassan, Berun A. Abdalla, Dahat A. Hussein, Sasan M. Ahmed
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摘要

简介:梅-瑟纳综合征作为白塞病的表现症状在文献中是罕见的。本研究的目的是报告一例罕见的白塞氏病,其表现为梅-瑟纳综合征。病例报告:一名26岁女性,左腿疼痛持续一年。经检查,小腿有浅表静脉扩张和水肿。骨盆计算机断层扫描显示左侧髂总静脉明显狭窄,并被右侧髂总动脉压迫,提示May-Thurner综合征。在一段时间对药物没有反应后,她被转介到风湿病学家那里。病人被诊断为白塞氏病。她接受免疫抑制剂和糖皮质激素治疗。随访两个月后,病人的症状有所改善。结论:may - thurner综合征可能是白塞氏病的早期表现,可能使白塞氏病的临床表现进一步复杂化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
May-Thurner syndrome as the presenting symptom of Behcet’s disease; a rare case report
Introduction: May-Thurner syndrome as a presenting symptom of Behcet’s disease is rare in the literature. The aim of the current study is to report a rare case of Behcet's disease which has been presented with May-Thurner syndrome. Case report: A 26-year-old woman presented with left leg pain for a one-year duration. On examination, there were dilated superficial veins and edema in the calf. A computed tomography scan of the pelvis showed a markedly narrowed left common iliac vein which was compressed by the right common iliac artery, suggesting May-Thurner syndrome. After a period of not responding to medications, she had been referred to a rheumatologist. The patient was diagnosed with Behcet's disease. She received immunosuppressant agents and glucocorticoids. The patient's symptoms improved after two months of follow-up. Conclusion: May-Thurner syndrome could be an early manifestation of Behcet's disease, which may further complicate the clinical picture of Behcet's disease.
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