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Ovarian Hemangioma: a Rare Case Report and Review of the Literature

Ovarian hemangiomas are benign and rare tumors of female genital tract with less than 60 reported cases in the literature. A 38- yr- old woman was admitted to Be’sat Hospital, Tehran, Iran in 2012, due to severe abdominal pain. Ultrasound evaluation revealed a 6 cm left ovarian cystic mass and serum...

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Detalles Bibliográficos
Autores principales: Ziari, Katayoun, Alizadeh, Kamyab
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Iranian Society of Pathology 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4749197/
https://www.ncbi.nlm.nih.gov/pubmed/26870145
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author Ziari, Katayoun
Alizadeh, Kamyab
author_facet Ziari, Katayoun
Alizadeh, Kamyab
author_sort Ziari, Katayoun
collection PubMed
description Ovarian hemangiomas are benign and rare tumors of female genital tract with less than 60 reported cases in the literature. A 38- yr- old woman was admitted to Be’sat Hospital, Tehran, Iran in 2012, due to severe abdominal pain. Ultrasound evaluation revealed a 6 cm left ovarian cystic mass and serum tumor markers were normal. Then, left salpingo-oophorectomy was performed for the patient. Microscopic examination revealed a follicular cyst and an incidental cavernous hemangioma consisting thin-walled vascular channels filled with blood that lined with flatten endothelial cells. In IHC staining strong immunoreactivity for CD31 and CD34 were seen, finally, the diagnosis of primary ovarian hemangioma, cavernous-type was made. The clinicopathologic presentation of this unusual benign tumor is discussed.
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spelling pubmed-47491972016-02-11 Ovarian Hemangioma: a Rare Case Report and Review of the Literature Ziari, Katayoun Alizadeh, Kamyab Iran J Pathol Case Report Ovarian hemangiomas are benign and rare tumors of female genital tract with less than 60 reported cases in the literature. A 38- yr- old woman was admitted to Be’sat Hospital, Tehran, Iran in 2012, due to severe abdominal pain. Ultrasound evaluation revealed a 6 cm left ovarian cystic mass and serum tumor markers were normal. Then, left salpingo-oophorectomy was performed for the patient. Microscopic examination revealed a follicular cyst and an incidental cavernous hemangioma consisting thin-walled vascular channels filled with blood that lined with flatten endothelial cells. In IHC staining strong immunoreactivity for CD31 and CD34 were seen, finally, the diagnosis of primary ovarian hemangioma, cavernous-type was made. The clinicopathologic presentation of this unusual benign tumor is discussed. Iranian Society of Pathology 2016 /pmc/articles/PMC4749197/ /pubmed/26870145 Text en © 2016, IRANIAN JOURNAL OF PATHOLOGY This is an open-access article distributed under the terms of the Creative Commons Attribution-noncommercial 4.0 International License, (https://creativecommons.org/licenses/by-nc/4.0/) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.
spellingShingle Case Report
Ziari, Katayoun
Alizadeh, Kamyab
Ovarian Hemangioma: a Rare Case Report and Review of the Literature
title Ovarian Hemangioma: a Rare Case Report and Review of the Literature
title_full Ovarian Hemangioma: a Rare Case Report and Review of the Literature
title_fullStr Ovarian Hemangioma: a Rare Case Report and Review of the Literature
title_full_unstemmed Ovarian Hemangioma: a Rare Case Report and Review of the Literature
title_short Ovarian Hemangioma: a Rare Case Report and Review of the Literature
title_sort ovarian hemangioma: a rare case report and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4749197/
https://www.ncbi.nlm.nih.gov/pubmed/26870145
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