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Angiogenesis

, Volume 12, Issue 2, pp 197–207 | Cite as

Vasculogenesis in infantile hemangioma

  • Elisa Boscolo
  • Joyce BischoffEmail author
Original Paper

Abstract

Infantile hemangioma is a vascular tumor that occurs in 5–10% of infants of European descent. A defining feature of infantile hemangioma is the dramatic growth and development into a disorganized mass of blood vessels. Subsequently, a slow spontaneous involution begins around 1 year of age and continues for 4–6 years. The growth and involution of infantile hemangioma is very different from other vascular tumors and vascular malformations, which do not regress and can occur at any time during childhood or adult life. Much has been learned from careful study of the tissue morphology and gene expression patterns during the life-cycle of hemangioma. Tissue explants and tumor-derived cell populations have provided further insight to unravel the cellular and molecular basis of infantile hemangioma. A multipotent progenitor cell capable of de novo blood vessel formation has been isolated from infantile hemangioma, which suggests that this common tumor of infancy, long considered to be a model for pathologic angiogenesis, may also represent pathologic vasculogenesis. Whether viewed as angiogenesis or vasculogenesis, infantile hemangioma represents a vascular perturbation during a critical period of post-natal growth, and as such provides a unique opportunity to decipher mechanisms of human vascular development.

Keywords

Angiogenesis Endothelial cells Endothelial progenitor cells Hemangioma Vasculogenesis VEGF-receptors 

Notes

Acknowledgments

We thank Dr. Arnaud Picard, Hôpital d’enfants Armand-Trousseau, Service de Chirurgie Maxillo-faciale et Plastique, Paris, France, for providing the images of the CD133 and NG2 immunostaining in Fig. 2. We also thank Ms. Kristin Johnson for her help with preparing the figures. Writing of this article was supported by a grant from the National Institutes of Health (P01 AR48564).

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© Springer Science+Business Media B.V. 2009

Authors and Affiliations

  1. 1.Vascular Biology Program, Department of Surgery, Children’s Hospital Boston Harvard Medical SchoolBostonUSA

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