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韩国青春期前睾丸肿瘤:一位外科医生20多年的经验

Prepubertal Testicular Tumors in Korea: A Single Surgeon's Experience of More Than 20 Years.

作者信息

Baik Kyungdon, Kang Minyong, Park Kwanjin, Choi Hwang

机构信息

Department of Pediatric Urology, Seoul National University Hospital, Seoul, Korea.

出版信息

Korean J Urol. 2013 Jun;54(6):399-403. doi: 10.4111/kju.2013.54.6.399. Epub 2013 Jun 12.

Abstract

PURPOSE

To present clinical and histological features of prepubertal testicular tumors through the analysis of the long-term experiences of a single surgeon.

MATERIALS AND METHODS

The charts of 48 children treated for testicular tumors from 1986 to 2010 were retrospectively reviewed. All patients underwent radical orchiectomy. The patients' ages, clinical presentations, histopathological findings, kinetics of tumor markers, and outcomes were recorded.

RESULTS

The patients' median age at the initial diagnosis was 19.5 months (range, 3 to 84 months). All patients presented with either a palpable mass (76%) or scrotal size discrepancy (24%). Compared with a palpable mass, scrotal size discrepancy led to delay in diagnosis by 5 months. Regarding histology, yolk sac tumors and teratomas accounted for 53% and 36% of the tumors, respectively. The mean preoperative alpha-fetoprotein (AFP) level was significantly higher in patients with yolk sac tumors than in those with teratomas (4,600 ng/mL vs. 6.3 ng/mL), and only one patient with a teratoma had a preoperative AFP value higher than 20 ng/mL. Following radical orchiectomy, 72%, 8%, and 16% of patients with a yolk sac tumor showed normalization, persistent elevation, and relapse after transient lowering of AFP, respectively. Preoperative AFP was greater in patients with non-normalization than in those with normalization. Five of six patients with non-normalization showed evidence of either vascular invasion or endolymphatic tumor emboli.

CONCLUSIONS

We found a higher number of yolk sac tumors than teratomas in patients with prepubertal testicular tumors. AFP was the most useful marker in the diagnosis and follow-up of childhood yolk sac tumors. Relapsed yolk sac tumors often showed pathological evidence of aggressiveness.

摘要

目的

通过分析一位外科医生的长期经验,介绍青春期前睾丸肿瘤的临床和组织学特征。

材料与方法

回顾性分析1986年至2010年期间48例接受睾丸肿瘤治疗的儿童病历。所有患者均接受根治性睾丸切除术。记录患者的年龄、临床表现、组织病理学结果、肿瘤标志物动态变化及预后。

结果

初次诊断时患者的中位年龄为19.5个月(范围3至84个月)。所有患者均表现为可触及肿块(76%)或阴囊大小差异(24%)。与可触及肿块相比,阴囊大小差异导致诊断延迟5个月。在组织学方面,卵黄囊瘤和畸胎瘤分别占肿瘤的53%和36%。卵黄囊瘤患者术前甲胎蛋白(AFP)平均水平显著高于畸胎瘤患者(4600 ng/mL对6.3 ng/mL),只有1例畸胎瘤患者术前AFP值高于20 ng/mL。根治性睾丸切除术后,卵黄囊瘤患者中72%、8%和16%分别表现为AFP正常化、持续升高及短暂降低后复发。AFP未正常化患者的术前AFP水平高于正常化患者。6例未正常化患者中有5例显示血管侵犯或淋巴管内肿瘤栓子的证据。

结论

我们发现青春期前睾丸肿瘤患者中卵黄囊瘤的数量多于畸胎瘤。AFP是儿童卵黄囊瘤诊断和随访中最有用的标志物。复发的卵黄囊瘤常显示侵袭性的病理证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb0c/3685641/9239d4ff1beb/kju-54-399-g001.jpg

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