Malignant Brenner tumor of the ovary: Review and case report

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Malignant Brenner tumor of the ovary: Review and case report

Ovarian neoplasms are a heterogeneous group of tumors with varying incidence in the general population. The most common are the surface epithelial tumors which include transitional cell tumors. Transitional cell tumors include both transitional cell carcinoma and Brenner tumor. The vast majority of Brenner tumors are benign, often incidental findings; however, malignant Brenner tumors (MBT) do ...

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Malignant brenner tumor of ovary.

Brenner tumor is a relatively uncommon neoplasm. It constitutes 1.4–2.5 % of all ovarian tumors and has a predilection for the postmenopausal women. Most Brenner tumors are benign, with only 2–5 % being malignant. The malignant components of the tumor, which show heterogeneous epithelial growth and atypia with intervening stroma, consist of transitional cells, squamous or undifferentiated carci...

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MALIGNANT HISTIOCYTOSIS: A CASE REPORT AND REVIEW OF THE LITERATURE

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[Brenner tumor: one case report and bibliographic review].

Brenner tumor is a rare tumor that represents approximately 1.5% of the tumors of ovary. It is defined as a tumor of transitional cells composed by urothelial cells arranged in solid or cystic groups absorbed in a fibrous stroma. It classifies in benign Brenner tumor (95%), borderline (3-4%) and malignant (1%). Let's sense beforehand the clinical case of a 46-year-old patient who underwent surg...

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Glomus Tumor of Uncertain Malignant Potential in Thumb: A Case Report and Review of Literature

Malignant transformation of glomus tumor is exceedingly rare and most common reported in lower extremity and abdominal viscera. We could find only 6 previous case report of malignant glomus tumor in the hand. Although large and deeply located glomus tumors are considered to be malignant, evidence has shown that most of these cases were clinically benign. These lesions are better considered as g...

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ژورنال

عنوان ژورنال: Gynecologic Oncology Reports

سال: 2017

ISSN: 2352-5789

DOI: 10.1016/j.gore.2017.07.001