Iznardo Helena, Baselga Eulalia, Mozos Anna, Szafranska Justyna, Orellana-Fernández Ruth, Roé Esther
Department of Dermatology, Hospital de la Santa Creu i Sant Pau, Universitat Autònoma de Barcelona, Barcelona, Spain.
Department of Dermatology, Hospital Sant Joan de Déu, Esplugues de Llobregat, Barcelona, Spain.
Pediatr Dermatol. 2021 Mar;38(2):516-517. doi: 10.1111/pde.14526. Epub 2021 Jan 24.
The net-like superficial lymphatic malformation (LM) is a newly described entity with distinctive clinical, dermoscopic, and histologic characteristics. Clinical picture consists of red to purplish macules with a finely reticulated pattern of vascular structures. Dermoscopy shows arborizing telangiectatic vessels. Histology is characterized by a vascular proliferation composed of thin-walled vessels, located in the upper dermis, that stains positive with podoplanin (D2-40). We report a new case of LM with an additional clinical feature, hypopigmented areas.
网状浅表淋巴管畸形(LM)是一种新描述的疾病,具有独特的临床、皮肤镜和组织学特征。临床表现为红色至紫色斑疹,伴有血管结构的精细网状图案。皮肤镜显示树枝状扩张的毛细血管。组织学特征为位于真皮上层的由薄壁血管组成的血管增生,对足突蛋白(D2-40)染色呈阳性。我们报告一例具有额外临床特征——色素减退区域的LM新病例。