睾丸混合性畸胎瘤和卵黄囊肿瘤,青春期前型:一例病例报告及既往发表病例总结。

IF 0.7 4区 医学 Q4 PATHOLOGY Fetal and Pediatric Pathology Pub Date : 2024-03-01 Epub Date: 2023-11-09 DOI:10.1080/15513815.2023.2279132
Md Mohin, Soumya Dey, Raktim Ray, Firdous Wasim Sk, Oindrila Das, Uttara Chatterjee
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引用次数: 0

摘要

背景:睾丸混合生殖细胞瘤在青春期后很常见,在青春期前则较少。青春期前混合性畸胎瘤和卵黄囊瘤的报告仅有3例。其中两例为未成熟畸胎瘤成分,属于新生儿年龄组。第三个病例是一个蹒跚学步的孩子,有成熟的畸胎瘤成分。病例报告:一名18个月大的男孩出现睾丸肿块。血清AFP升高(2200 ng/ml)。睾丸切除标本中有一个卵黄囊肿瘤和一个小的表皮样囊肿,表明有成熟的畸胎瘤成分。结论:我们报告了一个睾丸混合畸胎瘤和卵黄囊肿瘤,青春期前型,并总结了以前发表的病例。只有一份报告描述了这种青春期前睾丸成熟畸胎瘤和卵黄囊瘤的合并。
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Testicular Mixed Teratoma and Yolk Sac Tumor, Prepubertal Type: A Case Report with Summary of Prior Published Cases.

Background: Testicular mixed germ cell tumor is common in the post-pubertal age, less so in prepuberty. There are only 3 reports of prepubertal mixed teratoma and yolk sac tumor. Two of these cases had immature teratoma component and were in the neonatal age group. The third case in a toddler had a mature teratoma component.

Case report: An 18-month-old boy presented with a testicular mass. Serum AFP was elevated (2200 ng/ml). The orchidectomy specimen contained a yolk-sac tumor and a small epidermoid cyst, indicating a mature teratomatous component.

Conclusion: We report a testicular mixed teratoma and yolk sac tumor, prepubertal type along with summary of prior published cases. There is only one report describing this combination of mature teratoma with yolk sac tumor in the prepubertal testis.

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来源期刊
CiteScore
3.00
自引率
0.00%
发文量
68
审稿时长
6-12 weeks
期刊介绍: Fetal and Pediatric Pathology is an established bimonthly international journal that publishes data on diseases of the developing embryo, newborns, children, and adolescents. The journal publishes original and review articles and reportable case reports. The expanded scope of the journal encompasses molecular basis of genetic disorders; molecular basis of diseases that lead to implantation failures; molecular basis of abnormal placentation; placentology and molecular basis of habitual abortion; intrauterine development and molecular basis of embryonic death; pathogenisis and etiologic factors involved in sudden infant death syndrome; the underlying molecular basis, and pathogenesis of diseases that lead to morbidity and mortality in newborns; prenatal, perinatal, and pediatric diseases and molecular basis of diseases of childhood including solid tumors and tumors of the hematopoietic system; and experimental and molecular pathology.
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