儿童罕见肿瘤自发性消退:血管淋巴样增生伴手部嗜酸性粒细胞增多:病例报告及文献复习

A. Satpathy , C. Moss , F. Raafat , R. Slator
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引用次数: 48

摘要

血管淋巴样增生伴嗜酸性粒细胞增多症(ALHE)是一种罕见的良性特发性血管增生性疾病,表现为多发或单发皮下结节,通常发生在年轻人的头颈部。这在四肢尤其是手部非常罕见。虽然复发是常见的,手术切除仍然被认为是治疗的选择。我们报告一个11岁的女孩,组织学证实她的左手背ALHE,在10周内完全自发消退。血管淋巴样增生是一种良性疾病,重要的是要认识到这种情况,以便早期的浅表病变可以观察3-6个月,直到自发消退。
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Spontaneous regression of a rare tumour in a child: angiolymphoid hyperplasia with eosinophilia of the hand: case report and review of the literature

Angiolymphoid hyperplasia with eosinophilia (ALHE) is an uncommon benign, idipathic vasculoproliferative condition manifested by multiple or solitary subcutaneous nodules, usually in the head and neck region of young adults. It is very rare in the extremities especially in the hands. Although recurrence is common, surgical excision is still regarded as the treatment of choice. We report an 11-year-old girl with histologically confirmed ALHE on the dorsum of her left hand, which underwent complete spontaneous regression within 10 weeks. Angiolymphoid hyperplasia is a benign disease and it is important to recognise this condition so that early superficial lesions can be observed for 3–6 months pending spontaneous regression.

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