Chemoembolization Via Branches from the Splenic Artery in Patients with Hepatocellular Carcinoma

Chemoembolization Via Branches from the Splenic Artery in Patients with Hepatocellular Carcinoma

  • نوع فایل : کتاب
  • زبان : انگلیسی
  • مؤلف : Jin Woo Choi Hyo-Cheol Kim Jin Wook Chung Ji Dae Kim Gyoung Min Kim In Joon Lee Hwan Jun Jae Jae Hyung Park
  • چاپ و سال / کشور: 2011

Description

Purpose This study was designed to evaluate the radiologic findings and imaging response of chemoembolization via branches of the splenic artery in patients with hepatocellular carcinoma (HCC). Methods From January 2001 to July 2010, we observed tumor staining supplied by branches of the splenic artery in 34 (0.6%) of 5,413 patients with HCC. Computed tomography (CT) scans and digital subtraction angiograms of these patients were retrospectively reviewed in consensus by two investigators. Results A total of 39 tumor feeding-vessels in 34 patients were identified: omental branches from the left gastroepiploic artery (n = 5), branches from the short gastric artery (n = 9), and omental branches directly from the splenic artery (n = 25). Branches of the splenic artery that supplied tumors were revealed on the celiac angiogram in 29 (85%) of 34 patients and were detected on pre-procedure CT images in 27 (79%) of 34 patients. Selective chemoembolization was achieved in 38 of 39 tumor-feeding vessels. Complete or partial response of the tumor fed by branches of the splenic artery, as depicted on follow-up CT scans, was achieved in 21 (62%) patients. No patient developed severe complications directly related to chemoembolization via branches of the splenic artery. Conclusions Omental branches directly from the splenic artery are common tumor-feeding vessels of the splenic artery in cases of advanced HCC with multiple previous chemoembolizations. Tumor-feeding vessels of the splenic artery are usually visualized on the celiac angiogram or CT scan, and chemoembolization through them can be safely performed in most patients
Cardiovasc Intervent Radiol Received: 1 November 2010 / Accepted: 12 January 2011
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