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A case of aggressive angiomyxoma of the vulva / 대한산부인과학회지
Article em Ko | WPRIM | ID: wpr-161758
Biblioteca responsável: WPRO
ABSTRACT
Aggressive angiomyxoma is an uncommon soft-tissue neoplasm which affects the pelvis and genital organs of the young female predominantly. This tumor has a high tendency of local recurrence, but it usually does not develop metastasis. Although surgical excision with wide tumor-free margins may be necessary to obtain a complete cure, some of patients experience local recurrences. Many of the tumors are estrogen receptor (ER) and progesterone receptor (PR) positive and medical therapy with gonadotropin-releasing hormone (GnRH) agonists showed to be effective in a few cases. We present a case of 29-years-old women who has aggressive angiomyxoma which was misdiagnosed as bartholin duct cyst. She was treated by wide local excision with postoperative adjuvant GnRH agonist therapy for 3 months. She is now free of disease during 9 months of follow up. We have described this case with the brief of literature.
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Texto completo: 1 Base de dados: WPRIM Assunto principal: Pelve / Recidiva / Vulva / Receptores de Progesterona / Seguimentos / Hormônio Liberador de Gonadotropina / Estrogênios / Genitália / Mixoma / Metástase Neoplásica Tipo de estudo: Observational_studies / Prognostic_studies Limite: Female / Humans Idioma: Ko Revista: Korean Journal of Obstetrics and Gynecology Ano de publicação: 2008 Tipo de documento: Article
Texto completo: 1 Base de dados: WPRIM Assunto principal: Pelve / Recidiva / Vulva / Receptores de Progesterona / Seguimentos / Hormônio Liberador de Gonadotropina / Estrogênios / Genitália / Mixoma / Metástase Neoplásica Tipo de estudo: Observational_studies / Prognostic_studies Limite: Female / Humans Idioma: Ko Revista: Korean Journal of Obstetrics and Gynecology Ano de publicação: 2008 Tipo de documento: Article