ReviewJournal of investigative medicine high impact case reports
Mature Testicular Teratoma Mimicking Hydrocele in a 3-Year-Old Boy: Case Report and Literature Review.
Review in Journal of investigative medicine high impact case reports. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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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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Authors and funding
7 authors.
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Abstract
Testicular tumors are rare in children, accounting for only 1% to 2% of pediatric solid tumors. Mature teratomas (MTs) are a benign subtype that typically occur in prepubertal boys and may occasionally mimic hydroceles. We report a case of a 3-year-old boy with left testicular swelling initially suspected to be a hydrocele. Over several months, the swelling evolved into a firm, painless mass. Ultrasound and MRI revealed a multiloculated cystic lesion with internal vascularity replacing most of the testicular parenchyma. Serum tumor markers, including alpha-fetoprotein, β-human chorionic gonadotropin, and lactate dehydrogenase, were within normal limits. The patient underwent left inguinal orchiectomy, and histopathology confirmed a MT without immature or malignant elements. Postoperative recovery was uneventful. He underwent routine follow-up every 3 months for 2 years, including physical examinations, scrotal ultrasounds, and serum tumor marker assessments. Findings from the first and second follow-ups were normal, with no evidence of recurrence to date. This case underscores the importance of early imaging and tumor marker evaluation in children presenting with persistent scrotal swelling. A systematic diagnostic approach facilitates accurate diagnosis, and orchiectomy remains the standard treatment for prepubertal MTs.
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