Chessa Ricotti G, De Bernardi A, Corti P, Tofani S
Nuovo Ospedale San Giovanni di Dio, U.S.L. 10/C, Firenze, Italia.
Pediatr Med Chir. 1990 May-Jun;12(3):285-7.
We report two cases of C.M.T.C., a rare cutaneous vascular anomaly, which is manifested at birth. It is a rare birth defect of unknown etiology; usually occurs sporadically. There is an association of C.M.T.C. with other congenital anomalies in at least 50% of the patients. On the basis of two cases, the clinical features of cutis marmorata telangiectasica congenita are described and the differential diagnosis discussed.
我们报告了两例先天性大理石样皮肤血管扩张症（C.M.T.C.），这是一种罕见的皮肤血管异常，出生时即有表现。它是一种病因不明的罕见出生缺陷；通常为散发性。至少50%的患者中，先天性大理石样皮肤血管扩张症与其他先天性异常有关。基于这两例病例，描述了先天性大理石样皮肤血管扩张症的临床特征并讨论了鉴别诊断。
