Recurrent intravascular papillary endothelial hyperplasia developing from a pyogenic granuloma
Recurrent intravascular papillary endothelial hyperplasia developing from a pyogenic granuloma
复制标题
由化脓性肉芽肿发展而来的复发性血管内乳头状内皮增生
DOI：
10.1046/j.1468-3083.2001.00228.x
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发表时间：
2001
影响因子：
9.2
通讯作者：
Ag Knight
中科院分区：
文献类型：
--
作者：
H. Inalöz;G. Patel;Ag Knight
血管内乳头状内皮增生是一种罕见的良性血管肿瘤。许多组织学特征与低度恶性血管肉瘤相似，低度恶性血管肉瘤是一种常见但更严重的疾病。临床和组织学分化是重要的，以避免过度治疗这种良性疾病。我们报告了一名34岁的女性，她在先前切除的化脓性肉芽肿部位发生了复发性IPEH。
Intravascular papillary endothelial hyperplasia (IPEH) is a rare benign vascular tumour. Many histological features are similar to those of low‐grade angiosarcoma, a common, but more serious condition. Clinical and histological differentiation is important to avoid overtreatment of this benign condition. We report on a 34‐year‐old woman who developed recurrent IPEH at the site of a previously excised pyogenic granuloma.