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A Rare Case Report of Angiolymphoid Hyperplasia with Eosinophilia Arising in a Lipoma

机译:脂瘤引起的血管淋巴样增生伴嗜酸性粒细胞增多的罕见病例报告。

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Angiolymphoid Hyperplasia with Eosinophilia (ALHE) is a rare vascular disorder of controversial etiology, as to whether it is reactive or neoplastic. The usual site of occurrence is the head and neck area and sometimes in trunk and extremities. It is more commonly seen in women and in Asian population. We present a case of a 65 years old man who presented with a painless gradually increasing swelling in the interscapular region of the back which was diagnosed both clinically and on FNAC as a lipoma. Excision biopsy done subsequently revealed a benign lipomatous mass with variably sized firm grey white nodules showing histopathological features of ALHE in a lipoma. To the best of our knowledge, this is the first such case in literature of ALHE occurring in a lipoma which we are publishing for its unique presentation and morphology. Informed consent was taken from the patient prior to the procedure.
机译:嗜酸性粒细胞淋巴管增生(ALHE)是一种罕见的有争议的病因的血管疾病,无论是反应性的还是肿瘤性的。常见的发生部位是头部和颈部,有时在躯干和四肢。它在女性和亚洲人口中更为常见。我们介绍了一例65岁的男性患者,该患者在背部的肩inter骨间区域无痛性逐渐增大的肿胀,在临床上和FNAC上均被诊断为脂肪瘤。随后进行的切除活检显示良性脂肪瘤样肿块,大小不一的灰白色结节,显示脂肪瘤中ALHE的组织病理学特征。据我们所知,这是ALHE文献中首次出现在脂肪瘤中的病例,我们正以其独特的表现形式和形态对其进行发表。术前先征得患者的知情同意。

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