伴有双上腔静脉、腹部静脉曲张和诞生牙的2b型色素血管性母斑病（焰色母斑病）：新的关联。
Phacomatosis pigmentovascularis type 2b (phacomatosis cesioflammea) with double superior vena cava, abdominal varicosities, and natal tooth: Novel associations.
作者信息
Singal Archana, Mittal Hema, Aggarwal Anju, Das Saurabhi, Manchanda Smita
机构信息
Department of Dermatology and Sexually Transmitted Diseases, University College of Medical Sciences & GTB Hospital, University of Delhi, New Delhi, India.
Department of Pediatrics, Dr. RML Hospital and Postgraduate Institute of Medical Education and Research, New Delhi, India.
出版信息
Pediatr Dermatol. 2018 May;35(3):e151-e154. doi: 10.1111/pde.13427. Epub 2018 Feb 26.
Phacomatosis pigmentovascularis is characterized by coexistent extensive cutaneous vascular (capillary) and pigmentary anomalies. We describe a 2-month-old infant presenting with classic features of phacomatosis pigmentovascularis 2b (phacomatosis cesioflammea). He was also found to have hitherto unreported associations in the form of extensive venous anomalies presenting as striking abdominal wall varicosities and persistent left superior vena cava and natal tooth.
色素血管性斑痣性错构瘤病的特征是广泛的皮肤血管（毛细血管）和色素异常并存。我们描述了一名2个月大的婴儿，具有色素血管性斑痣性错构瘤病2b型（焰色痣样错构瘤病）的典型特征。他还被发现有一些此前未报道的关联情况，表现为广泛的静脉异常，如显著的腹壁静脉曲张、永存左上腔静脉和诞生牙。
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