Update on hemangiomas and vascular malformations.

Hemangiomas and vascular malformations are frequently encountered in pediatric practice, especially hemangiomas and port-wine stains. These lesions may cause physical and psychological complications and it is important to recognize which lesions need to be treated and how. Great progress has been made in the classification of vascular anomalies. Angiogenesis and molecular genetics are areas of active research; recent findings relating to hemangiomas and vascular malformations are presented. New clinical features of hemangiomas are described, such as association of extensive facial hemangiomas with various malformations and the occurrence of Kasabach-Merritt phenomenon, not with common hemangiomas, but with other vascular tumors (Kaposiform hemangioendothelioma and tufted angioma). Interferon alfa is effective for treatment of complicated hemangiomas but may cause serious neurological side effects. It is to be hoped that early diagnosis of Sturge-Weber syndrome will soon be possible with new, noninvasive, functional imaging techniques. New issues surrounding pulsed dye laser therapy for port-wine stains are also discussed in this article.

[1]  J. Mulliken,et al.  Molecular basis of vascular anomalies. , 1998, Trends in cardiovascular medicine.

[2]  R. Robertson,et al.  Diagnostic imaging in the evaluation of vascular birthmarks. , 1998, Dermatologic clinics.

[3]  A. Troilius,et al.  Potential psychological benefits from early treatment of port‐wine stains in children , 1998, The British journal of dermatology.

[4]  G. Moore,et al.  Proton Magnetic Resonance Spectroscopy in Children With Sturge-Weber Syndrome , 1998, Journal of child neurology.

[5]  L. Garel,et al.  Soft-tissue hemangiomas in infants and children: diagnosis using Doppler sonography. , 1998, AJR. American journal of roentgenology.

[6]  L. Eichenfield Evolving knowledge of hemangiomas and vascular malformations: beyond strawberries and port wine. , 1998, Archives of dermatology.

[7]  S. Orlow,et al.  Familial segregation of hemangiomas and vascular malformations as an autosomal dominant trait. , 1998, Archives of dermatology.

[8]  J. Mulliken,et al.  Cerebral vasculopathy and neurologic sequelae in infants with cervicofacial hemangioma: report of eight patients. , 1998, Radiology.

[9]  L. Garel,et al.  Imaging of hemangiomas and vascular malformations in children. , 1998, Academic radiology.

[10]  Huff,et al.  Facial port wine stains in childhood: prediction of the rate of improvement as a function of the age of the patient, size and location of the port wine stain and the number of treatments with the pulsed dye (585 nm) laser , 1998, The British journal of dermatology.

[11]  P. Bossuyt,et al.  Effect of the timing of treatment of port-wine stains with the flash-lamp-pumped pulsed-dye laser. , 1998, The New England journal of medicine.

[12]  J. Mulliken,et al.  Spastic diplegia as a complication of interferon Alfa-2a treatment of hemangiomas of infancy. , 1998, The Journal of pediatrics.

[13]  A. Barkovich,et al.  Sturge-Weber syndrome with no leptomeningeal enhancement on MRI , 1998, Neuroradiology.

[14]  M. Gniadecka,et al.  Changes in skin redness, pigmentation, echostructure, thickness, and surface contour after 1 pulsed dye laser treatment of port-wine stains in children. , 1998, Archives of dermatology.

[15]  F. Teixeira,et al.  Therapeutic efficacy of interferon alfa-2b in infants with life-threatening giant hemangiomas. , 1997, Archives of dermatology.

[16]  I. Frieden Which hemangiomas to treat--and how? , 1997, Archives of dermatology.

[17]  I. Frieden,et al.  Kaposiform hemangioendothelioma : An aggressive, locally invasive vascular tumor that can mimic hemangioma of infancy , 1997 .

[18]  O. Dulac,et al.  Early single photon emission computed tomography in Sturge-Weber syndrome , 1997, Journal of neurology, neurosurgery, and psychiatry.

[19]  J. Mulliken,et al.  Thrombocytopenic Coagulopathy (Kasabach‐Merritt Phenomenon) Is Associated with Kaposiform Hemangioendothelioma and Not with Common Infantile Hemangioma , 1997, Plastic and reconstructive surgery.

[20]  S. Orlow,et al.  Increased risk of symptomatic hemangiomas of the airway in association with cutaneous hemangiomas in a "beard" distribution. , 1997, The Journal of pediatrics.

[21]  B. Maria,et al.  Central Nervous System Perfusion and Metabolism Abnormalities in Sturge-Weber Syndrome , 1997, Journal of child neurology.

[22]  A. Taïeb,et al.  Infants with Kasabach-Merritt syndrome do not have "true" hemangiomas. , 1997, The Journal of pediatrics.

[23]  P. Griffiths,et al.  99mTechnetium HMPAO imaging in children with the Sturge-Weber syndrome: a study of nine cases with CT and MRI correlation , 1997, Neuroradiology.

[24]  J. Arbiser Angiogenesis and the skin: a primer. , 1996, Journal of the American Academy of Dermatology.

[25]  I. Frieden,et al.  PHACE Syndrome: The Association of Posterior Fossa Brain Malformations, Hemangiomas, Arterial Anomalies, Coarctation of the Aorta and Cardiac Defects, and Eye Abnormalities , 1996 .

[26]  J. Folkman Clinical Applications of Research on Angiogenesis , 1995 .

[27]  N. Esterly Cutaneous hemangiomas, vascular stains and malformations, and associated syndromes , 1995 .

[28]  J. Mulliken,et al.  Cellular markers that distinguish the phases of hemangioma during infancy and childhood. , 1994, The Journal of clinical investigation.

[29]  D. Young,et al.  Kasabach-Merritt syndrome. , 1988, Journal of pediatric surgery.

[30]  J. Glowacki,et al.  Hemangiomas and Vascular Malformations in Infants and Children: A Classification Based on Endothelial Characteristics , 1982, Plastic and reconstructive surgery.

[31]  K. Merritt,et al.  CAPILLARY HEMANGIOMA WITH EXTENSIVE PURPURA: REPORT OF A CASE , 1940 .

[32]  S. Orlow,et al.  Genetic mapping of a novel familial form of infantile hemangioma. , 1999, American journal of medical genetics.

[33]  N. Bauman,et al.  An update on the treatment of hemangiomas in children with interferon alfa-2a. , 1999, Archives of otolaryngology--head & neck surgery.