A Case of Vulvar Lymphangiectasia secondary to Primary Lymphedema.
- Author:
Jung Min CHOI
1
;
Chul Jong PARK
;
Jong Yook YI
Author Information
1. Department of Dermatology, College of Medicine, The Catholic University of Korea, Seoul, Korea.
- Publication Type:Case Report
- Keywords:
Lymphangiectasia;
Primary lymphedema
- MeSH:
Adolescent;
Cicatrix;
Female;
Humans;
Inflammation;
Leg;
Lymphangioma;
Lymphedema*;
Rare Diseases
- From:Korean Journal of Dermatology
2000;38(6):818-820
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Lymphangiectasia (acquired lymphangioma) is a rare disease that resembles congenital lymphangioma clinically and histopathologically. It usually occurs as a result of acquired lymphatic obstruction secondary to surgery, irradiation, recurrent infection, primary or secondary lymphedema, pressure, and scar due to chronic inflammation, etc. We herein report a case of vulvar lymphangiectasia of a 15-year-old female. She has suffered from swelling on both legs since the age of 5. She was presented because of multiple grouped vesicles and papules containing clear fluid, which resembled frog's spawn and has developed on the vulvar area since the age of 9.
