Department of Day Surgery, National Clinical Research Center for Child Health and Disorders, Ministry of Education, Key Laboratory of Child Development and Disorder, Children's Hospital of Chongqing Medical University, Chongqing, China.
China International Science and Technology Cooperation Base of Child Development and Critical Disorders, Chongqing, China.
Pediatr Surg Int. 2024 Jul 2;40(1):165. doi: 10.1007/s00383-024-05750-9.
This study aims to examine the clinical characteristics and surgical management of pediatric testicular epidermoid cysts, thereby contributing to the existing body of knowledge pertinent to the diagnosis and therapeutic intervention s for this condition.
A retrospective analysis was conducted on the clinical records of 23 pediatric patients diagnosed with testicular epidermoid cysts, who were admitted to our institution between April 2013 and February 2024. Concurrently, a comprehensive review and analysis of pertinent literature were undertaken to augment the findings.
The mean age at which the onset of epidermoid cysts was observed was 6.0 years. All cases were singular and unilateral. B-ultrasound diagnosis categorized 6 cases as epidermoid cysts, 11 as teratomas, and 6 as indeterminate, yielding a diagnostic sensitivity of 26.1%. All patients underwent testicle-sparing mass resection, and nine patients underwent rapid intraoperative frozen section analysis, revealing eight cases of testicular epidermoid cysts and one teratoma, with a diagnostic sensitivity of 88.89%. Postoperative histopathological examination confirmed the diagnosis of testicular epidermoid cyst.
Pediatric testicular epidermoid cysts are an uncommon occurrence, primarily presenting as a painless scrotal mass, which can mimic the clinical features of malignant testicular tumors. Imaging modalities and histopathological assessment are pivotal in the diagnostic process for pediatric testicular epidermoid cysts. For cases where B-ultrasound is inconclusive, rapid intraoperative pathological examination should be considered.
本研究旨在探讨小儿睾丸表皮样囊肿的临床特征和手术治疗方法,以期为该疾病的诊断和治疗提供参考。
对 2013 年 4 月至 2024 年 2 月期间在我院就诊的 23 例小儿睾丸表皮样囊肿患者的临床资料进行回顾性分析,并对相关文献进行综合复习和分析。
表皮样囊肿的平均发病年龄为 6.0 岁,均为单发单侧病变。B 超诊断 6 例为表皮样囊肿,11 例为畸胎瘤,6 例为不确定,诊断灵敏度为 26.1%。所有患者均行保留睾丸的肿块切除术,9 例行快速术中冰冻切片分析,结果显示 8 例为睾丸表皮样囊肿,1 例为畸胎瘤,诊断灵敏度为 88.89%。术后组织病理学检查证实为睾丸表皮样囊肿。
小儿睾丸表皮样囊肿较为少见,主要表现为无痛性阴囊肿块,其临床表现可类似于恶性睾丸肿瘤。影像学检查和组织病理学评估是小儿睾丸表皮样囊肿诊断的关键。对于 B 超检查结果不明确的病例,应考虑行快速术中病理检查。