上颚血管淋巴样增生伴嗜酸性粒细胞增多1例并文献复习

Pooja Medikonda, Satyanarayana Akula, R. Manyam, P. Swetha, K. Moturi, R. Tatapudi
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引用次数: 0

摘要

血管淋巴样增生伴组织嗜酸性粒细胞增多症(ALHE)是一种罕见的良性血管肿瘤,病因不明,最常见于头颈部。临床上通常表现为棕色或紫色丘疹或结节,主要见于女性。顾名思义,组织学上表现为内皮细胞增生和淋巴细胞聚集,伴间质嗜酸性粒细胞增多。它在临床上很少被发现,诊断纯粹是基于组织病理学。这是一个独特的病例报告,口腔内ALHE具有不寻常的临床表现为溃疡增生性病变,在切口活检后表现出快速缓解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Angiolymphoid hyperplasia with eosinophilia of the palate: A case report with literature review
Angiolymphoid hyperplasia with tissue eosinophilia (ALHE) is a rarely occurring benign vascular tumor of unknown etiology and most commonly affecting the head and neck region. It usually presents clinically as brownish or purplish papules or nodules with major prevalence in females. As the name defines, histologically it shows proliferating endothelial cells and lymphoid aggregates with stromal eosinophilia. It is very rarely identified clinically and the diagnosis is purely based on histopathology. This is a unique case report of intraoral ALHE with an unusual clinical appearance as ulceroproliferative lesion that showed quick remission after incisional biopsy.
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