Suppr超能文献

三角肌中无卡波西-梅格斯现象的卡波西样血管内皮细胞瘤。

Kaposiform hemangioendothelioma arising in the deltoid muscle without the Kasabach-Merritt phenomenon.

机构信息

Department of Orthopaedics, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.

出版信息

Skeletal Radiol. 2010 Oct;39(10):1043-6. doi: 10.1007/s00256-010-0917-1. Epub 2010 Mar 23.

Abstract

Kaposiform hemangioendothelioma (KHE) is a rare tumor that occurs nearly exclusively during infancy and childhood. It has features common to both capillary hemangioma and Kaposi sarcoma and for that reason many terms have been used for these tumors including "Kaposi-like infantile hemangioendothelioma" and "hemangioma with Kaposi sarcoma-like features." KHE typically presents as an ill-defined, red to purple, indurated plaque and is often complicated by the Kasabach-Merritt phenomenon (KMP), a condition of severe thrombocytopenia and consumptive coagulopathy. Knowledge of the radiological findings of this uncommon tumor might be helpful for diagnosis. We present the MRI features of a case of KHE with neither typical skin lesions nor the Kasabach-Merritt phenomenon.

摘要

卡波西样血管内皮细胞瘤(KHE)是一种罕见的肿瘤,几乎只发生在婴儿和儿童时期。它具有毛细血管血管瘤和卡波西肉瘤的共同特征,因此这些肿瘤有许多术语,包括“卡波西样婴儿血管内皮细胞瘤”和“具有卡波西肉瘤样特征的血管瘤”。KHE 通常表现为界限不清的红色至紫色硬结斑块,常伴有卡-梅现象(KMP),即严重血小板减少和消耗性凝血病。了解这种罕见肿瘤的放射学表现可能有助于诊断。我们报告了一例无典型皮肤病变和卡-梅现象的 KHE 的 MRI 特征。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验