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新形成的海绵状血管瘤在血栓形成的发育性静脉异常中的磁共振演变:一例报告。

Magnetic resonance evolution of de novo formation of a cavernoma in a thrombosed developmental venous anomaly: a case report.

机构信息

†Division of Neuroradiology, Department of Medical Imaging, Toronto Western Hospital, University Health Network, Toronto, Ontario, Canada; ‡Division of Neurosurgery, Department of Surgery, Taipei Cathay General Hospital, Taipei, Taiwan.

出版信息

Neurosurgery. 2013 Oct;73(4):E739-44; discussion E745. doi: 10.1227/NEU.0000000000000002.

Abstract

BACKGROUND AND IMPORTANCE

Mechanisms that lead to de novo formations of nonfamilial-type cavernomas are not well understood. One of the interesting hypotheses is the causative relationship between developmental venous anomaly (DVA) and cavernoma formation. We report a unique case in which serial imaging demonstrated the evolution of de novo formation of a cavernoma in association with a thrombosed DVA. A detailed review of the causal hypothesis between a DVA and cavernoma is also provided.

CLINICAL PRESENTATION

We report a 37-year-old female patient in whom a cavernoma-like lesion arose 1 year after the progressive thrombosis of a medullary (or caput medusa) vein of a DVA. The presence of an acute angulation in the draining vein may have prompted an intrinsic outflow restriction. Possible worsening of venous disequilibrium led to subsequent thrombus progression, venous congestion, and occlusion of the vein with venous dilation and signs of stasis on follow-up magnetic resonance imaging. Finally, this developed into a lobulated lesion with salt-and-pepper appearance at the converging region of medullary tributaries, which typified the classic features of a cavernoma.

CONCLUSION

Compared with other published cases of de novo cavernoma formation in relation to a DVA, our case, for the first time, allows us to witness the temporal evolution from a thrombosed DVA to the birth of a cavernoma around it. This supports the hypothesis that the cavernoma can be an acquired disease that arises from a DVA.

摘要

背景与重要性

导致非家族性海绵状血管瘤新形成的机制尚不清楚。其中一个有趣的假设是发育性静脉异常(DVA)与海绵状血管瘤形成之间的因果关系。我们报告了一个独特的病例,其中连续影像学显示在血栓形成的 DVA 旁发生新形成的海绵状血管瘤。还对 DVA 和海绵状血管瘤之间的因果假说进行了详细的回顾。

临床表现

我们报告了一名 37 岁女性患者,在 DVA 的髓内(或水母头)静脉进行性血栓形成 1 年后,出现了海绵状病变。引流静脉中的急性成角可能导致了内在的流出受限。可能静脉平衡恶化导致随后的血栓进展、静脉充血以及静脉扩张和淤滞征象的闭塞,在随访磁共振成像上可见。最终,这发展为具有分叶状外观的病变,在髓质支流汇聚区呈椒盐状外观,典型的海绵状血管瘤的特征。

结论

与 DVA 相关的其他已发表的新形成海绵状血管瘤病例相比,我们的病例首次使我们能够见证从血栓形成的 DVA 到其周围出现海绵状血管瘤的时间演变。这支持了海绵状血管瘤是一种获得性疾病,起源于 DVA 的假说。

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