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Lymphatic Embolization for the Treatment of Pelvic Lymphoceles: Preliminary Experience in Five Patients

Authors
Baek, YoolimWon, Je HwanChang, Suk-JoonRyu, Hee-SugSong, Soon-YoungYim, BonggukKim, Jinoo
Issue Date
Aug-2016
Publisher
ELSEVIER SCIENCE INC
Citation
JOURNAL OF VASCULAR AND INTERVENTIONAL RADIOLOGY, v.27, no.8, pp.1170 - 1176
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF VASCULAR AND INTERVENTIONAL RADIOLOGY
Volume
27
Number
8
Start Page
1170
End Page
1176
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/154179
DOI
10.1016/j.jvir.2016.04.011
ISSN
1051-0443
Abstract
Purpose To retrospectively assess the outcome of lymphatic embolization in the treatment of pelvic lymphoceles. Materials and Methods From July 2014 to December 2015, a retrospective analysis was performed in 5 consecutive female patients (mean age, 54.6 y; range, 45–65 y) who underwent lymphangiography for the management of symptomatic pelvic lymphoceles that developed after gynecologic surgery. Sclerotherapy had failed in 4 patients. Lymphangiography was performed through an inguinal lymph node to reveal disrupted lymphatic vessels draining into the lymphocele. This inflow vessel was targeted with a fine needle, and N -butyl cyanoacrylate (NBCA) was injected. Outcomes and complications were assessed by reviewing electronic medical records and computed tomography (CT). Results Lymphangiography revealed disrupted lymphatic vessels draining into the lymphocele in all patients. A single inflow vessel was seen in 3 patients and was subsequently embolized. Catheters were successfully removed upon decrease of drainage. Multiple inflow vessels were seen in the remaining 2 patients. Therapeutic effect was anticipated in 1 patient after lymphangiography alone, whereas only the dominant feeding vessel was embolized in the other. The initial procedures failed in both patients, prompting repeat embolization with adjunctive sclerotherapy. Both patients showed improvement and had their catheters removed. Follow-up CT was available in 3 patients. Two patients showed complete regression of lymphoceles, and 1 showed an asymptomatic lymphocele. No procedure-related complications occurred during a mean follow-up period of 35 weeks (range, 2–73 wk). Conclusions Lymphatic intervention was technically feasible in treating lymphoceles. However, those with multiple inflow vessels were relatively difficult to treat.
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