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青春期前儿童不可触及性睾丸间质细胞瘤的保留睾丸手术

Testis-Sparing Surgery for Non-Palpable Leydig Cell Tumors in Prepubertal Children.

作者信息

Lambropoulos Vassilis, Theodorakopoulos Antonios, Mouravas Vasileios, Pazarli Elissavet, Godosis Dimitrios, Kepertis Chrysostomos, Anastasiadis Kleanthis, Spyridakis Ioannis

机构信息

2nd Paediatric Surgery Department, Aristotle University of Thessaloniki, "Papageorgiou" General Hospital, 56403 Thessaloniki, Greece.

Radiology Department, "Papageorgiou" General Hospital, 56403 Thessaloniki, Greece.

出版信息

Pediatr Rep. 2020 Oct 26;12(3):86-92. doi: 10.3390/pediatric12030020.

Abstract

Leydig cell tumor (LCT) is an infrequent stromal neoplasm of the testis with an incidence of less than 3% of all gonadal tumors in the general male population. Only 25% is found in prepubertal children, where Leydig cell tumors are always reported benign. The hospital records of two prepubertal male children, who underwent organ sparing surgery for testicular LCT the last five years, were retrospectively reviewed. In both of them, the lesion was incidentally found during a scrotal ultrasonography for testicular pain. The diagnosis of a benign LCT was based on the pre-operative physical examination and imaging (Ultrasound-US, Magnetic Resonance Imaging-MRI) as well as the negative tumor markers. A testicle-sparing procedure was decided and the pathologic examination of the surgical specimen confirmed the diagnosis. No tumor recurrence was noted on follow-up. Testis-sparing surgery provides the possibility of complete excision of such lesions and should be considered as the treatment of choice.

摘要

睾丸间质细胞瘤(LCT)是一种罕见的睾丸间质肿瘤,在一般男性人群中,其发病率不到所有性腺肿瘤的3%。仅25%见于青春期前儿童,在该群体中,睾丸间质细胞瘤均被报告为良性。回顾性分析了过去五年中因睾丸LCT接受保留器官手术的两名青春期前男性儿童的医院记录。在他们两人中,病变均在因睾丸疼痛进行阴囊超声检查时偶然发现。良性LCT的诊断基于术前体格检查、影像学检查(超声-US、磁共振成像-MRI)以及肿瘤标志物阴性。决定实施保留睾丸手术,手术标本的病理检查证实了诊断。随访期间未发现肿瘤复发。保留睾丸手术提供了完全切除此类病变的可能性,应被视为首选治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b93/7717655/b7a6949d21d3/pediatrrep-12-00020-g001.jpg

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