Hu Pei-An, Zhou Zheng-Rong
1 Department of Radiology, Shanghai Institute of Medical Imaging , Shanghai , China.
2 Department of Radiology, Children's Hospital of Fudan University , Shanghai , China.
Br J Radiol. 2018 Jun;91(1086):20170798. doi: 10.1259/bjr.20170798. Epub 2018 Mar 20.
Kaposiform hemangioendothelioma (KHE) is a unique locally aggressive vascular tumor with poor prognosis. The aim of this study is to assess the clinical and imaging features of KHE, and to compare the differences between solitary and diffusive infiltrative subtype further.
The clinical and radiological findings of a cohort of 25 cases with histologically proven KHE, between June 2011 and June 2016, were reviewed retrospectively. 7 solitary and 18 diffusive infiltrative subtypes KHE were included. The differences of clinical and imaging features between these two subtypes were compared statistically by Wilcoxon rank sum test and Fisher exact test.
The median age was 4 months old. 20 cases (80%) were accompanied by Kasabach-Merritt phenomenon (KMP). Most KHE located in trunk and/or extremity. The masses showed inhomogeneous echogenicity and were rich in vascularity on ultrasound; showed isoattenuation relative to muscle on unenhanced CT, isointense (n = 15) or slightly hyperintense (n = 7) T weighted imaging (TWI) signal relative to muscle, mainly heterogeneous hyperintense or slightly hyperintense with speckled hypointense (n = 17) TWI signal (77%) relative to muscle, and notable (n = 15) and moderate (n = 3) enhancement. Feeding and draining vessels were revealed in 15 cases. Five masses with DWI showed slightly restricted diffusivity, with average apparent diffusion coefficient value of (1.28 ± 0.09) × 10 mm s. Necrosis and hemorrhage were also found. Compared with solitary ones, diffusive infiltrative KHE were larger, more commonly accompanied by KMP and reticular lymphedema, and more frequently located in trunk and/or extremity.
Five masses with DWI showed slightly restricted diffusivity. A hypervascular mass accompanied by KMP and reticular lymphedema, with speckled hypointense signal TWI signal, especially in pediatric patients, is highly suggestive of the diagnosis of KHE. Advances in knowledge: Speckled hypointense signal TWI signal, and notable enhancement were unique features of KHE. KHE showed slightly restricted diffusivity on DWI, commonly accompanied by KMP and reticular lymphedema.
卡波西样血管内皮瘤(KHE)是一种独特的局部侵袭性血管肿瘤,预后较差。本研究旨在评估KHE的临床和影像学特征,并进一步比较孤立型和弥漫浸润型亚型之间的差异。
回顾性分析2011年6月至2016年6月期间25例经组织学证实的KHE患者的临床和影像学资料。其中包括7例孤立型和18例弥漫浸润型KHE。采用Wilcoxon秩和检验和Fisher确切检验对这两种亚型的临床和影像学特征差异进行统计学比较。
中位年龄为4个月。20例(80%)伴有卡萨巴赫-梅里特现象(KMP)。大多数KHE位于躯干和/或四肢。肿块在超声上表现为回声不均匀且血管丰富;在平扫CT上相对于肌肉呈等密度,在T加权成像(TWI)上相对于肌肉呈等信号(n = 15)或稍高信号(n = 7),主要为不均匀高信号或稍高信号伴散在低信号(n = 17)(77%),且有明显(n = 15)和中等(n = 3)强化。15例显示有供血和引流血管。5个DWI上的肿块表现为轻度扩散受限,平均表观扩散系数值为(1.28 ± 0.09)×10⁻³mm²/s。还发现有坏死和出血。与孤立型相比,弥漫浸润型KHE体积更大,更常伴有KMP和网状淋巴水肿,且更常位于躯干和/或四肢。
5个DWI上的肿块表现为轻度扩散受限。伴有KMP和网状淋巴水肿、TWI上有散在低信号的高血管肿块,尤其是在儿科患者中,高度提示KHE的诊断。知识进展:TWI上的散在低信号和明显强化是KHE的独特特征。KHE在DWI上表现为轻度扩散受限,常伴有KMP和网状淋巴水肿。