Ergon Ezgi Yangın, Çelik Kıymet, Çolak Rüya, Özdemir Senem Alkan, Olukman Özgür, Kundak Selcen, Çalkavur Şebnem
Department of Neonatology, İzmir Dr. Behçet Uz Children's Hospital, İzmir, Turkey.
Department of Dermatology, İzmir Dr. Behçet Uz Children's Hospital, İzmir, Turkey.
Turk Pediatri Ars. 2019 Jul 11;54(2):133-136. doi: 10.5152/TurkPediatriArs.2018.5557. eCollection 2019.
Cutis marmorata telangiectatica congenita is a rare, benign, sporadic and cutaneous vascular disease. A newborn female baby whose mother was aged 29 years and used propylthiouracil during pregnancy was hospitalized because of varicose lesions on the skin of the lower extremity and on the back, which were present at birth. It was observed that the lesions did not disappear, although appropriate room temperature was provided. The patient was diagnosed as having cutis marmorata telangiectatica congenita and screened for additional anomalies. She had no additional anomalies, and she was discharged and monitored. At the postnatal sixth month, the cutaneous vascular lesions disappeared spontaneously. Cutis marmorata telangiectatica congenita, which is a rare condition, should be kept in mind in the differential diagnosis of physiologic cutis marmoratus, which occurs frequently in the neonatal period.
先天性大理石样皮肤毛细血管扩张症是一种罕见的、良性的、散发性的皮肤血管疾病。一名母亲29岁、孕期使用丙硫氧嘧啶的新生女婴因出生时即存在的下肢及背部皮肤静脉曲张性病变入院。尽管提供了适宜的室温，但发现病变并未消失。该患者被诊断为先天性大理石样皮肤毛细血管扩张症，并接受了其他异常情况的筛查。她没有其他异常情况，随后出院并接受监测。出生后第六个月，皮肤血管病变自行消失。先天性大理石样皮肤毛细血管扩张症这种罕见病症，在新生儿期常见的生理性大理石样皮肤的鉴别诊断中应予以考虑。
