Literature DB >> 29217063

Capillary Malformations (Portwine Stains) of the Head and Neck: Natural History, Investigations, Laser, and Surgical Management.

Jeong Woo Lee1, Ho Yun Chung2.   

Abstract

Capillary malformations (CMs), also known as port-wine stains, are the most common type of congenital vascular malformations. Facial CM often occurs with a quasidermatomal distribution according to the sensory trigeminal nerve distribution. With time, these lesions darken progressively, and soft tissue hypertrophy, bony hypertrophy, and/or nodule formation can develop. Multiple treatments for CM have been reported. However, the mainstay and gold standard therapy for facial or aesthetically sensitive CM is still the pulsed dye laser treatment. In patients with associated soft tissue/bony hypertrophy, surgical management is helpful in restoring the normal anatomy and in re-establishing a symmetric contour.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Capillary malformation; Laser; Natural history; Port-wine stain; Surgical treatment

Mesh:

Year:  2018        PMID: 29217063     DOI: 10.1016/j.otc.2017.09.004

Source DB:  PubMed          Journal:  Otolaryngol Clin North Am        ISSN: 0030-6665            Impact factor:   3.346


  10 in total

1.  Generalised nevus flammeus, episcleral capillary malformation and glaucoma.

Authors:  Brijesh Takkar; Harsha Saxena; Bhavana Sharma; Anubha Rathi
Journal:  BMJ Case Rep       Date:  2018-10-21

2.  Discovery and Characterization of Halogenated Xanthene Inhibitors of DUSP5 as Potential Photodynamic Therapeutics.

Authors:  Ramani Ramchandran; Daniel S Sem; Robert D Bongard; Michael Lepley; Adam Gastonguay; Raulia R Syrlybaeva; Marat R Talipov; Rachel A Jones Lipinsky; Noah R Leigh; Jaladhi Brahmbhatt; Raman Kutty; Rajendra Rathore
Journal:  J Photochem Photobiol A Chem       Date:  2019-02-10       Impact factor: 4.291

Review 3.  The Pathogenesis of Port Wine Stain and Sturge Weber Syndrome: Complex Interactions between Genetic Alterations and Aberrant MAPK and PI3K Activation.

Authors:  Vi Nguyen; Marcelo Hochman; Martin C Mihm; J Stuart Nelson; Wenbin Tan
Journal:  Int J Mol Sci       Date:  2019-05-07       Impact factor: 5.923

4.  The molecular pathophysiology of vascular anomalies: Genomic research.

Authors:  Jong Seong Kim; Su-Kyeong Hwang; Ho Yun Chung
Journal:  Arch Plast Surg       Date:  2020-05-15

5.  Surgical Management of Facial Port-Wine Stain in Sturge Weber Syndrome.

Authors:  Bar Y Ainuz; Erin Marshall; S Anthony Wolfe
Journal:  Cureus       Date:  2021-01-11

6.  The Use of Neodymium-Doped Yttrium Aluminum Garnet Laser for Treatment of Hypertrophic Port-Wine Stain.

Authors:  Brittany Miles; Andrew Armenta; James Mackey
Journal:  Case Rep Dermatol Med       Date:  2022-01-25

7.  Enhanced Activation of mTOR Signaling Pathway Was Found in the Hypertrophic and Nodular Lesions of Port Wine Stains.

Authors:  Meng-Nan Xu; Qian Wang; Min Wang; Yuan Xu; Si-Ming Yuan
Journal:  Clin Cosmet Investig Dermatol       Date:  2022-04-13

8.  Individualized Surgical Management of Refractory Port-Wine Stains in the Scalp and Face: A Single-Center Retrospective Study and a Discussion of Surgical Strategies.

Authors:  Qian Wang; Chen Yong; Min Wang; Lei Cui; Si-Ming Yuan
Journal:  Clin Cosmet Investig Dermatol       Date:  2022-08-03

9.  Treatment of facial hypertrophic capillary malformations with tumescent-assisted sclerotherapy.

Authors:  Mina Kang; Kurosh Parsi
Journal:  Australas J Dermatol       Date:  2022-04-12       Impact factor: 2.481

10.  Influence of Port-wine Stains on Quality of Life of Children and Their Parents.

Authors:  Fan Jiang; Junyi Shao; Lele Chen; Nali Yang; Jingjing Liu; Zhiming Li
Journal:  Acta Derm Venereol       Date:  2021-08-16       Impact factor: 3.875

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.