Literature DB >> 20584448

PHACE Syndrome: Persistent Fetal Vascular Anomalies. A Case Report.

V Prochazka1, T Hrbac, J Chmelova, D Skoloudik, M Prochazka.   

Abstract

SUMMARY: PHACE(S) syndrome is an acronym for neurocutaneous disease encompassing the expression of (P) posterior cranial fossa malformations, (H) facial haemangiomas, (A) arterial anomalies, (C) aortic coarctaion and other cardiac defects, (E) eye abnormalities and (S) for sternal malformation or stenotic arterial diseases. We report on a case of PHACE syndrome complete expression with persistent fetal vascular anomalies unusually in a 55-year-old women with large bilateral facial and neck haemangioma and posterior fossa circulation insufficiency.

Entities:  

Year:  2006        PMID: 20584448      PMCID: PMC3399752          DOI: 10.1177/159101990501100408

Source DB:  PubMed          Journal:  Interv Neuroradiol        ISSN: 1591-0199            Impact factor:   1.610


  15 in total

Review 1.  The many faces of PHACE syndrome.

Authors:  D W Metry; C F Dowd; A J Barkovich; I J Frieden
Journal:  J Pediatr       Date:  2001-07       Impact factor: 4.406

2.  [Cutaneous hemangiomas, vascular malformations and associated disorders. A new neurocutaneous syndrome].

Authors:  I Pascual-Castroviejo; J C López-Gutiérrez; S I Pascual-Pascual; S Rafia; J Alarcón-Palacio
Journal:  An Pediatr (Barc)       Date:  2003-04       Impact factor: 1.500

3.  Posterior fossa and arterial abnormalities in patients with facial capillary haemangioma: presumed incomplete phenotypic expression of PHACES syndrome.

Authors:  A Rossi; G L Bava; R Biancheri; P Tortori-Donati
Journal:  Neuroradiology       Date:  2001-11       Impact factor: 2.804

4.  Hemangiomas and vascular malformations in infants and children: a classification based on endothelial characteristics.

Authors:  J B Mulliken; J Glowacki
Journal:  Plast Reconstr Surg       Date:  1982-03       Impact factor: 4.730

Review 5.  Ipsilateral hemangioma and aortic arch anomalies in posterior fossa malformations, hemangiomas, arterial anomalies, coarctation of the aorta, and cardiac defects and eye abnormalities (PHACE) anomaly: report and review.

Authors:  Gabriele Bronzetti; Alessandro Giardini; Annalisa Patrizi; Daniela Prandstraller; Andrea Donti; Roberto Formigari; Marco Bonvicini; Fernando Maria Picchio
Journal:  Pediatrics       Date:  2004-02       Impact factor: 7.124

6.  Report of a child with aortic aneurysm, orofacial clefting, hemangioma, upper sternal defect, and marfanoid features: possible PHACE syndrome.

Authors:  Anne M Slavotinek; Elizabeth Dubovsky; Harry C Dietz; Felicitas Lacbawan
Journal:  Am J Med Genet       Date:  2002-07-01

7.  Cervico-cerebrovascular anomalies in children with PHACE syndrome.

Authors:  Chao-Bao Luo; P Lasjaunias; Michael M H Teng; Feng Chi Chang; Jiing-Feng Lirng; Cheng-Yen Chang
Journal:  J Formos Med Assoc       Date:  2003-06       Impact factor: 3.282

8.  Cellular markers that distinguish the phases of hemangioma during infancy and childhood.

Authors:  K Takahashi; J B Mulliken; H P Kozakewich; R A Rogers; J Folkman; R A Ezekowitz
Journal:  J Clin Invest       Date:  1994-06       Impact factor: 14.808

9.  Facial hemangioma and malformation of the cortical development: a broadening of the PHACE spectrum or a new entity?

Authors:  S Grosso; L De Cosmo; E Bonifazi; P Galluzzi; M A Farnetani; P Loffredo; C Anichini; R Berardi; G Morgese; Paolo Balestri
Journal:  Am J Med Genet A       Date:  2004-01-15       Impact factor: 2.802

10.  PHACE syndrome: report of one case.

Authors:  Ming-Chih Lin; Chao-Huei Chen; Ching-Shiang Chi
Journal:  Acta Paediatr Taiwan       Date:  2003 Nov-Dec
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