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- 저자 : Nicolas Levi (검색결과 3 건)
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Historical Relations between Poland and North Korea from 1948 to 1980
Nicolas Levi,문경연 통일연구원 2018 International journal of korean unification studie Vol.27 No.1
This article focuses on relations between Poland and North Korea from 1948 till 1980, focusing on places of remembrance of Poles in North Korea, and North Korean citizens in Poland. During this period, bilateral relations between these countries were very close due to their belonging to the same ideological movement. The article focuses on political, ideological, cultural, and economic relations based on three historical phases of the Korean War (1950-1953), Post-Korean War (1953-1960) and disturbance of Poland-North Korea relations (1960-1980). The paper argues that although Poland did make efforts to successfully foster mutual relations, sometimes regardless of Polish interest, the behavior of DPRK authorities reduced the benefits Poland could gain from maintaining relations with this country. The DPRK focused on its interest and not on the interest of fraternal nations. This led to a negative image of the DPRK authorities among the Polish leadership and automatically to negative views concerning the DPRK population among Poles.
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Celeste Del Basso,Roberto Luca Meniconi,Sofia Usai,Nicola Guglielmo,Marco Colasanti,Stefano Ferretti,Giovanni Battista Levi Sandri,Giuseppe Maria Ettorre 한국간담췌외과학회 2021 Annals of hepato-biliary-pancreatic surgery Vol.25 No.3
Portal vein arterialization (PVA) has been attracting attention for its role as a salvage inflow technique in various clinical applications. Initially performed in shunt surgery for portal hypertension, with the aim of preventing a decreased hepatic inflow, it is largely used in case of hepatic artery thrombosis in the transplantation domain or in the enlarged radical operations in case of hilar cancer invading the hepatic artery. A 62-year-old man underwent a left extended hepatectomy with hepatic bile duct resection and right Roux-en-Y hepaticojejunostomy for hilar cholangiocarcinoma. Computed tomography scan on postoperative day (POD) 5 revealed right hepatic artery pseudo-aneurysm, which was confirmed by an angiography. Stent placement was infeasible. Coiling of the pseudoaneurysm was associated with a risk of complete occlusion inducing critical liver failure. Since his general conditions were deteriorated, the patient underwent an emergency laparotomy. Hepatic artery reconstruction was impossible. Thus, a PVA was performed by anastomosing the ileocecal artery and vein. The intraoperative ultrasound showed satisfactory patency of the PVA with good portal flow in the absence of arterial flow. Doppler ultrasound on POD 15 showed that the cross-sectional area and blood flow of the portal vein were increased. The patient was discharged on POD 54 in good general condition. Hepatic artery disruption represents potentially lethal complications of hepatic, biliary, and pancreatic surgery. PVA may be a feasible therapeutic strategy to guarantee arterial inflow to the remnant liver. Although PVA is a salvage surgical procedure, increased portal flow should be controlled to avoid portal hypertension and liver fibrosis.
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( Deren Ozcan ),( Murat Derbent ),( Deniz Seckin ),( Yunus Emre Bikmaz ),( Muhtesem Agildere ),( Annachiara De Sandre Giovannoli ),( Nicolas Levy ),( Berkan Gurakan ) 대한피부과학회 2013 Annals of Dermatology Vol.25 No.4
Neu-Laxova syndrome is a rare, lethal, autosomal recessive disorder characterized by intrauterine growth retardation, central nervous system anomalies, skin findings, such as ichthyosis, edema, collodion baby and harlequin fetus, facial dysmorphic features, limb anomalies and genital hypoplasia. Although it is generally a lethal condition, cases of such patients who lived beyond 6 months and 10 months of age have been reported. Here, we describe an 8-year-old boy who was born with collodion membrane, facial dysmorphic features, limb anomalies, genital hypoplasia and pachygyria. He had no major health problems over the course of 8 years of follow-up, except for mild mental/motor retardation, ichthyosis, facial dysmorphic features and limb anomalies. Based on these features, we suggest that because Neu-Laxova syndrome represents a heterogeneous phenotype, our case may be a milder variant of this syndrome or a new genetic entity. (Ann Dermatol 25(4) 483∼488, 2013)
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