Giant bilateral prepubertal-type teratomas in a postpubertal patient: An illustrative case and review of the literature.

IF 3.4 3区 医学 Q1 PATHOLOGY Virchows Archiv Pub Date : 2024-07-01 Epub Date: 2024-01-02 DOI:10.1007/s00428-023-03723-2
Katrina Collins, William J Anderson, Michelle S Hirsch, Thomas M Ulbright, Andres M Acosta
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Abstract

Prepubertal-type teratomas are uncommon, especially in postpubertal male patients. We document a case of a 28-year-old man with a lifelong history of bilateral testicular masses who presented with scrotal fistulas and no clinical evidence of extratesticular disease. Bilateral radical orchiectomies demonstrated large bilateral solid and cystic masses that contained grossly visible hairs. Microscopically, both tumors consisted of pure teratomas comprising a mixture of mature tissues derived from the three embryonic layers. Germ cell neoplasia in situ was not identified, and fluorescence in situ hybridization studies demonstrated the absence of i(12p), supporting a diagnosis of prepubertal-type teratoma. The absence of metastases in this patient with longstanding tumors highlights the benign nature of prepubertal-type teratomas affecting postpubertal patients. Furthermore, this case illustrates that at least a subset of prepubertal-type teratomas seen in adult men represent a late diagnosis of a largely pediatric entity. Additionally, we performed a comprehensive review of the literature on this topic.

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一名青春期后患者的双侧巨大青春期前型畸胎瘤:一个典型病例和文献综述。
青春期前型畸胎瘤并不常见,尤其是在青春期后的男性患者中。我们记录了一例 28 岁的男性病例,他终身患有双侧睾丸肿块,并伴有阴囊瘘,但没有睾丸外疾病的临床证据。双侧根治性睾丸切除术显示出双侧巨大的实性和囊性肿块,肿块中含有粗略可见的毛发。显微镜下,两个肿瘤均为纯畸胎瘤,由来自三个胚层的成熟组织混合而成。未发现生殖细胞原位瘤,荧光原位杂交研究显示没有i(12p),支持青春期前型畸胎瘤的诊断。这名肿瘤长期存在的患者没有发生转移,这凸显了影响青春期后患者的青春期前型畸胎瘤的良性性质。此外,该病例还说明,至少有一部分在成年男性中出现的青春期前型畸胎瘤是一种晚期诊断的畸胎瘤。此外,我们还对有关这一主题的文献进行了全面回顾。
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来源期刊
Virchows Archiv
Virchows Archiv 医学-病理学
CiteScore
7.40
自引率
2.90%
发文量
204
审稿时长
4-8 weeks
期刊介绍: Manuscripts of original studies reinforcing the evidence base of modern diagnostic pathology, using immunocytochemical, molecular and ultrastructural techniques, will be welcomed. In addition, papers on critical evaluation of diagnostic criteria but also broadsheets and guidelines with a solid evidence base will be considered. Consideration will also be given to reports of work in other fields relevant to the understanding of human pathology as well as manuscripts on the application of new methods and techniques in pathology. Submission of purely experimental articles is discouraged but manuscripts on experimental work applicable to diagnostic pathology are welcomed. Biomarker studies are welcomed but need to abide by strict rules (e.g. REMARK) of adequate sample size and relevant marker choice. Single marker studies on limited patient series without validated application will as a rule not be considered. Case reports will only be considered when they provide substantial new information with an impact on understanding disease or diagnostic practice.
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