{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,27]],"date-time":"2026-08-27T14:19:31Z","timestamp":1787840371973,"version":"build-2784847793"},"reference-count":14,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"2","license":[{"start":{"date-parts":[[2025,4,1]],"date-time":"2025-04-01T00:00:00Z","timestamp":1743465600000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-sa\/4.0"}],"content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2025,4]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>Ovarian angiosarcomas are rare tumors, with an incidence of one in 1,000,000 malignant ovarian tumors, which may present in a background of carcinosarcoma or teratoma. However, primary pure ovarian angiosarcoma is even rarer with a few cases published in the literature. Here, we present a case of a perimenopausal woman who presented with a 16 cm adnexal mass. She underwent bilateral salpingo-oophorectomy with omentectomy, which on histopathological examination revealed an ovarian angiosarcoma with tumor deposits in the pelvic peritoneum. No other component was demonstrable within the tumor, in light of which it was reported as a primary pure ovarian angiosarcoma. She received adjuvant paclitaxel- and carboplatin-based chemotherapy after discussion in a multispecialty tumor board. This case highlights the gross and microscopic findings of primary ovarian angiosarcomas and their distinction from their differential diagnosis.<\/jats:p>","DOI":"10.4103\/ijc.ijc_782_21","type":"journal-article","created":{"date-parts":[[2025,8,11]],"date-time":"2025-08-11T17:00:26Z","timestamp":1754931626000},"page":"297-300","update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":0,"title":["Primary pure angiosarcoma of the ovary: A case report"],"prefix":"10.4103","volume":"62","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-1419-2755","authenticated-orcid":false,"given":"Ankur","family":"Kumar","sequence":"first","affiliation":[{"name":"Department of Pathology, Rajiv Gandhi Cancer Institute and Research Centre, New Delhi, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-0607-4639","authenticated-orcid":false,"given":"Anila","family":"Sharma","sequence":"additional","affiliation":[{"name":"Department of Pathology, Rajiv Gandhi Cancer Institute and Research Centre, New Delhi, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-0711-1718","authenticated-orcid":false,"given":"Meenakshi","family":"Kamboj","sequence":"additional","affiliation":[{"name":"Department of Pathology, Rajiv Gandhi Cancer Institute and Research Centre, New Delhi, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-3399-0587","authenticated-orcid":false,"given":"Tanu","family":"Agrawal","sequence":"additional","affiliation":[{"name":"Department of Pathology, Shri Ram Murti Smarak Institute of Medical Sciences, Bareilly, Uttar Pradesh, India"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","published-online":{"date-parts":[[2025,8,11]]},"reference":[{"key":"R1-20250812","doi-asserted-by":"crossref","first-page":"47","DOI":"10.1186\/1752-1947-8-47","article-title":"Ovarian angiosarcoma:A case report and review of the literature","volume":"8","author":"Yaqoob","year":"2014","journal-title":"J Med Case Rep"},{"key":"R2-20250812","doi-asserted-by":"crossref","first-page":"369","DOI":"10.1002\/ssu.2980100510","article-title":"Gynecological sarcomas","volume":"10","author":"Disaia","year":"1994","journal-title":"Semin Surg Oncol"},{"key":"R3-20250812","doi-asserted-by":"crossref","first-page":"21","DOI":"10.1186\/s13048-021-00771-7","article-title":"Primary ovarian angiosarcoma:A rare and recognizable ovarian tumor","volume":"14","author":"Ye","year":"2021","journal-title":"J Ovarian 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Pathol"},{"key":"R7-20250812","doi-asserted-by":"crossref","first-page":"620","DOI":"10.1097\/00000478-199805000-00014","article-title":"Angiosarcoma of the ovary:Clinicopathologic and immunohistochemical analysis of four cases with a broad morphologic spectrum","volume":"22","author":"Nucci","year":"1998","journal-title":"Am J Surg Pathol"},{"key":"R8-20250812","doi-asserted-by":"crossref","first-page":"528","DOI":"10.1097\/COC.0b013e31827defa1","article-title":"Primary angiosarcoma of bone:A retrospective analysis of 60 patients from two institutions","volume":"37","author":"Palmerini","year":"2014","journal-title":"Am J Clin Oncol"},{"key":"R9-20250812","first-page":"295","article-title":"Metastatic angiosarcoma of the ovary","volume":"17","author":"Patel","year":"1991","journal-title":"Eur J Surg Oncol"},{"key":"R10-20250812","doi-asserted-by":"crossref","first-page":"396","DOI":"10.1111\/j.1365-2559.2005.02098.x","article-title":"Expression of D2-40 in lymphatic endothelium of 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chemotherapy","volume":"4","author":"Guseh","year":"2013","journal-title":"Gynecol Oncol Reports"},{"key":"R14-20250812","doi-asserted-by":"crossref","first-page":"1474","DOI":"10.1001\/archsurg.1991.01410360044008","article-title":"Vascular soft-tissue sarcomas:An analysis of tumor-related mortality","volume":"126","author":"Karpeh","year":"1991","journal-title":"Arch Surg"}],"container-title":["Indian Journal of 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