Gupta Aastha, Sardana Kabir, Arora Pooja, Garga Umesh C, Malhotra Purnima
Department of Dermatology, PGIMER Dr Ram Manohar Lohia Hospital, New Delhi, India.
Department of Radiology, PGIMER Dr Ram Manohar Lohia Hospital, New Delhi, India.
Pediatr Dermatol. 2019 Nov;36(6):967-969. doi: 10.1111/pde.13961. Epub 2019 Aug 25.
A 3-year-old boy presented to us with swelling of the right upper lip and the surrounding perioral area with the multiple clear fluid-filled grouped vesicles on the mucosal surface. The patient's mother had a similar swelling located at the same anatomic location extending to the cheek and the ala of nose on the same side. Magnetic resonance imaging and histopathological examination were suggestive of microcystic lymphatic malformation (LM) in both mother and child. Although an autosomal recessive inheritance pattern has been reported for isolated cystic hygromas, no familial case of microcystic LM has been reported previously.
一名3岁男孩前来就诊,其右上唇及口周区域肿胀,黏膜表面有多个清亮液性成簇水疱。患儿母亲在相同解剖部位有类似肿胀,延伸至同侧脸颊和鼻翼。磁共振成像和组织病理学检查提示母婴均为微囊型淋巴管畸形(LM)。虽然孤立性囊状水瘤有常染色体隐性遗传模式的报道,但此前尚无微囊型LM的家族病例报告。