Amin Ashima, Umashankar T, Dsouza Chryselle Olive
Assistant Professor, Department of Pathology, Father Muller Medical College and Hospita , Kankanady, Mangalore, Karnataka, India .
Professor, Department of Pathology, Father Muller Medical College and Hospital , Kankanady, Mangalore, Karnataka, India .
J Clin Diagn Res. 2015 Aug;9(8):ED16-7. doi: 10.7860/JCDR/2015/13044.6327. Epub 2015 Aug 1.
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.
嗜酸性粒细胞增多性血管淋巴样增生（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皮肤和皮下无痛性结节。中等大小的外周肌动脉受累并不常见。它主要影响三四十岁的白种成年人，但在亚洲人也有发生，在儿童中则极为罕见。我们在此报告一例46岁女性的血管内ALHE病例，该患者表现为前臂皮下结节，临床诊断为尺动脉血栓形成。
