PHACE syndrome - The association of posterior fossa brain malformations, hemangiomas, arterial anomalies, coarctation of the aorta and cardiac defects, and eye abnormalities

被引:434
作者
Frieden, IJ
Reese, V
Cohen, D
机构
[1] UNIV CALIF SAN FRANCISCO,DEPT PEDIAT,SAN FRANCISCO,CA 94143
[2] KAISER PERMANENTE MED CTR,DEPT PEDIAT,SAN JOSE,CA
关键词
D O I
10.1001/archderm.132.3.307
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: Large facial hemangiomas can have associated central nervous system malformations, particularly the Dandy-Walker posterior fossa malformations. Abnormal arteries, especially those of the central nervous system, coarctation of the aorta, cardiac defects,and unusual ophthalmologic abnormalities can also occur. Observations: We describe two patients with large facial hemangiomas, congenital cataracts, and structural arterial abnormalities, particularly of the central nervous system vasculature. One of these infants also had a Dandy-Walker malformation detected on prenatal ultrasound at 12 weeks' gestation, suggesting that this syndrome had its origin during the first trimester of pregnancy. This infant also had a Lingual thyroid and developed symptomatic hypothyroidism, possibly induced by interferon alfa therapy of her hemangioma. These cases are discussed, along with 41 previously reported cases with similar findings. Conclusions: Large facial hemangiomas may have a distinctive group of associated arterial, central nervous system, and ophthalmologic anomalies. We propose the acronym PHACE syndrome to emphasize the characteristic findings of this neurocutaneous syndrome: posterior fossa malformations, hemangiomas, arterial anomalies, coarctation of the aorta and cardiac defects, and eye abnormalities.
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页码:307 / 311
页数:5
相关论文
共 29 条
[1]   REVERSIBILITY OF THYROID-DYSFUNCTION INDUCED BY RECOMBINANT ALPHA-INTERFERON IN CHRONIC HEPATITIS-C [J].
BAUDIN, E ;
MARCELLIN, P ;
POUTEAU, M ;
COLASLINHART, N ;
LEFLOCH, JP ;
LEMMONIER, C ;
BENHAMOU, JP ;
BOK, B .
CLINICAL ENDOCRINOLOGY, 1993, 39 (06) :657-661
[2]   AN UNUSUAL CASE OF STURGE-WEBER SYNDROME [J].
BILLSON, VR ;
GILLAM, GL .
PATHOLOGY, 1984, 16 (04) :462-465
[3]  
BURNS AJ, 1991, PEDIATRICS, V88, P1257
[4]  
BURTON BK, 1993, PEDIATRICS, V91, P989
[5]   AN INCREASED INCIDENCE OF HEMANGIOMAS IN INFANTS BORN FOLLOWING CHORIONIC VILLUS SAMPLING (CVS) [J].
BURTON, BK ;
SCHULZ, CJ ;
ANGLE, B ;
BURD, LI .
PRENATAL DIAGNOSIS, 1995, 15 (03) :209-214
[6]  
CARMEL PW, 1977, SURG NEUROL, V8, P132
[7]  
CHUNG YH, 1993, AM J GASTROENTEROL, V88, P244
[8]  
Esterly N.B., 1995, CURR PROBL DERMATOL, V7, P69, DOI [10.1016/S1040-0486(09)80020-3, DOI 10.1016/S1040-0486(09)80020-3]
[9]   DIFFUSE NEONATAL HEMANGIOMATOSIS - A NEW CONSTELLATION OF FINDINGS [J].
GELLER, JD ;
TOPPER, SF ;
HASHIMOTO, K .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1991, 24 (05) :816-818
[10]  
GOH WHS, 1993, DEV MED CHILD NEUROL, V35, P631