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Angiolymphoid hyperplasia with eosinophilia occurring in bilateral eyelids

机译:双侧眼睑发生血管淋巴增生伴嗜酸性粒细胞增多

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Background Angiolymphoid hyperplasia with eosinophilia (ALHE) is an uncommon benign lesion, primarily occurring in the head and neck. ALHE arising from the ocular adnexa is rare, and the bilateral presentation is especially rare in the eyelids. Case presentation A 64-year-old Japanese man presented with tearing. Multiple nodules, approximately 5 mm in size, were observed in bilateral upper and lower eyelids. Surgical excisions of the both eyelids masses were performed. Histopathological examination of the excised masses demonstrated proliferated blood vessels lined by plump endothelial cells together with a lymphoid and eosinopilic infiltrate, compatible with a diagnosis of ALHE. Flow cytometry studies showed that the mass consisted of mostly CD3-positive cells. During two-year follow-up, no recurrence of the mass was observed and the patient had no subjective symptom of tearing Conclusion ALHE may occur in the bilateral eyelids. The cause of ALHE remains uncertain, but our results of flow cytemetry suggest that T cells are related to the pathogenesis of this disease.
机译:背景嗜酸性粒细胞增多症(ALHE)的血管淋巴样增生是一种罕见的良性病变,主要发生在头部和颈部。由眼附属物引起的ALHE很少见,双侧表现在眼睑中尤为罕见。案例介绍一名64岁的日本男子流泪。在双侧上眼睑和下眼睑观察到多个结节,大小约为5毫米。手术切除双眼皮肿块。切除的肿块的组织病理学检查显示,血管增生,内衬着丰满的内皮细胞,淋巴样和嗜酸细胞浸润,与ALHE的诊断相符。流式细胞术研究表明,肿块主要由CD3阳性细胞组成。在两年的随访中,未见肿块复发,患者无主观撕裂症状。结论ALHE可能在双眼皮中发生。 ALHE的病因仍不确定,但我们的流式细胞仪结果表明T细胞与该疾病的发病机制有关。

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