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CASE REPORT
Preoperative administration of propranolol reduced the surgical risks of PHACES syndrome in a 14-month-old girl
  1. Yuka Rokugo,
  2. Chiharu Ota,
  3. Masato Kimura and
  4. Yoji Sasahara
  1. Department of Pediatrics, Tohoku University School of Medicine, Sendai, Miyagi, Japan
  1. Correspondence to Dr Chiharu Ota, chipaota{at}gmail.com

Abstract

PHACES syndrome is an uncommon neurocutaneous disorder first identified in 1996. Patients with PHACES syndrome often require surgical treatment for their anomalies, including intracranial vasculopathy, coarctation/interruption of the aorta, intracardiac defects, glaucoma/cataract and sternal defects. Risk factors associated with the symptoms of intraoperative/perioperative management include ischaemic stroke due to the cerebral vasculopathy, airway obstruction due to the subglottic/tracheal haemangiomas and massive bleeding due to the large haemangiomas. Recently, propranolol is considered as first-line therapy for patients with infantile haemangiomas (IHs). However, until now, there have been no reported cases of PHACES syndrome treated by propranolol to reduce the surgical risks associated with IH. In this report, we describe a case of a 14-month-old Japanese girl with PHACES syndrome treated by propranolol for IH before surgical closure of the ventricular septum defect. Oral administration of propranolol was effective in decreasing the size of IH, leading to the uneventful perioperative course.

  • paediatrics
  • congenital disorders

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Footnotes

  • Contributors YR wrote the manuscript and collected the data. CO designed and edited the manuscript. MK edited the manuscript. YS served as a scientific adviser.

  • Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.

  • Competing interests None declared.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Patient consent for publication Parental/guardian consent obtained.