TY - JOUR
T1 - Pelvic deep venous thrombosis mimicking lower limb cellulitis in systemic lupus erythematosus-associated antiphospholipid syndrome
AU - Wang, Chrong Reen
AU - Lee, Cheng Han
N1 - Funding Information:
The authors are indebted to doctors and nurses of National Cheng Kung University Hospital for their help in diagnosis and management of reported patients in this study. The author(s) received no financial support for the research, authorship, and/or publication of this article.
Publisher Copyright:
© The Author(s) 2022.
PY - 2022/4
Y1 - 2022/4
N2 - Objectives: Systemic lupus erythematosus (SLE) associated with antiphospholipid syndrome (APS) is a complex clinical scenario with thromboembolic events, lupus activity, and related therapeutic complications like infection. In SLE, iliofemoral (IF) deep vein thrombosis (DVT) with fever and erythematous swollen limbs mimic cellulitis over lower extremities. Nevertheless, to distinguish DVT from cellulitis is imperative in clinical practice due to the use of different therapeutic regimens. Methods: A retrospective study was performed to analyze iliofemoral DVT in hospitalized SLE-associated APS patients with fever and erythematous swollen limbs mimicking cellulitis from January 1, 2011 to December 31, 2020. Results: Among 896 hospitalized SLE patients, 117 were associated with APS. Three patients had pelvic IF DVT with total vascular occlusion, presenting as fever and erythematous swollen limbs mimicking cellulitis. Despite negative duplex sonographic findings, IF thrombi were demonstrated by using computed tomography and/or catheter venography. Owing to refractory to unfractionated or low-molecular-weight heparin injection, all received the thrombolytic treatment. Complete resolution of thrombi without recurrent DVT and post-thrombotic syndrome was identified in two patients receiving pharmacomechanical thrombectomy or catheter-directed thrombolysis. Conclusions: For differential diagnosis of IF DVT and lower limb cellulitis in SLE-associated APS, our case series underlines the importance of venography to detect an unusual pelvic location of thrombi.
AB - Objectives: Systemic lupus erythematosus (SLE) associated with antiphospholipid syndrome (APS) is a complex clinical scenario with thromboembolic events, lupus activity, and related therapeutic complications like infection. In SLE, iliofemoral (IF) deep vein thrombosis (DVT) with fever and erythematous swollen limbs mimic cellulitis over lower extremities. Nevertheless, to distinguish DVT from cellulitis is imperative in clinical practice due to the use of different therapeutic regimens. Methods: A retrospective study was performed to analyze iliofemoral DVT in hospitalized SLE-associated APS patients with fever and erythematous swollen limbs mimicking cellulitis from January 1, 2011 to December 31, 2020. Results: Among 896 hospitalized SLE patients, 117 were associated with APS. Three patients had pelvic IF DVT with total vascular occlusion, presenting as fever and erythematous swollen limbs mimicking cellulitis. Despite negative duplex sonographic findings, IF thrombi were demonstrated by using computed tomography and/or catheter venography. Owing to refractory to unfractionated or low-molecular-weight heparin injection, all received the thrombolytic treatment. Complete resolution of thrombi without recurrent DVT and post-thrombotic syndrome was identified in two patients receiving pharmacomechanical thrombectomy or catheter-directed thrombolysis. Conclusions: For differential diagnosis of IF DVT and lower limb cellulitis in SLE-associated APS, our case series underlines the importance of venography to detect an unusual pelvic location of thrombi.
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U2 - 10.1177/09612033221084230
DO - 10.1177/09612033221084230
M3 - Article
C2 - 35293251
AN - SCOPUS:85126358506
SN - 0961-2033
VL - 31
SP - 613
EP - 618
JO - Lupus
JF - Lupus
IS - 5
ER -