[睾丸表皮样囊肿：一种罕见病症]
[Testicular epidermoid cyst: A rare entity].
作者信息
Sáez Barranquero Felipe, Regaña Feijoo MarÍa José, Del Río González Sergio, García Del Pino MarÍa José, Cantero Mellado Juan Andrés, Herrera Imbroda Bernardo, Marchal Escalona Cristobal, Machuca Santa Cruz Francisco Javier
机构信息
Department of Unit of Clinical Management I Intercentre of Urology. Hospital Ronda. Málaga. Spain.
Department of Radiology. Hospital Virgen de la Victoria. Málaga. Spain.
出版信息
Arch Esp Urol. 2015 Oct;68(8):672-5.
OBJECTIVE
Testicular epidermoid cyst is a rare clinical entity that accounts for 1% of testicular neoplasias.
METHODS AND RESULTS
We report two cases of testicular epidermoid cysts in a 18 and 19 year old males with a painless testicular lesion. Testicular US was carried out showing a hypoechoic nodule in both cases. With the suspicion of testicular neoplasm inguinal orchiectomy was carried out with placement of testicular prostheses in the same act. The pathology report was testicular epidermoid cyst in both cases.
CONCLUSIONS
Testicular epidermoid cysts are an uncommon benign entity. When there is a suspicion of this diagnosis, based on tumor markers and ultrasound or MRI images, testicular parenchyma-sparing surgery must be attempted.
目的
睾丸表皮样囊肿是一种罕见的临床病症，占睾丸肿瘤的1%。
方法与结果
我们报告两例睾丸表皮样囊肿病例，患者为18岁和19岁男性，均有无痛性睾丸病变。两例患者均进行了睾丸超声检查，显示为低回声结节。由于怀疑睾丸肿瘤，遂行腹股沟睾丸切除术，并同期植入睾丸假体。两例病例的病理报告均为睾丸表皮样囊肿。
结论
睾丸表皮样囊肿是一种不常见的良性病症。当基于肿瘤标志物以及超声或磁共振成像怀疑为此诊断时，必须尝试保留睾丸实质的手术。
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