Zhao Jing, Yuan Jian-Jun, Dong Chang-Xian, Zhang Xiangqin, Li Chuang, Sun Qi, Wu Gang
Department of Ultrasounography, Zhengzhou University People's Hospital, Henan provincial People's Hospital, Zhengzhou City, China.
Department of Hemangioma and Vascular Malformation, Zhengzhou University People's Hospital, Henan provincial People's Hospital, Zhengzhou City, China.
Ultraschall Med. 2025 Jun;46(3):278-284. doi: 10.1055/a-2421-6047. Epub 2024 Oct 15.
Kaposiform hemangioendothelioma (KHE) is a rare, locally aggressive vascular tumor with high morbidity and mortality. The aim of this study was to evaluate ultrasonographic findings associated with KHE.The clinical and ultrasonographic findings of a cohort of 64 cases with pathologically proven KHE were retrospectively reviewed and analyzed between November 2014 and February 2021. Two subtypes were divided according to the presence or absence of the Kasabach-Merritt phenomenon (KMP). The KMP risk factors in patients with KHE were analyzed statistically.Among the 64 cases of KHE, 43 (67.2%) were accompanied by KMP. There was a positive correlation between the appearance of KMP and tumor size. KHEs had an increased risk of developing KMP if the lesions measured were >6 cm and if they belonged to the deep or mixed subtype. On ultrasonography, all KHE lesions were heterogeneous, and 81.3% were hypoechoic; 93.8% of KHEs exhibited ill-defined margins, 68.7% had strands branching into the adjacent tissue, and 84.4% presented marked hypervascularity. Elastography showed that central hypoechogenic lesion areas were hard, and surrounding hyperechogenic lesion areas were soft.KHEs can occur in different parts of childrens' bodies. On ultrasonography, the main findings are heterogeneous low erosions, indistinct margins, branching strangulation into adjacent tissues, and obvious hypervascularity. Patients with lesions larger than 6 cm or belonging to deep or mixed subtypes (musculoskeletal infiltrates) are at risk for developing KMP, and clinicians should be vigilant.
卡波西型血管内皮瘤(KHE)是一种罕见的、具有局部侵袭性的血管肿瘤,发病率和死亡率较高。本研究的目的是评估与KHE相关的超声检查结果。回顾性分析了2014年11月至2021年2月期间64例经病理证实为KHE患者的临床和超声检查结果。根据卡萨巴赫-梅里特现象(KMP)的有无将其分为两个亚型。对KHE患者的KMP危险因素进行了统计学分析。64例KHE患者中,43例(67.2%)伴有KMP。KMP的出现与肿瘤大小呈正相关。如果测量的病变>6 cm且属于深部或混合型,则KHE发生KMP的风险增加。超声检查显示,所有KHE病变均不均匀,81.3%为低回声;93.8%的KHE边界不清,68.7%有分支伸入相邻组织,84.4%表现为明显的高血管性。弹性成像显示,中央低回声病变区域硬,周围高回声病变区域软。KHE可发生于儿童身体的不同部位。超声检查的主要表现为不均匀的低回声、边界不清、分支伸入相邻组织以及明显的高血管性。病变大于6 cm或属于深部或混合型(肌肉骨骼浸润型)的患者有发生KMP的风险,临床医生应保持警惕。