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本文引用的文献

1
A Case of Superficial Kaposiform Hemangioendothelioma Treated with Oral Propranolol Combined with Topical Sirolimus.口服普萘洛尔联合外用西罗莫司治疗浅表性血管球瘤样血管内皮细胞瘤 1 例
Vasc Health Risk Manag. 2024 Jun 12;20:251-254. doi: 10.2147/VHRM.S461505. eCollection 2024.
2
Kaposiform Hemangioendothelioma with Bone Destruction: A 16-Year Follow-Up Cohort Study of the Clinical Characteristics and Prognosis.伴有骨质破坏的颅颊型血管内皮细胞瘤:16 年临床特征和预后的随访队列研究。
J Pediatr Surg. 2024 Apr;59(4):599-604. doi: 10.1016/j.jpedsurg.2023.12.003. Epub 2023 Dec 7.
3
Treatment practices and response in kaposiform hemangioendothelioma: A multicenter cohort study.卡波西样血管内皮细胞瘤的治疗方法和疗效:一项多中心队列研究。
Pediatr Blood Cancer. 2024 Mar;71(3):e30779. doi: 10.1002/pbc.30779. Epub 2023 Dec 10.
4
Kaposiform hemangioendothelioma complicated by Kasabach-Merritt phenomenon in an infant girl.一名女婴患卡波西型血管内皮瘤并伴有卡萨巴赫-梅里特现象。
Clin Case Rep. 2023 Sep 13;11(9):e7859. doi: 10.1002/ccr3.7859. eCollection 2023 Sep.
5
Kaposiform hemangioendothelioma of skull base with dura invasion in a pediatric patient: a case report.颅骨底部伴有硬脑膜侵犯的婴儿Kaposiform 血管内皮细胞瘤:1 例报告。
Childs Nerv Syst. 2023 Nov;39(11):3289-3294. doi: 10.1007/s00381-023-06025-9. Epub 2023 Jun 24.
6
Kaposiform hemangioendothelioma of the heart: a case report and literature review.心脏卡波西样血管内皮细胞瘤:病例报告及文献复习。
Cardiol Young. 2023 Nov;33(11):2411-2414. doi: 10.1017/S1047951123001269. Epub 2023 Jun 19.
7
Platelet functional abnormalities in pediatric patients with kaposiform hemangioendothelioma/Kasabach-Merritt phenomenon.儿科患者伴血小板功能异常的kaposiform 血管内皮细胞瘤/卡波西样血管内皮瘤现象。
Blood Adv. 2023 Sep 12;7(17):4936-4949. doi: 10.1182/bloodadvances.2022009590.
8
Impact of age and tumor size on the development of the Kasabach-Merritt phenomenon in patients with kaposiform hemangioendothelioma: a retrospective cohort study.年龄和肿瘤大小对卡波西样血管内皮瘤患者卡萨巴赫-梅里特现象发生发展的影响:一项回顾性队列研究
Precis Clin Med. 2023 May 19;6(2):pbad008. doi: 10.1093/pcmedi/pbad008. eCollection 2023 Jun.
9
Clinical and imaging features of Kaposiform hemangioendothelioma in infants.婴儿卡波西样血管内皮瘤的临床及影像学特征
Heliyon. 2023 Apr 10;9(5):e15425. doi: 10.1016/j.heliyon.2023.e15425. eCollection 2023 May.
10
Multivertebral Kaposiform hemangioendothelioma presenting as scoliosis - A case report and review of literature.表现为脊柱侧弯的多椎体卡波西样血管内皮瘤——病例报告及文献复习
J Clin Orthop Trauma. 2023 Mar 17;39:102147. doi: 10.1016/j.jcot.2023.102147. eCollection 2023 Apr.

基于超声影像组学的卡波西样血管内皮瘤的诊断与鉴别诊断

Diagnosis and differentiation of Kaposiform hemangioendothelioma based on ultrasound radiomics.

