Paredes Esteban R M, Velasco Sánchez B, Martínez-Victoria Muñoz J M, Cuevas C, García Ruiz M
Sección de Cirugía Pediátrica, H.G.E. Ciudad de Jaén, Jaén.
Cir Pediatr. 2000 Oct;13(4):170-1.
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.
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。