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DOI 10.1016/j.currproblcancer.2019.04.002

Медицинская библиотека · Current problems in cancer · 2019

Portal vein stent for symptomatic malignant portal vein stenosis: A single-center experience.

Park Joo Hwan, Yeo Ja Hyun, Kim Young Saing, Ahn Hee Kyung, Sym Sunjin, Shin Dongbok, Hwang Junghan, Park Inkeun, Kim Jeong Ho

Клиническое исследованиеСтатьяПеревод пока не подготовлен

Аннотация

OBJECTIVE

Malignant tumors around the portal vein (PV) can cause PV stenosis, and PV stent (PVS) placement may reduce symptoms. This study aimed to investigate the efficacy and safety of PVS for symptomatic malignant PV stenosis.

METHODS

Fourteen consecutive patients who underwent percutaneous transhepatic PVS placement from January 2016 to August 2018 for symptomatic malignant PV stenosis were included. Medical records were retrospectively reviewed for procedure-related complications, symptom relief, and stent patency duration after PVS.

RESULTS

Of 14 patients, 7 (50%) were men (median age, 67.5 [range 32-76] years). The most common primary cancer site was the pancreas (57%). PVS placement and complete stent expansion were successful in 13 (93%) patients. PV stenosis-related symptoms were resolved in most patients, 13 of 14 (93%). There was a significant decline in median PV pressure gradient across the stenotic lesions. Postprocedural complications included 1 case (7%) each of hemothorax, intrahepatic PV thrombosis, and liver abscess. With a median follow-up of 114 (range 25-260) days, stent occlusion occurred in 5 patients (36%). The median stent patency duration was 201 days, and the overall survival was 117 days.

CONCLUSIONS

PVS placement is a safe and effective method for relieving the symptom of of malignant PV stenosis.

Для цитирования: Park Joo Hwan, Yeo Ja Hyun, Kim Young Saing, Ahn Hee Kyung, Sym Sunjin, Shin Dongbok, Hwang Junghan, Park Inkeun, Kim Jeong Ho. Portal vein stent for symptomatic malignant portal vein stenosis: A single-center experience.. Current problems in cancer. 2019. DOI: 10.1016/j.currproblcancer.2019.04.002.

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