Takayasu Kenichi, Muramatsu Yukio, Mizuguchi Yasunori, Okusaka Takuji, Shimada Kazuaki, Takayama Tadatoshi, Sakamoto Michiie
Department of Diagnostic Radiology, National Cancer Center Hospital, 5-1-1, Tsukiji, Chuo-ku, Tokyo 104-0045, Japan.
AJR Am J Roentgenol. 2006 Aug;187(2):454-63. doi: 10.2214/AJR.05.0705.
The purpose of this study was to clarify the natural outcomes of hypoattenuating nodular lesions in patients with virus-related chronic liver disease depicted on dynamic CT.
Sixty lesions (mean size, 1.3 cm) exhibiting hypoattenuation or isoattenuation in the arterial and delayed phases of dynamic CT were retrospectively evaluated with additional CT (mean, six examinations) for a mean period of 838 days. The primary end point was emergence of hyperattenuating areas within hypoattenuating lesions, a phenomenon called attenuation conversion. Cumulative attenuation conversion rates suggesting rates of malignant transformation were calculated with the Kaplan-Meier method, and factors affecting attenuation conversion rate were analyzed with the Cox proportional hazard model.
Thirty-six (60%) of 60 hypoattenuating lesions developed to hyperattenuating lesions, 21 were unchanged, and three disappeared spontaneously. The 36 lesions that became hyperattenuating were divided into two subgroups according to lesion enhancement pattern: hyper-in-hypoattenuating (n = 25) and entirely hyperattenuating (n = 11). The cumulative attenuation conversion rates for the 60 hypoattenuating lesions were 15.8%, 44.3%, and 58.7% at 1, 2, and 3 years. The hyper-in-hypoattenuating lesions showed more rapid progression to entirely enhanced lesions. Positive results for hepatitis C viral antibody (p = 0.028) and initial lesion size (p = 0.007) showed a positive correlation with attenuation conversion rate.
Hypoattenuating hepatic nodular lesions in chronic liver disease depicted on dynamic CT have high malignant potential and should be followed with special attention to conversion from hypoattenuation to hyperattenuation to determine the optimal timing of treatment.
本研究旨在阐明动态CT显示的病毒相关性慢性肝病患者中低密度结节性病变的自然转归。
回顾性评估60个病变(平均大小1.3 cm),这些病变在动态CT动脉期和延迟期表现为低密度或等密度,平均随访838天,期间进行了额外的CT检查(平均6次)。主要终点是低密度病变内出现高密度区域,即所谓的密度转换现象。采用Kaplan-Meier法计算提示恶性转化的累积密度转化率,并使用Cox比例风险模型分析影响密度转化率的因素。
60个低密度病变中有36个(60%)发展为高密度病变,21个病变无变化,3个病变自发消失。根据病变强化模式,36个变为高密度的病变分为两个亚组:低密度内高密度(n = 25)和完全高密度(n = 11)。60个低密度病变在1年、2年和3年的累积密度转化率分别为15.8%、44.3%和58.7%。低密度内高密度病变向完全强化病变的进展更快。丙型肝炎病毒抗体阳性结果(p = 0.028)和初始病变大小(p = 0.007)与密度转化率呈正相关。
动态CT显示的慢性肝病中的肝脏低密度结节性病变具有较高的恶性潜能,应密切随访,特别关注从低密度向高密度的转换,以确定最佳治疗时机。