Giant ovarian fibrosarcoma: A rare case report

Sex cord-stromal tumors are very rare ovarian tumors. Primary ovarian fibrosarcomas are a very rare type of sex cord-stromal tumors. They arise from superficial or deep connective tissues of fascia, tendon, periosteum, and scar. They can grow either slowly or rapidly forming a giant abdominal mass s...

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Main Authors: Pratibha Kumari (Author), Satya Kumari (Author), Jyotsna Rani (Author), Kavya Abhilashi (Author), Kshiti Atreya (Author), Deepak Kumar (Author), Vijayanand Choudhary (Author), Sangeeta Pankaj (Author), Supriya Jaiswal (Author)
Format: Book
Published: Wolters Kluwer -Medknow Publications, 2022-02-01T00:00:00Z.
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Summary:Sex cord-stromal tumors are very rare ovarian tumors. Primary ovarian fibrosarcomas are a very rare type of sex cord-stromal tumors. They arise from superficial or deep connective tissues of fascia, tendon, periosteum, and scar. They can grow either slowly or rapidly forming a giant abdominal mass similar to epithelial tumors of the ovary. Fibrosarcomas are difficult to diagnose preoperatively. Tumor marker and radiological techniques play a trivial role in preoperative diagnosis of this rare variety of sex cord-stromal tumor. Often final diagnosis is made on histopathological and immunohistochemistry reporting. Histopathological features such as high mitotic count, nuclear atypia, and herringbone pattern arrangement of spindle cells confirm a diagnosis of malignant fibrosarcoma. Ki-67 index is considered a prognostic factor for fibromatous lesions of the ovary showing aggressive nature of tumor. We report a rare case of giant ovarian fibrosarcoma in a 40-year-old woman whose diagnosis was made histopathologically due to rarity of tumor.
Item Description:2394-9031
2582-094X
10.4103/jigims.jigims_7_22