Ovarian Cavernous Hemangioma Presenting as an Left Adnexal Mass with Elevated Ca-125: A Case Report

Authors

  • Nilüfer Onak Kandemir Department of Pathology, Zonguldak Karaelmas University Faculty of Medicine, Zonguldak
  • Tulu Emre Ekem Department of Pathology, Zonguldak Karaelmas University Faculty of Medicine, Zonguldak
  • Aykut Barut Department of Obstetrics and Gynecology, Zonguldak Karaelmas University Faculty of Medicine, Zonguldak
  • Gamze Yurdakan Department of Pathology, Zonguldak Karaelmas University Faculty of Medicine, Zonguldak
  • Arzu Sönmez Department of Pathology, Zonguldak Karaelmas University Faculty of Medicine, Zonguldak
  • Şükrü Oğuz Özdamar Department of Pathology, Zonguldak Karaelmas University Faculty of Medicine, Zonguldak

Keywords:

Ovarian hemangioma, CA-125, Cavernous hemangioma, Ovarian neoplasm

Abstract

Hemangiomas are benign vascular tumors that are rarely found in the ovaries. Ovarian hemangiomas are usually discovered incidentally at operation or autopsy. Sometimes, they present with abdominal mass and/or pain, acute abdomen, ascites or elevated CA-125 levels, simulating ovarian neoplasm. Hemangioma should be considered in the differential diagnosis of hemorrhagic ovarian lesions grossly, and proliferations of dilated blood vessels frequently seen in the hilar region of the ovary, lymphangioma, teratoma with a prominent vascular component and angiosarcoma microscopically. The treatment of choice is oophorectomy or adnexectomy, which results in a complete cure. We report a case of very rare
tumor of the ovary with an unusual presentation; an ovarian cavernous hemangioma with elevated serum CA-125 levels and uterine leiomyoma.

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Published

2008-04-23

How to Cite

1.
Onak Kandemir N, Ekem TE, Barut A, Yurdakan G, Sönmez A, Özdamar Şükrü O. Ovarian Cavernous Hemangioma Presenting as an Left Adnexal Mass with Elevated Ca-125: A Case Report. Gynecol Obstet Reprod Med [Internet]. 2008Apr.23 [cited 2024Mar.29];14(1):63-5. Available from: https://www.gorm.com.tr/index.php/GORM/article/view/436

Issue

Section

Case Reports