Histologic changes of porcine portal vein anastomosis after electrochemotherapy with bleomycin
•Electroporation and electrochemotherapy with bleomycin caused endotheliitis.•They also caused vascular smooth muscle cell destruction in portal vein anastomosis.•Regeneration of endothelium and organization of fibrosis was seen after 28 days.•Histology of the treated veins were consistent with norm...
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| Published in: | Bioelectrochemistry (Amsterdam, Netherlands) Vol. 154; p. 108509 |
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| Language: | English |
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| Abstract | •Electroporation and electrochemotherapy with bleomycin caused endotheliitis.•They also caused vascular smooth muscle cell destruction in portal vein anastomosis.•Regeneration of endothelium and organization of fibrosis was seen after 28 days.•Histology of the treated veins were consistent with normal healing process.•Electrochemotherapy of portal vein anastomosis is safe and feasible.
Electrochemotherapy (ECT11Electrochemotherapy.) is used for treatment of unresectable abdominal malignancies. This study aims to show that ECT of porcine portal vein anastomosis is safe and feasible in order to extend the indications for margin attenuation after resection of locally advanced pancreatic carcinoma. No marked differences were found between the control group and ECT treated groups. Electroporation thus caused irreversible damage to the vascular smooth muscle cells in tunica media that could bedue to the narrow irreversible electroporation zone that may occur near the electrodes, or due to vasa vasorum thrombosis in the tunica externa. Based on the absence of vascular complications, and similar histological changes in lienal veinanastomosis, we can conclude that ECT of portal vein anastomosis is safe and feasible. |
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| AbstractList | Electrochemotherapy (ECT1) is used for treatment of unresectable abdominal malignancies. This study aims to show that ECT of porcine portal vein anastomosis is safe and feasible in order to extend the indications for margin attenuation after resection of locally advanced pancreatic carcinoma. No marked differences were found between the control group and ECT treated groups. Electroporation thus caused irreversible damage to the vascular smooth muscle cells in tunica media that could bedue to the narrow irreversible electroporation zone that may occur near the electrodes, or due to vasa vasorum thrombosis in the tunica externa. Based on the absence of vascular complications, and similar histological changes in lienal veinanastomosis, we can conclude that ECT of portal vein anastomosis is safe and feasible.Electrochemotherapy (ECT1) is used for treatment of unresectable abdominal malignancies. This study aims to show that ECT of porcine portal vein anastomosis is safe and feasible in order to extend the indications for margin attenuation after resection of locally advanced pancreatic carcinoma. No marked differences were found between the control group and ECT treated groups. Electroporation thus caused irreversible damage to the vascular smooth muscle cells in tunica media that could bedue to the narrow irreversible electroporation zone that may occur near the electrodes, or due to vasa vasorum thrombosis in the tunica externa. Based on the absence of vascular complications, and similar histological changes in lienal veinanastomosis, we can conclude that ECT of portal vein anastomosis is safe and feasible. Electrochemotherapy (ECT ) is used for treatment of unresectable abdominal malignancies. This study aims to show that ECT of porcine portal vein anastomosis is safe and feasible in order to extend the indications for margin attenuation after resection of locally advanced pancreatic carcinoma. No marked differences were found between the control group and ECT treated groups. Electroporation thus caused irreversible damage to the vascular smooth muscle cells in tunica media that could bedue to the narrow irreversible electroporation zone that may occur near the electrodes, or due to vasa vasorum thrombosis in the tunica externa. Based on the absence of vascular complications, and similar histological changes in lienal veinanastomosis, we can conclude that ECT of portal vein anastomosis is safe and feasible. •Electroporation and electrochemotherapy with bleomycin caused endotheliitis.•They also caused vascular smooth muscle cell destruction in portal vein anastomosis.•Regeneration of endothelium and organization of fibrosis was seen after 28 days.