Difference in microvascular structure between benign and malignant pulmonary nodules and its relationship with CT enhancement
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Difference in microvascular structure between benign and malignant pulmonary nodules and its relationship with CT enhancement
Military Medical ResearchIssue 4, Pages: 243-248(2006)
Affiliations:
1. Department of Radiology Changzheng Hospital
2. Second Military Medical University
3. ,China
4. Department of Pathology
Author bio:
Funds:
DOI:
CLC:R816.4
Published:2006
Accepted:
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[1]刘士远,杨春山,李慎江,顾倩,肖湘生,冯云,李成洲,李惠民,李玉莉,刘会敏.Difference in microvascular structure between benign and malignant pulmonary nodules and its relationship with CT enhancement[J].Journal of Medical Colleges of PLA,2006(04):243-248.
DOI:
[1]刘士远,杨春山,李慎江,顾倩,肖湘生,冯云,李成洲,李惠民,李玉莉,刘会敏.Difference in microvascular structure between benign and malignant pulmonary nodules and its relationship with CT enhancement[J].Journal of Medical Colleges of PLA,2006(04):243-248.DOI:
Difference in microvascular structure between benign and malignant pulmonary nodules and its relationship with CT enhancement
摘要
Abstract
<正>Objective: To investigate the enhancement basis and the mechanisms of solitary pulmonary nodules (SPNs) by comparing the differences in microvascular structure between benign and malignant lesions. Methods: Dynamic contrast-enhanced CT scan was performed on 53 patients with SPNs (diameter<3 cm. 38 peripheral lung cancers
5 hamartomas
10 inflammatory lesions) using a Siemens Plus S or a Marconi MX8000 multi-slices spiral CT scanner. The time-attenuation curves were interpreted. The microvascular density (MVD) and the continuity of the microvessels’ basemental membrane in the dissected specimens were observed with the ABC (avidin-biotin-complex) immuno-histochemical method in all patients. ResultS:The CT enhancement values of lung cancer (49. 05±16. 08 HU) and inflammatory lesions (49. 59±21. 30 HU) were significantly higher than those of hamartoma (8. 98±4. 56 HU) (t = 7. 48. P<0. 05; t = 8. 35
P<0. 05). But the enhancement of lung cancer was similar to that of inflammatory lesions (t = 0. 76. P>0. 05). The time-attenuation curve of inflammatory lesions tended to increase faster and reached a higher peak compared to the lung cancer
and both of them maintained a high plateau after crossing. The hamartoma showed a slight increase in the time-attenuation curve and demonstrated a low-plateau curve. The MVD of SPNs was positively correlated with CT enhancement (r=0. 8051). The microvascular counts of peripheral lung cancer (48. 45±10. 09) and inflammatory lesions (19. 60±19. 94) were significantly higher than those of hamartoma (8.70±7.30) (t = 11.64
P<0.001;t = 6. 09. P< 0. 001). but no significant difference was found between lung cancer and inflammatory lesions (t= -0. 26
P = (). 799). There was no difference in the continuity of basement membrane between nodules with an enhancement less than 30 HU and those with an enhancement higher than 30HU (x2 = 3. 13
P>0. 05 ). Conclusion: The microvascular counts mainly contribute to the enhancement value of SPNs. The basement membrane is not related to nodule enhancement
but it might influence the pattern of the time-attenuation curve.
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