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Published on: June 2, 2015
The ugly face of deep vein thrombosis: Phlegmasia Cerulea Dolens-Case report
Ayman S ELsaid1, Abdullah Saleh AlQattan2, Ehab Elashaal1
1Department of General Surgery King Fahad University Hospital, Imam Abdulrahman Bin Faisal University, Saudi Arabia.
Insights
Phlegmasia Cerulea Dolens (PCD), a rare condition from deep venous thrombosis, can be treated with pharmacomechanical catheter-directed thrombolysis (PCDT). This limb-preserving approach successfully resolved symptoms in a patient with extensive thrombosis and May-Thurner syndrome.
Area of Science:
- Vascular Surgery
- Interventional Radiology
- Cardiology
Background:
- Phlegmasia Cerulea Dolens (PCD) is a rare, life-threatening condition resulting from extensive deep venous thrombosis (DVT) causing arterial occlusion and compartment syndrome.
- Prompt diagnosis and management are crucial to prevent limb loss and mortality.
Purpose of the Study:
- To present a case of PCD secondary to May-Thurner syndrome managed with a limb-preserving endovascular approach.
- To highlight the efficacy of pharmacomechanical catheter-directed thrombolysis (PCDT) in treating complex DVT cases.
Main Methods:
- A 56-year-old male with extensive left femoral DVT and pulmonary embolism presented with worsening cyanosis, compartment syndrome, and foot drop.
- CT venogram confirmed PCD and May-Thurner syndrome.
- Pharmacomechanical catheter-directed thrombolysis (PCDT) was employed as a limb-preserving strategy.
Main Results:
- The patient achieved a full recovery with complete resolution of his foot drop.
- PCDT effectively reduced the thrombus burden, preventing adverse sequelae.
Conclusions:
- PCD, even when presenting late, can be effectively managed with endovascular techniques like PCDT.
- This case underscores the importance of considering anatomical variations and optimizing DVT management to prevent catastrophic outcomes.
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.
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