ArticleMedicine2017
Mucinous tumor arising in a giant sacrococcygeal teratoma: A rare case report.
Article in Medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
2 citing papers in PubMed, 4 citations in OpenAlex.
- Sacrococcygeal teratoma in an adult containing a mucinous adenocarcinoma.BMJ case reports · 2020Article
- Signet ring cell carcinoma arising from sacrococcygeal teratoma: a case report and review of the literature.The Journal of international medical research · 2019Review
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Authors and funding
4 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
rationaleTeratomas, which most frequently affect adult females, are the most common type of germ cell tumor, it always comprises derivatives of at least 2 germ layers. The most common site of primary teratomas is the ovary. Sacrococcygeal teratomas (SCTs), which are exceedingly rare in adults, are generally found in newborns or children. PATIENT CONCERNS: A 39-year-old woman presented to our clinic with a 1-year history of gradually aggravated difficulty in micturition and defecation, and a tumor in her right buttock present since birth. Appropriate preoperative examinations showed a large (15.6 cm × 12.2 cm × 30.0 cm) multicystic SCT. DIAGNOSES: Histologic examination confirmed a mucinous tumor arising in a giant SCT.
interventionsAbdominoperineal rectal resection was performed. OUTCOMES: The patient recovered well and was discharged on day 33 of admission. LESSONS: We report the first case of a mucinous tumor arising in an SCT, in which the teratoma presented mature tissue elements derived only from the endodermal germ layer (keratinous debris).
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