作者信息

Li Chuang, Dong Weihong, Li Yawei

机构信息

Department of Ultrasound, Henan Provincial People's Hospital, Zhengzhou University People's Hospital Zhengzhou 450003, Henan, China.

出版信息

Am J Cancer Res. 2024 Oct 15;14(10):4935-4945. doi: 10.62347/AQSJ3784. eCollection 2024.

DOI:10.62347/AQSJ3784
PMID:39553205
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11560810/
Abstract

Kaposiform hemangioendothelioma (KHE) is a rare neoplasm of the newborn, but has a very high mortality rate. In this study, we explore the application value of ultrasound radiomics in the differential diagnosis of KHE so as to provide reference for early diagnosis of KHE. We selected 194 cases of children with suspected KHE admitted to Henan Provincial People's Hospital from March 2016 to April 2024 for this retrospective analysis. All children completed ultrasound examinations in our hospital. After pathological biopsy, 132 cases were diagnosed with KHE. Taking pathological biopsy as the gold standard, the diagnostic rate of ultrasound examination was determined. Our results showed that ultrasound examination diagnosed 124 cases with KHE. Compared with pathological biopsy, the diagnostic sensitivity, specificity, and accuracy of ultrasound were 81.82, 77.42, and 80.41%, respectively (Kappa = 0.725). Most of the children had a single lesion, often involving the skin. The tumor was hard in texture and red or purple in color and did not fade when pressed. The two-dimensional sonogram showed a solid heterogeneous echo mass in the soft tissue. The lesion was generally large, irregular in shape, and unclear in boundaries, extending to the adipose layer and forming a "tree root-like" change. Microscopically, crossed spindle-shaped cell bundles could be seen, showing diffuse multinodular infiltrative growth. Children with the Kasabach-Merritt phenomenon (KMP) generally had larger lesions. Subsequently, the children with KHE were assigned to a training set and a validation set in a ratio of 7:3. High-throughput data acquisition of the regions of interest (ROIs) on the ultrasound images was carried out to construct a KEH prediction model based on ultrasound radiomics, and validation analysis was conducted. We found the diagnostic accuracy rate of ultrasound radiomics was 91.41%, the sensitivity was 77.44%, and the specificity was 97.21%, which were better than those of the conventional ultrasound. In conclusion, ultrasound radiomics analysis is highly effective in the diagnosis of KHE, which can contribute to the early diagnosis rate of KHE.

摘要

卡波西样血管内皮瘤(KHE)是一种罕见的新生儿肿瘤,但死亡率很高。在本研究中,我们探讨超声影像组学在KHE鉴别诊断中的应用价值,为KHE的早期诊断提供参考。我们选取了2016年3月至2024年4月在河南省人民医院收治的194例疑似KHE患儿进行回顾性分析。所有患儿均在我院完成超声检查。经病理活检后,132例被诊断为KHE。以病理活检为金标准,确定超声检查的诊断率。我们的结果显示,超声检查诊断出124例KHE。与病理活检相比,超声的诊断敏感性、特异性和准确性分别为81.82%、77.42%和80.41%(Kappa = 0.725)。大多数患儿为单发病变,常累及皮肤。肿瘤质地硬,颜色为红色或紫色,按压不褪色。二维超声图像显示软组织内实性不均匀回声团块。病变一般较大,形态不规则,边界不清,延伸至脂肪层并形成“树根样”改变。显微镜下可见交叉的梭形细胞束,呈弥漫性多结节浸润性生长。患有卡萨巴赫-梅里特现象(KMP)的患儿病变通常较大。随后,将KHE患儿按7:3的比例分为训练集和验证集。对超声图像上的感兴趣区域(ROI)进行高通量数据采集,构建基于超声影像组学的KEH预测模型,并进行验证分析。我们发现超声影像组学的诊断准确率为91.41%,敏感性为77.44%,特异性为97.21%,均优于传统超声。综上所述,超声影像组学分析在KHE诊断中具有很高的效能,有助于提高KHE的早期诊断率。