•Histology of the treated veins were consistent with normal healing process.•Electrochemotherapy of portal vein anastomosis is safe and feasible. Electrochemotherapy (ECT11Electrochemotherapy.) is used for treatment of unresectable abdominal malignancies. This study aims to show that ECT of porcine portal vein anastomosis is safe and feasible in order to extend the indications for margin attenuation after resection of locally advanced pancreatic carcinoma. No marked differences were found between the control group and ECT treated groups. Electroporation thus caused irreversible damage to the vascular smooth muscle cells in tunica media that could bedue to the narrow irreversible electroporation zone that may occur near the electrodes, or due to vasa vasorum thrombosis in the tunica externa. Based on the absence of vascular complications, and similar histological changes in lienal veinanastomosis, we can conclude that ECT of portal vein anastomosis is safe and feasible. |
| ArticleNumber | 108509 |
| Author | Plut, Jan Plavec, Tanja Trotovšek, Blaž Petrič, Miha Seliškar, Alenka Lampreht Tratar, Urša Jesenko, Tanja Čemažar, Maja Štukelj, Marina Ranković, Branislava Đokić, Mihajlo Gašljević, Gorana Serša, Gregor Nemec Svete, Alenka Stupan, Urban Sredenšek, Jerneja Tomažič, Aleš |
| Author_xml | – sequence: 1 givenname: Urban surname: Stupan fullname: Stupan, Urban email: urban.stupan@kclj.si organization: University of Ljubljana, Faculty of Medicine, Korytkova ulica 2, SI-1000 Ljubljana, Slovenia – sequence: 2 givenname: Maja surname: Čemažar fullname: Čemažar, Maja organization: Institute of Oncology Ljubljana, Zaloška cesta 2, SI-1000 Ljubljana, Slovenia – sequence: 3 givenname: Blaž surname: Trotovšek fullname: Trotovšek, Blaž organization: University of Ljubljana, Faculty of Medicine, Korytkova ulica 2, SI-1000 Ljubljana, Slovenia – sequence: 4 givenname: Miha surname: Petrič fullname: Petrič, Miha organization: University of Ljubljana, Faculty of Medicine, Korytkova ulica 2, SI-1000 Ljubljana, Slovenia – sequence: 5 givenname: Aleš surname: Tomažič fullname: Tomažič, Aleš organization: University of Ljubljana, Faculty of Medicine, Korytkova ulica 2, SI-1000 Ljubljana, Slovenia – sequence: 6 givenname: Gorana surname: Gašljević fullname: Gašljević, Gorana organization: Institute of Oncology Ljubljana, Zaloška cesta 2, SI-1000 Ljubljana, Slovenia – sequence: 7 givenname: Branislava surname: Ranković fullname: Ranković, Branislava organization: University of Ljubljana, Faculty of Medicine, Korytkova ulica 2, SI-1000 Ljubljana, Slovenia – sequence: 8 givenname: Alenka surname: Seliškar fullname: Seliškar, Alenka organization: University of Primorska, Faculty of Health Sciences, Polje 42, SI-6310 Izola, Slovenia – sequence: 9 givenname: Tanja surname: Plavec fullname: Plavec, Tanja organization: University of Primorska, Faculty of Health Sciences, Polje 42, SI-6310 Izola, Slovenia – sequence: 10 givenname: Jerneja surname: Sredenšek fullname: Sredenšek, Jerneja organization: University of Primorska, Faculty of Health Sciences, Polje 42, SI-6310 Izola, Slovenia – sequence: 11 givenname: Jan surname: Plut fullname: Plut, Jan organization: University of Primorska, Faculty of Health Sciences, Polje 42, SI-6310 Izola, Slovenia – sequence: 12 givenname: Marina surname: Štukelj fullname: Štukelj, Marina organization: University of Primorska, Faculty of Health Sciences, Polje 42, SI-6310 Izola, Slovenia – sequence: 13 givenname: Urša surname: Lampreht Tratar fullname: Lampreht Tratar, Urša organization: Institute of Oncology Ljubljana, Zaloška cesta 2, SI-1000 Ljubljana, Slovenia – sequence: 14 givenname: Tanja surname: Jesenko fullname: Jesenko, Tanja organization: Institute of Oncology Ljubljana, Zaloška cesta 2, SI-1000 Ljubljana, Slovenia – sequence: 15 givenname: Alenka surname: Nemec Svete fullname: Nemec Svete, Alenka organization: University of Primorska, Faculty of Health Sciences, Polje 42, SI-6310 Izola, Slovenia – sequence: 16 givenname: Gregor surname: Serša fullname: Serša, Gregor organization: Institute of Oncology Ljubljana, Zaloška cesta 2, SI-1000 Ljubljana, Slovenia – sequence: 17 givenname: Mihajlo surname: Đokić fullname: Đokić, Mihajlo organization: University of Ljubljana, Faculty of Medicine, Korytkova ulica 2, SI-1000 Ljubljana, Slovenia |
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| Keywords | Electrochemotherapy Pancreatic cancer Portal vein anastomosis |
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| Title | Histologic changes of porcine portal vein anastomosis after electrochemotherapy with bleomycin |
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