Aorto-pulmonary calcification: An unusual manifestation of idiopathic calcification of infancy evident antenatally

Lindy M. Samson, Karen M. Ash, Kenneth A. Murdison

Research output: Contribution to journalArticle

28 Scopus citations

Abstract

Background: Idiopathic arterial calcification of infancy represents a clinical spectrum involving calcification of large and medium-sized blood vessels with an unknown etiology. Its complications include severe systemic hypertension and cardiomyopathy. Case: A twin infant with a variant of idiopathic arterial calcification was diagnosed antenatally by the detection of hyperechogenicity of the proximal aorta and central pulmonary vessels. The calcification was apparently isolated to these vessels and was associated with polyhydramnios and hypertrophic cardiomyopathy. Conclusion: Because antenatal diagnosis is possible, we suggest that there should be a high index of suspicion for idiopathic arterial calcification when there is sonographic hyperechogenicity of vessel walls, evidence of polyhydramnios, cardiomyopathy, or a family history of idiopathic arterial calcification.

Original languageEnglish (US)
Pages (from-to)863-865
Number of pages3
JournalObstetrics and gynecology
Volume85
Issue number5
DOIs
StatePublished - Jan 1 1995
Externally publishedYes

ASJC Scopus subject areas

  • Obstetrics and Gynecology

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