 |
 |

Port-wine StainsA Disease of Altered Neural Modulation of Blood Vessels?
Bruce R. Smoller, MD;
Seymour Rosen, MD
Arch Dermatol. 1986;122(2):177-179.
Abstract
 |  |
Port-wine stains result from a progressive ectasia of the cutaneous superficial vascular plexus. One hypothesis for the pathogenesis of this lesion is an abnormal neural regulation of blood flow. Biopsy specimens of 11 port-wine stains, seven hemangiomas, and 17 benign lesions were stained for S100 protein using immunoperoxidase techniques. All specimens were of facial biopsies or excisions and were evaluated for vessels per square millimeter, nerves per square millimeter, vesselto-nerve ratio, and frequency of vessels coursing within 0.03 mm of nerves. These variables were evaluated in the superficial 0.8 mm of dermis, a zone that includes almost all abnormal port-wine-stain vessels. Controls showed 18.3 ± 2.8 vessels/sq mm (±SD), 21.1 ± 9.2 nerves/sq mm, 0.9 ± 0.3 vessels to nerves, and 75% ± 11% of vessels coursing within 0.03 mm of nerves, values that did not alter with age. Port-wine stains had a significant decrease in nerve density and increase in vessel-to-nerve ratio when compared with normal skin; only 17% ± 3% of vessels were associated with nerves in port-wine stains. These findings document a deficit in the number of perivascular nerves in port-wine stains and raise the possibility that a lack of neural modulation of vascular flow may be involved in the pathogenesis of port-wine stains.
(Arch Dermatol 1986;122:177-179)
Author Affiliations
From the Department of Pathology, Beth Israel Hospital and Harvard Medical School and the Charles A. Dana Institute, Boston.
Footnotes
Accepted for publication Nov 20, 1985.
Reprint requests to Department of Pathology, Beth Israel Hospital, 330 Brookline Ave, Boston, MA 02215 (Dr Rosen).
CiteULike Connotea Del.icio.us Digg Reddit Technorati Twitter
What's this?
THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES
 |
Genetic causes of vascular malformations
Brouillard and Vikkula
Hum Mol Genet 2007;16:R140-R149.
ABSTRACT
| FULL TEXT
Bilateral facial capillary malformation associated with eye and brain abnormalities.
Mazereeuw-Hautier et al.
Arch Dermatol 2006;142:994-998.
ABSTRACT
| FULL TEXT
Hereditary Vascular Anomalies: New Insights Into Their Pathogenesis
Tille and Pepper
Arterioscler. Thromb. Vasc. Bio. 2004;24:1578-1590.
ABSTRACT
| FULL TEXT
Topical Review: Pathophysiology of Sturge-Weber Syndrome
Comi
J Child Neurol 2003;18:509-516.
ABSTRACT
Recent developments in lasers and the treatment of birthmarks
Waner
Arch. Dis. Child. 2003;88:372-374.
FULL TEXT
Acquired Port-wine Stains and Antecedent Trauma: Case Report and Review of the Literature
Adams and Lucky
Arch Dermatol 2000;136:897-899.
ABSTRACT
| FULL TEXT
Immunohistochemistry of Port-wine Stains and Normal Skin With Endothelium-Specific Antibodies PAL-E, Anti--ICAM-1, Anti--ELAM-1, and Anti--Factor VIIIrAg
Neumann et al.
Arch Dermatol 1994;130:879-883.
ABSTRACT
Acquired Persistent Erythematous Patch on the Neck
Flint and Wilkin
Arch Dermatol 1994;130:512-512.
ABSTRACT
Port-wine Stains
Gaylarde et al.
Arch Dermatol 1987;123:861-862.
ABSTRACT
Acquired Port-wine Stain
Colver and Ryan
Arch Dermatol 1986;122:1415-1416.
ABSTRACT
|