ReviewThe Journal of international medical research2019
Signet ring cell carcinoma arising from sacrococcygeal teratoma: a case report and review of the literature.
Review in The Journal of international medical research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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3 citing papers in PubMed, 7 citations in OpenAlex.
- Sacrococcygeal teratoma in a 10-year-old-female: a rare case report from Nepal.Annals of medicine and surgery (2012) · 2025Article
- Adenocarcinoma With Intestinal and Pancreatobiliary Features Arising From a Sacrococcygeal Teratoma in an Adult Female: A Case Report.Case reports in pathology · 2025Article
- Sacrococcygeal teratoma in an adult female patient-case report and review of literature.Journal of surgical case reports · 2024Article
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Authors and funding
6 authors at 1 institution in 1 country.
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No grant is acknowledged in the PubMed record.
Abstract
We report here a rare case of adult sacrococcygeal teratoma (SCT) that was pathologically diagnosed as signet ring cell carcinoma (SRCC). A 26-year-old man complained of lower abdominal distension and discomfort and difficulty in urinating, and he was admitted to our hospital. Pelvic magnetic resonance imaging showed multiple oval, solid-cystic masses around the anterior sacrococcygeal region that measured approximately 96 × 114 × 89 mm. Magnetic resonance imaging also showed irregular cysts around the posterior sacrococcygeal region that measured approximately 34 × 72 × 60 mm. The preliminary diagnosis was cystic SCT. The patient then underwent surgery, during which we incised the cysts. A large amount of viscous, jelly-like liquid was present in the anterior sacrococcygeal mass. Furthermore, a large amount of light yellow, porridge-like secretion was present in the posterior sacrococcygeal mass. A pathological examination and immunohistochemistry confirmed teratoma, specifically SRCC.
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