ArticleCureus2024
An Atypical Presentation of a Pediatric Mature Teratoma: A Case Report and Review of the Literature.
Article in Cureus, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
What it found
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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.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
3 citing papers in PubMed.
- Mature Cystic Teratoma of the Right Adrenal Gland in a Pediatric Patient: A Case Report.Clinical case reports · 2026Article
- Article
- Mature Testicular Teratoma Mimicking Hydrocele in a 3-Year-Old Boy: Case Report and Literature Review.Journal of investigative medicine high impact case reportsReview
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Immature teratoma is an uncommon type of malignant tumor that mostly consists of immature tissue originating from the neuroepithelium. Mature teratomas in pediatrics are relatively rare and difficult to diagnose because of various symptoms and the tendency to overlap with other illnesses. This study aimed to report a rare case of a mature teratoma in pediatric age. A Saudi female patient, aged 31 months, was brought to the emergency room (ER) in 2024 with a suprapubic mass. She did not complain of pain or urinary symptoms and had no substantial medical or family history, and the mass was discovered incidentally. A non-tender suprapubic mass was found during a physical examination. A large cystic mass containing fat and calcification was seen during imaging tests (pelvic CT and MRI), and this diagnosis was consistent with the presence of an ovarian dermoid cyst. The surgical intervention involved laparotomy with right oophorectomy, and the tumor was identified by pathological investigation as a mature teratoma, distinguished by a cystic structure packed with hair, gelatinous material, and bone components. Following the surgery, there were no issues, and a follow-up appointment was scheduled to monitor any complications. This case emphasizes the rarity and difficulties in diagnosing mature teratomas in pediatric patients, with positive and promising outcomes highlighting that a comprehensive diagnostic approach and a customized treatment plan are essential for a smooth recovery from ovarian lesions in pediatrics. Consequently, accurate diagnosis and quick surgical intervention are critical for optimal management, even in the absence of obvious symptoms.
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Registered trials
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