Suppr超能文献

[进行性获得性淋巴管瘤:1例报告并文献复习]

[Progressive acquired lymphangioma: report of a case and review of the literature].

作者信息

Paredes Esteban R M, Velasco Sánchez B, Martínez-Victoria Muñoz J M, Cuevas C, García Ruiz M

机构信息

Sección de Cirugía Pediátrica, H.G.E. Ciudad de Jaén, Jaén.

出版信息

Cir Pediatr. 2000 Oct;13(4):170-1.

Abstract

We present 2-year-old patient with a allopecia lesions in scalp, and clinique diagnostic of Cutis Aplasia. The anatomopathologic study have diagnosed the lesions as Acquired Progressive Lymphangioma (APL). Is a rare vascular tumour that has a tendency to appear in childhood an to progress slowly over the years. It could present as a solitary erythematous macule or plaque and a simple excision is usually curative. Our patient is the youngest reported in the literature.

摘要

我们报告了一名2岁头皮有脱发病变的患者,临床诊断为皮肤发育不全。组织病理学研究将病变诊断为获得性进行性淋巴管瘤(APL)。这是一种罕见的血管肿瘤,倾向于在儿童期出现,并在多年内缓慢进展。它可表现为孤立的红斑或斑块,通常单纯切除即可治愈。我们的患者是文献报道中最年轻的。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验