Computed Tomography Perfusion, Magnetic Resonance Imaging, and Histopathological Findings After Laparoscopic Renal Cryoablation: An In Vivo Pig Model

• Published in: Technology in cancer research & treatment Vol. 16; no. 4; pp. 406 - 413
• Main Authors: Nielsen, Tommy Kjærgaard, Østraat, Øyvind, Graumann, Ole, Pedersen, Bodil Ginnerup, Andersen, Gratien, Høyer, Søren, Borre, Michael
• Format: Journal Article
• Language: English
• Published: Los Angeles, CA SAGE Publications 01-08-2017; Sage Publications Ltd
• Subjects: Animals; Computed tomography; Cryoablation; Cryosurgery; Female; Hemorrhage; Kidney - diagnostic imaging; Kidney - pathology; Kidney - surgery; Kidney cancer; Kidney Neoplasms - diagnostic imaging; Kidney Neoplasms - surgery; Kidneys; Laparoscopy; Magnetic Resonance Imaging; Nephrectomy; Nephrectomy - methods; Parenchyma; Perfusion; Sus scrofa; Tomography; Tomography, X-Ray Computed; Treatment Outcome; Urothelium; computed tomography; kidney cancer; CT-perfusion; pathology; cryoablation; cryo surgery; animal; MRI scan
• ISSN: 1533-0346; 1533-0338
• DOI: 10.1177/1533034616657251

The present study investigates how computed tomography perfusion scans and magnetic resonance imaging correlates with the histopathological alterations in renal tissue after cryoablation. A total of 15 pigs were subjected to laparoscopic-assisted cryoablation on both kidneys. After intervention, each animal was randomized to a postoperative follow-up period of 1, 2, or 4 weeks, after which computed tomography perfusion and magnetic resonance imaging scans were performed. Immediately after imaging, open bilateral nephrectomy was performed allowing for histopathological examination of the cryolesions. On computed tomography perfusion and magnetic resonance imaging examinations, rim enhancement was observed in the transition zone of the cryolesion 1week after laparoscopic-assisted cryoablation. This rim enhancement was found to subside after 2 and 4 weeks of follow-up, which was consistent with the microscopic examinations revealing of fibrotic scar tissue formation in the peripheral zone of the cryolesion. On T2 magnetic resonance imaging sequences, a thin hypointense rim surrounded the cryolesion, separating it from the adjacent renal parenchyma. Microscopic examinations revealed hemorrhage and later hemosiderin located in the peripheral zone. No nodular or diffuse contrast enhancement was found in the central zone of the cryolesions at any follow-up stage on neither computed tomography perfusion nor magnetic resonance imaging. On microscopic examinations, the central zone was found to consist of coagulative necrosis 1 week after laparoscopic-assisted cryoablation, which was partially replaced by fibrotic scar tissue 4 weeks following laparoscopic-assisted cryoablation. Both computed tomography perfusion and magnetic resonance imaging found the renal collecting system to be involved at all 3 stages of follow-up, but on microscopic examination, the urothelium was found to be intact in all cases. In conclusion, cryoablation effectively destroyed renal parenchyma, leaving the urothelium intact. Both computed tomography perfusion and magnetic resonance imaging reflect the microscopic findings but with some differences, especially regarding the peripheral zone. Magnetic resonance imaging seems an attractive modality for early postoperative follow-up.