A rare case report: Acquired vulva lymphangioma in a young female post tubercular lymphadenitis

Marissa Astari and Afif Nurul Hidayati, NIDN8855610016 (2019) A rare case report: Acquired vulva lymphangioma in a young female post tubercular lymphadenitis. Dermatology Press, 11 (1(S)). pp. 178-179. ISSN 20367392

[img] Text (Similarity)
A Rare Case Report.pdf

Download (990kB)
[img] Text (Peer Review)
A rare case report.pdf

Download (1MB)
[img] Text (Artikel)
A Rare Case Report.pdf
Available under License Creative Commons Attribution Non-commercial.

Download (1MB)
Official URL: https://www.pagepress.org/journals/index.php/dr/ar...

Abstract

Lymphangioma are rare benign proliferations of the lymphatic system. Acquired lymphangioma circumscriptum of the vulva is a superficial lymphatic malformation, presenting as lymph-filled micro-to macro-scopic vesicles. We describe a rare case of acquired vulva lymphangioma resulting from tubercular lymphadenitis. A 20-yearold female came to Dermatology and Venereology Outpatient Clinic of Dr.Soetomo General Hospital with chief complain there were multiple clusters vesicles on her genitalia since three months ago. The vesicles followed with discomfort and slightly itchy. There was a lymphedema on both of her inguinal since 5 years ago. She was diagnosed with tubercular lymphadenitis in 13 years old of age. No history of sexual transmitted disease. She had 5 times of cryotherapy and it early got remission.

Item Type: Article
Uncontrolled Keywords: Vulva lymphangioma, Lymphangioma circumscriptum
Subjects: R Medicine > R Medicine (General)
R Medicine > RL Dermatology
Divisions: 01. Fakultas Kedokteran > Ilmu Penyakit Kulit
Creators:
CreatorsNIM/NIDN
Marissa AstariUNSPECIFIED
Afif Nurul Hidayati, NIDN8855610016afif_nurulhidayati@fk.unair.ac.id
Depositing User: hanif kurniawan
Date Deposited: 24 Sep 2019 08:08
Last Modified: 24 Sep 2019 08:08
URI: http://repository.unair.ac.id/id/eprint/87014
Sosial Share:

Actions (login required)

View Item View Item