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原发性附睪神经母细胞瘤:一个重要的鉴别诊断。

Primary paratesticular neuroblastoma: an important differential diagnosis.

机构信息

Department of Pediatric Surgery, Virgen del Rocío Children's Hospital, Seville, Spain.

出版信息

J Pediatr Urol. 2013 Apr;9(2):e117-22. doi: 10.1016/j.jpurol.2012.10.014. Epub 2012 Nov 9.

Abstract

Primary neuroblastoma as a paratesticular tumor is extremely rare with only 8 described cases worldwide. In this article, we present the case of a 5-month-old boy with this rare tumor location and give an update on the current literature. As in our case, typically these tumors present as Stage 1 disease and simple tumorectomy alone leads to excellent outcome and long-term survival. However, unawareness of this differential diagnosis and misinterpretation of intraoperative frozen sections have shown to result in delay of diagnosis and worse, overtreatment including orchiectomy and unnecessary chemotherapy. Therefore, primary paratesticular neuroblastoma must be considered as a differential diagnosis when evaluating and operating children with paratesticular tumors.

摘要

原发性神经母细胞瘤作为一种睾丸旁肿瘤极为罕见,全球仅报道了 8 例。本文报道了 1 例 5 月龄男婴罕见的肿瘤位置,并对目前的文献进行了更新。与我们的病例一样,这些肿瘤通常表现为 1 期疾病,单纯的肿瘤切除术可获得良好的效果和长期生存。然而,由于对此种鉴别诊断的认识不足以及术中冷冻切片的错误解读,导致诊断延迟,更糟糕的是,过度治疗包括睾丸切除术和不必要的化疗。因此,当评估和治疗睾丸旁肿瘤的儿童时,必须考虑将原发性睾丸旁神经母细胞瘤作为鉴别诊断。

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