Rapidly involuting congenital haemangioma in a term neonate

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Rapidly involuting congenital haemangioma in a term neonate.

To cite: Thoppay Kumarasamy M, Castrisios G, Sharma BK. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/ bcr-2013-203233 DESCRIPTION Following an uncomplicated pregnancy with normal antenatal scans, a term neonate was unexpectedly born with a large mass on the right temporal region (figure 1). This caused extreme anxiety among staff regarding the possibility of enceph...

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Rapidly involuting congenital hemangioma*

Rapidly involuting congenital hemangioma is a rare vascular tumor that generally has a good prognosis. The authors describe a case of a newborn girl with a left cervical vascular lesion. Image exams were performed, and the lesion slowly decreased, leaving redundant skin. Considering all of the findings, a final diagnosis of a rapidly involuting congenital hemangiomas was suspected.

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Rapidly involuting congenital hemangioma.

Volume 95 No. 5 May 2012 a newborn Male, delivered by Caesarean section after induction at 41 weeks of gestation for failure to progress, was admitted to the Women and Infants’ Hospital (WIH) Neonatal Intensive Care Unit (NICU) with a large vascular mass on his left knee (Figure 1). Routine prenatal US had been normal and the pregnancy had been uneventful. Physical examination at delivery was o...

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Rapidly Involuting Congenital Hemangioma of the Hand

Figure 1. Right hand with rapidly involuting congenital hemangioma.

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Congenital hemangiomas: rapidly involuting and noninvoluting congenital hemangiomas.

While infantile hemangiomas are a very common lesion seen in infants and young children, congenital hemangiomas are much more rare and have been only recently described. Two types of congenital hemangiomas exist: rapidly involuting congenital hemangiomas and noninvoluting congenital hemangiomas. The goal of this article is to describe rapidly involuting and noninvoluting congenital hemangiomas ...

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ژورنال

عنوان ژورنال: Case Reports

سال: 2014

ISSN: 1757-790X

DOI: 10.1136/bcr-2013-203233