CD73 缺乏导致动脉钙化的影像学发现:病例研究

Pub Date : 2024-02-09 DOI:10.3941/jrcr.v17i12.5175
Aniruddh Mandalapu, Kathryn J Stevens
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引用次数: 0

摘要

一名 52 岁的男性在危地马拉徒步旅行后出现右膝疼痛。回国后,他因膝关节内侧疼痛接受了膝关节核磁共振成像检查,结果显示为内侧半月板撕裂。然而,核磁共振成像显示腘动脉有明显的迂曲和密集钙化,这在随后的X光片上得到了证实。之前的腹部和下肢 CT 检查显示,双侧股动脉和腘动脉存在严重的异位和动脉钙化,但主动脉和髂总动脉没有钙化。四肢的双能 CT 检查显示,腕部、手部、踝关节和足部均有广泛的关节周围软组织钙化,但无尿酸证据。查看电子病历后发现,该患者被诊断为 CD73 缺乏引起的动脉钙化(ACDC),这是一种罕见的遗传性疾病,表现为手腕和手部疼痛,小腿、大腿和臀部跛行,进而发展为慢性足部缺血,可能危及肢体。患者参加了美国国立卫生研究院的双磷酸盐和双抗血小板治疗试验,症状有所稳定。本病例讨论了这种罕见疾病的影像学检查结果、需要考虑的鉴别诊断以及目前的治疗方法。
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Imaging findings of arterial calcification due to deficiency of CD73: A case study
A 52-year-old male developed right knee pain after hiking in Guatemala. On his return he underwent a knee MRI for an indication of medial knee pain, which demonstrated a medial meniscal tear. However, the MRI demonstrated marked tortuosity and dense calcification of the popliteal artery, confirmed on subsequent radiographs. Review of previous CT studies of the abdomen and lower extremities showed severe ectasia and arterial calcification in the femoral and popliteal arteries bilaterally, but no calcifications in the aorta and common iliac arteries. Dual energy CT studies of the extremities demonstrated extensive periarticular soft tissue calcification throughout the wrists, hands, ankle and feet without evidence of uric acid. Review of the electronic medical records revealed a diagnosis of Arterial Calcification due to Deficiency of CD73 (ACDC), a rare genetic disorder presenting with debilitating pain in the wrists and hands, claudication of the calves, thighs and buttocks, progressing to chronic ischemia of the feet which may be limb-threatening. The patient was enrolled in an NIH trial of bisphosphonates and dual-antiplatelet therapy with stabilization of symptoms. This case discusses the imaging findings of this rare condition, differential diagnosis to consider, and current management.
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