Picascia D D, Esterly N B
Department of Dermatology, Northwestern University Medical School, Chicago.
J Am Acad Dermatol. 1989 Jun;20(6):1098-1104. doi: 10.1016/s0190-9622(89)70140-7.
Twenty-two cases of cutis marmorata telangiectatica congenita were evaluated during an 8-year period. All but two patients were examined in the first year of life; 14 of the 22 (64%) were female infants. Four patients had focal cutaneous atrophy associated with the reticulated vascular pattern, and eight had ulcerations of involved skin. Six (27%) had additional anomalies. Of these, three patients had a nevus flammeus, and one had congenital generalized fibromatosis and hemiatrophy. Two of the infants had glaucoma; one also had a facial nevus flammeus and the other had cutis marmorata telangiectatica congenita of the face. A congenital pigmented nevus and a localized venous malformation constituted the remaining associated defects. This disease is an uncommon cutaneous vascular anomaly that is most often solitary but occasionally may be associated with other developmental defects.
在8年期间对22例先天性网状青斑样毛细血管扩张症患者进行了评估。除2例患者外,其余均在出生后第一年接受检查;22例中有14例(64%)为女婴。4例患者出现与网状血管形态相关的局限性皮肤萎缩,8例患者受累皮肤出现溃疡。6例(27%)有其他异常。其中,3例患者有鲜红斑痣,1例有先天性全身性纤维瘤病和半侧萎缩。2例婴儿患有青光眼;1例还伴有面部鲜红斑痣,另1例面部患有先天性网状青斑样毛细血管扩张症。其余相关缺陷包括先天性色素痣和局限性静脉畸形。本病是一种罕见的皮肤血管异常,多数情况下为单发,但偶尔可能与其他发育缺陷相关。