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A case of congenital hypothyroidism in PHACE syndrome

Authors :
Nadia Vercellino
Silvia Carinci
Alessia Di Stefano
Pietro Dalmonte
N.P. Consilvio
Stefano Tumini
Francesco Chiarelli
Paola Cipriano
Source :
Journal of pediatric endocrinologymetabolism : JPEM. 25(5-6)
Publication Year :
2012

Abstract

Although hemangiomas, benign tumors of vascular origin, are very common among children and represent the most frequent benign tumor at that age, their association with other malformations constitutes a rare neurocutaneous disorder called PHACE syndrome. This condition is characterized by posterior fossa anomalies, hemangioma of the face, arterial alterations, cardiac defects, and eye anomalies (as represented by the acronym PHACE); sternum defects, endocrinopathies, and thyreopathies may be present as well. In this report, we describe a case of congenital hypothyroidism due to an empty thyroid site, as demonstrated by ultrasound, in an Italian child.

Details

ISSN :
0334018X
Volume :
25
Issue :
5-6
Database :
OpenAIRE
Journal :
Journal of pediatric endocrinologymetabolism : JPEM
Accession number :
edsair.doi.dedup.....337be491c7294ca5c768b1c48e0b1cc4