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深静脉血栓形成的狰狞面目:股青肿——病例报告

The ugly face of deep vein thrombosis: Phlegmasia Cerulea Dolens-Case report.

作者信息

ELsaid Ayman S, AlQattan Abdullah Saleh, Elashaal Ehab, AlSadery Humood, AlGhanmi Ibrahim, Aldhafery Bander Fuhaid

机构信息

Department of General Surgery King Fahad University Hospital, Imam Abdulrahman Bin Faisal University, Saudi Arabia.

Medical Intern, King Fahad University Hospital, Imam Abdulrahman Bin Faisal University, Saudi Arabia.

出版信息

Int J Surg Case Rep. 2019;59:107-110. doi: 10.1016/j.ijscr.2019.05.021. Epub 2019 May 11.

Abstract

INTRODUCTION

Phlegmasia Cerulea Dolens (PCD), a rare & life-threatening condition caused by a massive deep venous thrombosis that is associated with arterial occlusion caused by the subsequent compartment syndrome.

CASE PRESENTATION

A 56-year-old male was diagnosed as a case of extensive left femoral DVT & pulmonary embolism. Two days after being managed by systemic thrombolytics & heparin, his condition worsened as he developed cyanosis of the affected limb, compartment syndrome & foot drop so he was referred to our facility for further management. CT venogram showed a thrombosis of the left popliteal vein extending into the left common iliac vein confirming the diagnosis of PCD & May-Turner syndrome. We adopted a limb preserving approach using a pharmacomechanical catheter directed thrombolysis (PCDT). The patient recovered fully with a complete resolution of his foot drop.

DISCUSSION

Several treatment options have been suggested to improve the outcomes of PCD, but due to the rarity of this condition a gold standard treatment is still controversial. But regardless of the chosen approach, there is an urgent need to decrease the thrombus burden to prevent further adverse sequelae like amputation or even death which can be achieved by using PCDT as it was demonstrated in our case.

CONCLUSION

Our case shows that a rare entity of DVT as PCD could be a result of improper management of acute proximal DVT in the background of anatomical variabilities & that despite the late presentation of such a rare condition there still a role for a limb preserving approach with endovascular techniques.

摘要

引言

股青肿(PCD)是一种罕见且危及生命的疾病,由大量深静脉血栓形成引起,并伴有随后的骨筋膜室综合征导致的动脉闭塞。

病例介绍

一名56岁男性被诊断为广泛的左股深静脉血栓形成和肺栓塞。在接受全身溶栓和肝素治疗两天后,他的病情恶化,出现患肢发绀、骨筋膜室综合征和足下垂,因此被转诊至我院进一步治疗。CT静脉造影显示左腘静脉血栓形成并延伸至左髂总静脉,确诊为PCD和May-Turner综合征。我们采用了一种保留肢体的方法,即使用药物机械导管直接溶栓(PCDT)。患者完全康复,足下垂完全消失。

讨论

已经提出了几种治疗方案来改善PCD的治疗效果,但由于这种疾病的罕见性,金标准治疗方案仍存在争议。但无论选择何种方法,迫切需要减轻血栓负荷以防止进一步的不良后果,如截肢甚至死亡,正如我们的病例所示,使用PCDT可以实现这一点。

结论

我们的病例表明,作为PCD的罕见深静脉血栓形成实体可能是在解剖变异背景下急性近端深静脉血栓形成管理不当的结果,并且尽管这种罕见疾病出现较晚,但血管内技术保留肢体的方法仍有作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/751f/6535643/241b0017aa98/gr1.jpg

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