Yeh Y C, Wu K H, Chi C S
Department of Pediatrics, Veterans General Hospital-Taichung, Taiwan, R.O.C.
Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1997 May-Jun;38(3):223-5.
Cutis marmorata telangiectatica congenita is an uncommon, congenital cutaneous lesion. It is usually present at birth, and is characterized by persistent fixed, flat, blue-violet cutaneous marmorata, telangiectasia, and phlebectasia. Frequently, there is associated skin atrophy and ulceration. There is an association with other abnormalities in at least 50% of the patients with cutis marmorata telangiectatica congenita. Thus, obtaining a thorough history and detailed physical examination are needed. We present a 38-day-old female infant with cutis marmorata telangiectatica congenita, with uneven growth of bilateral lower limbs, and review the literature on this rare lesion.
先天性大理石样皮肤毛细血管扩张症是一种罕见的先天性皮肤病变。它通常在出生时就存在，其特征为持续性固定的、扁平的、蓝紫色皮肤大理石样斑纹、毛细血管扩张和静脉扩张。通常还伴有皮肤萎缩和溃疡。至少50%的先天性大理石样皮肤毛细血管扩张症患者伴有其他异常。因此，需要全面的病史和详细的体格检查。我们报告一名38日龄患有先天性大理石样皮肤毛细血管扩张症且双侧下肢生长不均的女婴，并复习关于这种罕见病变的文献。
