A rare case of intrascrotal lipoblastoma in a 2-year-old: Case report and literature review

IF 0.5 Q4 UROLOGY & NEPHROLOGY
Fawaz Alkeraithe , Yazeed Alghtani , Subhy Abo Rubeea , Mutasim Alkhalifah , Majed Alenzi , Abdulaziz Alhussain
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引用次数: 0

Abstract

Lipoblastomas are rare benign tumors arising from embryonal fat tissues, commonly occurring in early childhood. Scrotal presentation is exceedingly rare, with 18 cases reported in the literature. We present a 2-year-old male with a 5-month history of painless scrotal swelling, initially suspected of being malignant. Imaging suggested the possibility of atypical lipoma. The patient underwent orchiectomy. Histopathologic examination confirmed the diagnosis of lipoblastoma, with no MDM2 amplification. After two years of follow-up, the patient remains recurrence-free. This case highlights the challenges of diagnosing pediatric scrotal masses preoperatively and highlights the importance of a multidisciplinary approach for accurate diagnosis and management.
2岁儿童腹壁内脂肪母细胞瘤1例:病例报告及文献复习
脂肪母细胞瘤是一种罕见的良性肿瘤,起源于胚胎脂肪组织,常见于儿童早期。阴囊表现极为罕见,文献报道有18例。我们报告一名2岁男性,有5个月的无痛性阴囊肿胀史,最初怀疑是恶性的。影像学提示可能为非典型脂肪瘤。病人接受了睾丸切除术。组织病理学检查证实为脂肪母细胞瘤,未见MDM2扩增。经过两年的随访,患者没有复发。本病例强调了儿科阴囊肿块术前诊断的挑战,并强调了多学科方法对准确诊断和管理的重要性。
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
Urology Case Reports
Urology Case Reports Medicine-Urology
CiteScore
0.90
自引率
20.00%
发文量
325
审稿时长
37 days
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