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Erschienen in: Abdominal Radiology 5/2010

01.10.2010

Angiogenesis of renal cell carcinoma: perfusion CT findings

verfasst von: Yan Chen, Jin Zhang, Jingrui Dai, Xiaoli Feng, Haizhen Lu, Chunwu Zhou

Erschienen in: Abdominal Radiology | Ausgabe 5/2010

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Abstract

Objective

To observe the perfusion CT findings of renal cell carcinoma (RCC) and prospectively correlate perfusion CT parameters with tumor MVD and VEGF expression.

Methods

Dynamic contrast-enhanced multislice spiral CT was performed prospectively in 73 cases with histologically proven RCC (65 clear cell, 3 papillary, and 5 chromophobe). Blood flow (BF), blood volume (BV), mean transit time (MTT), and permeability surface-area product (PS) of RCC and normal renal cortex were measured, respectively. The tumor MVD count and VEGF expression level were determined by immunohistochemistry with specific monoclonal antibodies.

Results

There was significant difference between BF, BV, MTT, and PS of normal renal cortex (454.32 ± 110.90 mL/min/100 g, 23.53 ± 5.71 mL/100 g, 3.62 ± 1.38 s, 63.95 ± 18.85 mL/min/100 g) and RCC (261.96 ± 175.86 mL/min/100 g, 17.17 ± 8.34 mL/100 g, 7.08 ± 3.42 s, 25.07 ± 13.20 mL/min/100 g) (P < 0.01). BF and BV among RCC histologic subtypes were significantly different (P < 0.05), MTT and PS were not (P > 0.05). MVD (42.29 ± 21.00) of RCC is positively correlated with BF, BV, and PS (P < 0.01), not with MTT (P > 0.05). No relationship was found between the expression levels of VEGF and any perfusion CT parameter.

Conclusions

Perfusion CT is a feasible technique to assess tissue perfusion in patients with RCC. BV, BF, and PS correlate positively with MVD and may reflect angiogenesis of RCC.
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Metadaten
Titel
Angiogenesis of renal cell carcinoma: perfusion CT findings
verfasst von
Yan Chen
Jin Zhang
Jingrui Dai
Xiaoli Feng
Haizhen Lu
Chunwu Zhou
Publikationsdatum
01.10.2010
Verlag
Springer-Verlag
Erschienen in
Abdominal Radiology / Ausgabe 5/2010
Print ISSN: 2366-004X
Elektronische ISSN: 2366-0058
DOI
https://doi.org/10.1007/s00261-009-9565-0

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