PHACE syndrome with parotid hemangiomas: a unique case report

Abstract Background PHACE syndrome is a congenital disorder in infants characterized by the presence of large hemangiomas in the cervicofacial region along with congenital anomalies of the cardiovascular system, brain, and eyes. PHACE syndrome is an extremely rare condition, and PHACE syndrome with...

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Main Authors: Muhammad Umer Mukhtar, Mahjabeen Kanwal, Adeel Qamar, Sadaf Arooj, Samina Qamar
Format: Article
Language:English
Published: SpringerOpen 2021-01-01
Series:The Egyptian Journal of Radiology and Nuclear Medicine
Subjects:
Online Access:https://doi.org/10.1186/s43055-020-00387-9
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spelling doaj-3b506de070de4156a1cfb34e1d4fb7172021-01-10T12:50:55ZengSpringerOpenThe Egyptian Journal of Radiology and Nuclear Medicine2090-47622021-01-015211410.1186/s43055-020-00387-9PHACE syndrome with parotid hemangiomas: a unique case reportMuhammad Umer Mukhtar0Mahjabeen Kanwal1Adeel Qamar2Sadaf Arooj3Samina Qamar4King Edward Medical UniversityDepartment of Radiology, King Edward Medical UniversityDepartment of Radiology, King Edward Medical UniversityDepartment of Radiology, King Edward Medical UniversityDepartment of Pathology, King Edward Medical UniversityAbstract Background PHACE syndrome is a congenital disorder in infants characterized by the presence of large hemangiomas in the cervicofacial region along with congenital anomalies of the cardiovascular system, brain, and eyes. PHACE syndrome is an extremely rare condition, and PHACE syndrome with parotid hemangiomas has never been reported in the medical literature. Case presentation A 3-month-old female infant presented with cervicofacial plaques that later involved the left eyelids. The plaques blanched on application of pressure and were diagnosed to be hemangiomas. MRI and MRA studies of the brain showed extensive vascular malformations, agenesis of the left internal carotid artery, and hemangiomas in the parotid glands. A biopsy of the parotid glands confirmed the parotid hemangiomas. Bilateral cataracts and subclavian artery with an aberrant origin were also found. On the basis of the hemangiomas and the arterial, cardiovascular, and ocular abnormalities, PHACE syndrome was diagnosed. A multi-disciplinary treatment approach was begun, but the infant died 20 days after presentation to the hospital. Conclusions PHACE syndrome is an extremely rare condition that has only been described three hundred times in medical literature. It is usually associated with extensive structural, arterial, ocular, and cutaneous anomalies. However, PHACE syndrome with parotid hemangiomas has never been reported in the medical literature. Hemangiomas are the main diagnostic feature and the most common lesion of this disease. This strong association between PHACE syndrome and hemangiomas suggests the parotid hemangiomas seen in our case to be a new addition to the broad spectrum of anomalies associated with PHACE syndrome.https://doi.org/10.1186/s43055-020-00387-9PHACE syndromeInfantile hemangiomaVascular anomaliesEye abnormalitiesMagnetic resonance imagingCase report
collection DOAJ
language English
format Article
sources DOAJ
author Muhammad Umer Mukhtar
Mahjabeen Kanwal
Adeel Qamar
Sadaf Arooj
Samina Qamar
spellingShingle Muhammad Umer Mukhtar
Mahjabeen Kanwal
Adeel Qamar
Sadaf Arooj
Samina Qamar
PHACE syndrome with parotid hemangiomas: a unique case report
The Egyptian Journal of Radiology and Nuclear Medicine
PHACE syndrome
Infantile hemangioma
Vascular anomalies
Eye abnormalities
Magnetic resonance imaging
Case report
author_facet Muhammad Umer Mukhtar
Mahjabeen Kanwal
Adeel Qamar
Sadaf Arooj
Samina Qamar
author_sort Muhammad Umer Mukhtar
title PHACE syndrome with parotid hemangiomas: a unique case report
title_short PHACE syndrome with parotid hemangiomas: a unique case report
title_full PHACE syndrome with parotid hemangiomas: a unique case report
title_fullStr PHACE syndrome with parotid hemangiomas: a unique case report
title_full_unstemmed PHACE syndrome with parotid hemangiomas: a unique case report
title_sort phace syndrome with parotid hemangiomas: a unique case report
publisher SpringerOpen
series The Egyptian Journal of Radiology and Nuclear Medicine
issn 2090-4762
publishDate 2021-01-01
description Abstract Background PHACE syndrome is a congenital disorder in infants characterized by the presence of large hemangiomas in the cervicofacial region along with congenital anomalies of the cardiovascular system, brain, and eyes. PHACE syndrome is an extremely rare condition, and PHACE syndrome with parotid hemangiomas has never been reported in the medical literature. Case presentation A 3-month-old female infant presented with cervicofacial plaques that later involved the left eyelids. The plaques blanched on application of pressure and were diagnosed to be hemangiomas. MRI and MRA studies of the brain showed extensive vascular malformations, agenesis of the left internal carotid artery, and hemangiomas in the parotid glands. A biopsy of the parotid glands confirmed the parotid hemangiomas. Bilateral cataracts and subclavian artery with an aberrant origin were also found. On the basis of the hemangiomas and the arterial, cardiovascular, and ocular abnormalities, PHACE syndrome was diagnosed. A multi-disciplinary treatment approach was begun, but the infant died 20 days after presentation to the hospital. Conclusions PHACE syndrome is an extremely rare condition that has only been described three hundred times in medical literature. It is usually associated with extensive structural, arterial, ocular, and cutaneous anomalies. However, PHACE syndrome with parotid hemangiomas has never been reported in the medical literature. Hemangiomas are the main diagnostic feature and the most common lesion of this disease. This strong association between PHACE syndrome and hemangiomas suggests the parotid hemangiomas seen in our case to be a new addition to the broad spectrum of anomalies associated with PHACE syndrome.
topic PHACE syndrome
Infantile hemangioma
Vascular anomalies
Eye abnormalities
Magnetic resonance imaging
Case report
url https://doi.org/10.1186/s43055-020-00387-9
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