Paratesticular Dedifferentiated Liposarcoma with Rhabdomyoblastic Differentiation: A Case Report and Review of the Literature.

Q4 Biochemistry, Genetics and Molecular Biology
Ahmet Keles, Ozgur Arikan, Ferhat Keser, Ayse Nur Toksoz Yildirim, Asif Yildirim
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引用次数: 0

Abstract

Liposarcomas of the paratesticular tissue is a rare pathological entity. The symptoms are similar to inguinal hernias or hydroceles. We present the case of an 84-year-old man with a rare paratesticular liposarcoma that manifested as painless right hemiscrotal swelling. Testicular tumour markers were negative. Imaging revealed a heterogeneous mass with a fat component. He underwent a radical orchiectomy on the left side to remove the associated mass. This revealed dedifferentiated liposarcoma (DDLS) with rhabdomyoblastic differentiation and MDM2 amplification. The surgical margins were negative, and the patient had a metastatic workup that included magnetic resonance imaging (MRI) of the abdomen and pelvis. Because of the disease's rarity, there is no clear agreement on radiotherapy and chemotherapy roles.

伴横纹肌母细胞分化的睾丸旁低分化脂肪肉瘤:病例报告和文献综述。
睾丸旁组织脂肪肉瘤是一种罕见的病理实体。其症状与腹股沟疝或鞘膜积液相似。本病例是一名84岁的男性,患有罕见的睾丸旁脂肪肉瘤,表现为右半阴囊无痛性肿胀。睾丸肿瘤标志物呈阴性。影像学检查显示肿块为脂肪成分的异质性肿块。他接受了左侧睾丸根治性切除术,切除了相关肿块。术中发现了具有横纹肌母细胞分化和MDM2扩增的脂肪肉瘤(DDLS)。手术切缘为阴性,患者接受了包括腹部和盆腔磁共振成像(MRI)在内的转移性检查。由于这种疾病非常罕见,目前对放疗和化疗的作用还没有明确的共识。
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
Prague medical report
Prague medical report Medicine-Medicine (all)
CiteScore
1.10
自引率
0.00%
发文量
19
审稿时长
20 weeks
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