首页> 美国卫生研究院文献>Journal of Clinical and Diagnostic Research : JCDR >Intra-Arterial Angiolymphoid Hyperplasia with Eosinophilia: A Rare Case Report of Peripheral Medium Sized Muscular Artery Involvement
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Intra-Arterial Angiolymphoid Hyperplasia with Eosinophilia: A Rare Case Report of Peripheral Medium Sized Muscular Artery Involvement

机译:嗜酸性粒细胞增多的动脉内血管淋巴样增生:周围中型肌肉动脉受累的罕见病例报告

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摘要

Angiolymphoid hyperplasia with eosinophilia (ALHE) is an uncommon benign vasoproliferative disease with distinct clinical and histopathological features. The most common clinical presentation is dermal and subcutaneous painless nodules in the head and neck region. The involvement of medium sized peripheral muscular artery is uncommon. It predominantly affects Caucasian adults during the third and fourth decades, but is also known to occur in Asians and it very rarely occurs in children. We here by present a case of intravascular ALHE in a 46-year-old female presenting with subcutaneous forearm nodule clinically diagnosed as ulnar artery thrombosis.
机译:嗜酸性粒细胞增多的血管淋巴样增生(ALHE)是一种罕见的良性血管增生性疾病,具有独特的临床和组织病理学特征。最常见的临床表现是头颈部的真皮和皮下无痛结节。中型外周肌动脉受累并不常见。它主要在第三和第四十年影响白种人,但也已知发生在亚洲人中,很少发生在儿童中。我们在此介绍了一名46岁女性的血管内ALHE病例,该女性表现为临床被诊断为尺动脉血栓形成的皮下前臂结节。

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