Retroperitoneal Cellular Angiofibroma: A Rare Gynecological Entity

Detalhes bibliográficos
Autor(a) principal: Brandão, Ana
Data de Publicação: 2017
Outros Autores: Campos, Sara, Fraga, João, Silva, Teresa, Águas, Fernanda
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/8774
Resumo: Cellular angiofibroma is a mesenchymal tumor, described in 1997, without gender preference, that usually appears at age 40. The vulvovaginal area is the most common site in women, mimicking vulvar benign tumors, like Bartholin gland cyst. However, there are a few described cases of a deep or extra-pelvic angiofibroma. Excision is the treatment of choice and the recurrence rate appears to be low. We present the case of a woman with a heterogeneous tumor in the right adnexial region. At the surgery, a retroperitoneal tumor was excised and the histopathological tissue analysis revealed a cellular angiofibroma.
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spelling Retroperitoneal Cellular Angiofibroma: A Rare Gynecological EntityAngiofibroma Celular Retroperitoneal: Uma Entidade Rara na GinecologiaAngiofibromaRetroperitoneal NeoplasmsAngiofibromaNeoplasias RetroperitoneaisCellular angiofibroma is a mesenchymal tumor, described in 1997, without gender preference, that usually appears at age 40. The vulvovaginal area is the most common site in women, mimicking vulvar benign tumors, like Bartholin gland cyst. However, there are a few described cases of a deep or extra-pelvic angiofibroma. Excision is the treatment of choice and the recurrence rate appears to be low. We present the case of a woman with a heterogeneous tumor in the right adnexial region. At the surgery, a retroperitoneal tumor was excised and the histopathological tissue analysis revealed a cellular angiofibroma.O angiofibroma celular é uma entidade tumoral mesenquimatosa rara, descrita pela primeira vez em 1997, sem predomínio de género e que surge tendencialmente na quarta década de vida. A localização mais habitual na mulher é superficial a nível da região vulvovaginal, confundindo-se muitas vezes a nível vulvar com quisto/tumor da glândula de Bartholin. No entanto, estão descritos alguns casos de tumor em localização profunda e extra-pélvica. O tratamento é excisional e a recorrência é baixa. É apresentado um caso de uma paciente com uma formação heterogénea a nível da região anexial direita, cuja cirurgia mostrou tratar-se de uma formação nodular alongada, retroperitoneal, localizada a nível dos espaços paracervical e paravesical direitos, que se excisou. O estudo histológico revelou tumor mesenquimatoso compatível com angiofibroma celular. Ordem dos Médicos2017-12-29info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfapplication/vnd.openxmlformats-officedocument.wordprocessingml.documentapplication/vnd.openxmlformats-officedocument.wordprocessingml.documentapplication/vnd.openxmlformats-officedocument.wordprocessingml.documentapplication/vnd.openxmlformats-officedocument.wordprocessingml.documentapplication/vnd.openxmlformats-officedocument.wordprocessingml.documentapplication/pdfapplication/vnd.openxmlformats-officedocument.wordprocessingml.documentimage/jpegapplication/pdfhttps://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/8774oai:ojs.www.actamedicaportuguesa.com:article/8774Acta Médica Portuguesa; Vol. 30 No. 12 (2017): December; 882-886Acta Médica Portuguesa; Vol. 30 N.º 12 (2017): Dezembro; 882-8861646-07580870-399Xreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAPporhttps://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/8774https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/8774/5276https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/8774/9085https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/8774/9086https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/8774/9087https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/8774/9088https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/8774/9089https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/8774/9125https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/8774/9326https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/8774/9483https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/8774/9828Direitos de Autor (c) 2017 Acta Médica Portuguesainfo:eu-repo/semantics/openAccessBrandão, AnaCampos, SaraFraga, JoãoSilva, TeresaÁguas, Fernanda2022-12-20T11:05:37Zoai:ojs.www.actamedicaportuguesa.com:article/8774Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T16:19:38.397146Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Retroperitoneal Cellular Angiofibroma: A Rare Gynecological Entity
Angiofibroma Celular Retroperitoneal: Uma Entidade Rara na Ginecologia
title Retroperitoneal Cellular Angiofibroma: A Rare Gynecological Entity
spellingShingle Retroperitoneal Cellular Angiofibroma: A Rare Gynecological Entity
Brandão, Ana
Angiofibroma
Retroperitoneal Neoplasms
Angiofibroma
Neoplasias Retroperitoneais
title_short Retroperitoneal Cellular Angiofibroma: A Rare Gynecological Entity
title_full Retroperitoneal Cellular Angiofibroma: A Rare Gynecological Entity
title_fullStr Retroperitoneal Cellular Angiofibroma: A Rare Gynecological Entity
title_full_unstemmed Retroperitoneal Cellular Angiofibroma: A Rare Gynecological Entity
title_sort Retroperitoneal Cellular Angiofibroma: A Rare Gynecological Entity
author Brandão, Ana
author_facet Brandão, Ana
Campos, Sara
Fraga, João
Silva, Teresa
Águas, Fernanda
author_role author
author2 Campos, Sara
Fraga, João
Silva, Teresa
Águas, Fernanda
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Brandão, Ana
Campos, Sara
Fraga, João
Silva, Teresa
Águas, Fernanda
dc.subject.por.fl_str_mv Angiofibroma
Retroperitoneal Neoplasms
Angiofibroma
Neoplasias Retroperitoneais
topic Angiofibroma
Retroperitoneal Neoplasms
Angiofibroma
Neoplasias Retroperitoneais
description Cellular angiofibroma is a mesenchymal tumor, described in 1997, without gender preference, that usually appears at age 40. The vulvovaginal area is the most common site in women, mimicking vulvar benign tumors, like Bartholin gland cyst. However, there are a few described cases of a deep or extra-pelvic angiofibroma. Excision is the treatment of choice and the recurrence rate appears to be low. We present the case of a woman with a heterogeneous tumor in the right adnexial region. At the surgery, a retroperitoneal tumor was excised and the histopathological tissue analysis revealed a cellular angiofibroma.
publishDate 2017
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dc.publisher.none.fl_str_mv Ordem dos Médicos
publisher.none.fl_str_mv Ordem dos Médicos
dc.source.none.fl_str_mv Acta Médica Portuguesa; Vol. 30 No. 12 (2017): December; 882-886
Acta Médica Portuguesa; Vol. 30 N.º 12 (2017): Dezembro; 882-886
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