睾丸旁腺瘤样肿瘤1例临床报告

A. Negre
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引用次数: 0

摘要

目的:报告一例罕见的泌尿肿瘤病例,这给外科医生提出了一个真正的挑战,即如何进行正确的诊断和保留睾丸功能。方法:采用PubMed、Lilacs等方法进行文献修订和病例报告;一名23岁男性病人,六个月前因阴囊疼痛及右侧睾丸袋肿块而被送往UFT泌尿科就诊。结果:磁共振成像证实一结节,钆增强,在右下睾丸旁区约1.4 cm。实验室检查显示肿瘤标志物和睾酮水平正常。患者接受手术,解剖病理诊断(使用免疫组织化学标记)为附睾腺瘤样肿瘤。结论:腺瘤样肿瘤是一种罕见的起源于间皮细胞的良性肿瘤。它通常在睾丸旁,主要在附睾。手术治疗包括肿瘤切除和尽可能保留睾丸和精索通路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Paratesticular Adenomatoid Tumor: Clinical Case Report
Purpose: Report of an unusual case in URO-ONCOLOGY, which imposes on the surgeon a real challenge on how to perform the correct diagnosis and preserve the testicular function. Methods: Bibliographical revision by means of PubMed and Lilacs and case report; a 23-yearold male patient sent to the Department of Urology of UFT with the complaint of pain in the scrotal and a lump in the right testicular pouch six months ago. Result: Magnetic resonance imaging confirmed a nodular image, enhanced by gadolinium, measuring 1.4 cm in the right lower paratesticular region. Laboratory evaluation showed normal tumor markers and normal Testosterone levels. The patient underwent surgery and the anatomopathological diagnosis (with the use of immunohistochemical markers) was an adenomatoid tumor of the epididymis. Conclusion: The adenomatoid tumor is a rare benign neoplasm of mesothelial origin. It is commonly paratesticular, mainly in the epididymis. Surgical treatment consists of tumor resection and preservation of the testis and spermatic pathway whenever possible.
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