Adult intratesticular splenogonadal fusion simulating testicular cancer: a diagnostic blind spot in modern urologic oncology.

IF 0.5 Q4 SURGERY
Journal of Surgical Case Reports Pub Date : 2026-09-29 eCollection Date: 2026-09-01 DOI:10.1093/jscr/rjag863
Grace El Nabbout, John J Kowalczyk, Kelly J Manahan
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引用次数: 0

Abstract

Splenogonadal fusion (SGF) remains one of the rarest and most diagnostically deceptive causes of scrotal pathology, frequently mimicking the clinical and imaging features of testicular malignancy despite its benign histology. Its exceptional rarity in adults, combined with the absence of reliable noninvasive preoperative diagnostic criteria, creates a major challenge in urologic practice, often necessitating management driven by concern for cancer. We present a 29-year-old man with a symptomatic left testicular mass and imaging highly suspicious for malignancy, prompting radical inguinal orchiectomy after standard evaluation could not confidently exclude a testicular neoplasm. Unexpectedly, final histopathology demonstrated ectopic splenic tissue consistent with SGF without evidence of germ cell tumour or other malignancy. This case highlights the persistent gap between preoperative suspicion and definitive diagnosis, emphasizing the importance of recognizing rare benign entities that closely imitate testicular cancer and may still lead to radical surgery in otherwise healthy young adults unnecessarily.

成人睾丸内脾性腺融合模拟睾丸癌:现代泌尿肿瘤学的诊断盲点。
脾性腺融合(SGF)仍然是阴囊病理最罕见和诊断上最具欺骗性的原因之一,尽管其组织学为良性,但经常模仿睾丸恶性肿瘤的临床和影像学特征。它在成人中罕见,再加上缺乏可靠的无创术前诊断标准,这给泌尿外科实践带来了重大挑战,往往需要由癌症驱动的管理。我们报告一名29岁男性,有症状的左侧睾丸肿块,影像学高度怀疑为恶性肿瘤,在标准评估后不能肯定地排除睾丸肿瘤,促使腹股沟根治性睾丸切除术。出乎意料的是,最终的组织病理学显示异位脾组织与SGF一致,没有生殖细胞肿瘤或其他恶性肿瘤的证据。本病例强调了术前怀疑与最终诊断之间的持续差距,强调了识别罕见良性实体的重要性,这些实体与睾丸癌非常相似,但仍可能导致健康年轻人不必要的根治性手术。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.70
自引率
0.00%
发文量
559
审稿时长
11 weeks
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