成人单侧血管发育不全的罕见病例-晚期诊断为PHACE综合征

IF 0.8 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS International journal of cardiology. Congenital heart disease Pub Date : 2023-09-01 DOI:10.1016/j.ijcchd.2023.100465
Madelien V. Regeer , J. Lauran Stöger , Regina Bökenkamp , Inge M.M. Lakeman , Mark G. Hazekamp , Philippine Kiѐs , Anastasia D. Egorova , Monique R.M. Jongbloed
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引用次数: 0

摘要

本文报告一例单侧血管发育不全。一位女性患者出生时主动脉弓解剖结构复杂-双主动脉弓和左主动脉弓中断。3个月时进行手术矫正。患者还被注意到有一个大的同侧婴儿血管瘤。这些发现提高了对PHACE综合征诊断的怀疑。PHACE综合征是后颅窝异常、血管瘤、动脉异常、心脏异常和眼睛异常的首字母缩略词。未来的研究需要阐明PHACE综合征的潜在病理生理机制。
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An unusual case of unilateral vascular hypoplasia in an adult patient – late diagnosis of PHACE syndrome

A case of unilateral vascular hypoplasia is presented. A female patient was born with a complex aortic arch anatomy - a double aortic arch with an interrupted left arch. Surgical correction was performed at the age of 3 months. The patient was also noted to have had an ipsilateral large infantile haemangioma. These findings raised the suspicion of the diagnosis of PHACE syndrome. PHACE syndrome is an acronym for Posterior fossa abnormalities, Haemangioma, Arterial anomalies, Cardiac anomalies and Eye anomalies. Future research is needed to elucidate the underlying pathophysiology in PHACE syndrome.

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来源期刊
International journal of cardiology. Congenital heart disease
International journal of cardiology. Congenital heart disease Cardiology and Cardiovascular Medicine
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