ArticleWorld journal of surgical oncology2012
Struma ovarii with follicular thyroid-type carcinoma and neuroendocrine component: case report.
Article in World journal of surgical oncology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed, 15 citations in OpenAlex.
- Optimal Strategies for the Surgical and Long-Term Management of Malignant Struma Ovarii.Case reports in endocrinology · 2026Article
- Papillary thyroid carcinoma within struma ovarii: a case report and literature review.Journal of surgical case reports · 2025Article
- Management of malignant struma ovarii: is aggressive therapy justified? Case report and literature review.Thyroid research · 2022Article
- Papillary Thyroid Cancer in a Struma Ovarii in a 17-Year-Old Nulliparous Patient: A case Report.Diagnostics (Basel, Switzerland) · 2020Article
- An unusual presentation of a papillary thyroid carcinoma in the struma ovarii in a 10 year-old girl: A case report.International journal of surgery case reports · 2018Article
- An Unusual Case of Malignant Struma Ovarii Causing Thyrotoxicosis.European thyroid journal · 2016Article
- Successful Management and Long-term Survival of Malignant Struma Ovarii with Radioactive Iodine Therapy.Indian journal of nuclear medicine : IJNM : the official journal of the Society of Nuclear Medicine, IndiaArticle
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Authors and funding
8 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Struma ovarii (SO) is a slow-growing ovarian neoplasm with thyroid tissue as its predominant component. It is an uncommon neoplasm, usually asymptomatic with an unknown risk of malignant transformation. Due to difficulties in assessing the rare biological nature and the discrepancies in the reported cases, a consensus on the appropriate treatment has not been definitively reached. A 50-year-old female was subjected to upper gut endoscopy which showed a 30-mm mass located in the gastric antrum, suggestive of mesenchimal tumor. Incidentally, a pelvic CT scan also documented a solid mass in the right adnexa, with morphological characteristics of ovarian neoplasm. The patient underwent gastrectomy, total hysterectomy, bilateral salpingo-oophorectomy with lymph node dissection, and omentectomy. Histology documented the presence of gastric cavernous angioma, and, in the right adnexa, foci of follicular thyroid-type carcinoma arising in SO with a well-differentiated neuroendocrine component.Here we report and discuss the clinical and morphological presentation of follicular thyroid-type carcinoma arising in SO. The neoplasm was discovered incidentally and had a favorable clinical outcome at 1-year follow-up.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.