汲状血管内皮瘤:放射学难题

Abu Hanifah Ibrahim, K. A. Sayuti, Siti Nur Adni Mohd Ali, Noraziah Salehan
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引用次数: 0

摘要

卡波西泮状血管内皮瘤(KHE)是一种罕见的局部侵袭性血管肿瘤,确诊于婴儿期或儿童早期。与婴儿或先天性血管瘤相比,KHE 的预后较差,因为它具有浸润性,而且有可能发展成卡萨斯巴赫-梅里特综合征(KMS)。本病例报告的是一名 4 个月大的女孩,她出现了进行性左颈部肿胀。她被诊断为 KHE 和血小板减少症,提示为卡萨巴赫-梅里特综合征(KMS)。我们描述了 KHE 在超声波和磁共振成像上的表现。我们还强调了结合患者的临床病史、体格检查、实验室检查和影像学检查结果进行早期诊断的重要性,以预防与疾病相关的危及生命的并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Kaposiform haemangioendothelioma: A radiological dilemma
Kaposiform haemangioendothelioma (KHE) is a rare, locally aggressive vascular tumours diagnosed in infancy or early childhood. KHE has a worse prognosis than infantile or congenital haemangioma due to its infiltrative nature and risk of developing Kasabach-Merritt Syndrome (KMS). This case report is about a 4-month-old girl who presented with progressive left neck swelling. She was diagnosed with KHE and thrombocytopenia suggestive of Kasabach-Merritt Syndrome (KMS). We describe the imaging appearance of KHE on ultrasound and magnetic resonance imaging. We also highlight the importance of integrating patient’s clinical history with the physical, laboratory and imaging findings for early diagnosis to prevent disease-related life-threatening complications.  
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