睾丸腺瘤合并多角症1例

A.A. Chapanov, V. Fedorenko, V. Voytsitsky, O. A. Tkachuk, A.N. Chapanova
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引用次数: 0

摘要

本文提出一个临床病例的53岁的病人入院与怀疑睾丸肿瘤。初步诊断:先天性异常。右下睾丸腺瘤样肿瘤(右侧腹股沟隐睾)。多睾。右副睾丸腹隐睾症。右侧腹股沟间接性疝。甲胎蛋白、HCG、LDH指标正常,未见转移。行右侧管束切除术、疝切开术、局部组织重排。副睾丸被Bergholz R归类为A1型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CLINICAL CASE OF TESTICULAR ADENOMA IN A PATIENT WITH POLYORCHISM
The article presents a clinical case of a 53-year-old patient admitted to the hospital with a suspected testicular tumor. Preliminary diagnosis: congenital anomaly. Adenomatoid tumor of the undescended right testicle (inguinal cryptorchidism on the right). Polyorchism. Abdominal cryptorchidism of the accessory right testicle. Irreducible indirect inguinal hernia on the right. Alpha fetoprotein, HCG, LDH indices are normal, no metastases were found. Orchofuniculectomy on the right, herniotomy, local tissue rearrangement were performed. The accessory testis was classified as Type A1 by Bergholz R.
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