具有多形性特征的浅表非典型脂肪瘤:病例报告与文献讨论

Oluwaseyi Adeuyan, Emily R. Gordon, Brigit A. Lapolla, Celine M. Schreidah, V. Jobanputra, Alejandro A. Gru, L. J. Geskin
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引用次数: 0

摘要

在脂肪肉瘤中,分化良好的脂肪肉瘤和脱分化脂肪肉瘤最为常见。这些肿瘤大多发生在腹膜后深部或四肢。在腹膜后以外的部位发现的脂肪源性肿瘤被称为非典型脂肪瘤(ALT)。浅表性脂肪瘤尤其罕见,因此人们对其临床表现、基因组状态和治疗方法知之甚少。在此,我们介绍了一例 54 岁男性的病例,他的左上背部有一个间歇性的、缓慢生长的肿块,已经持续了两年多,被偶然诊断为 ALT。然而,与文献中描述的大多数其他 ALT 不同的是,该患者的 ALT 表现出高度多形性,伴有 MDM2 和对照中心粒 12(CEP12)共扩增,CD34、S100 和 RB1 表达阴性。本病例报告详细介绍了脂肪瘤的诊断方法和组织病理学结果,总结了不同的亚型,包括非典型纺锤形细胞/多形性脂肪瘤、多形性脂肪肉瘤和纺锤形细胞/多形性脂肪瘤,并简要讨论了处理方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Superficial Atypical Lipomatous Tumor With Pleomorphic Features: Case Report and Discussion of the Literature
Among liposarcomas, well-differentiated liposarcoma and dedifferentiated liposarcoma are the most common. The majority of these tumors are found in deep retroperitoneum or extremities. When found outside the retroperitoneum, these adipose-derived tumors are known as atypical lipomatous tumors (ALT). Superficial ALT are particularly rare; thus, little is known about their clinical presentation, genomic status, and management. Here, we present the case of a 54-year-old man with an intermittently bothersome, slowly growing mass on his left upper back for over 2 years, which was incidentally diagnosed as ALT. This patient's ALT, however, showed a profound degree of pleomorphism with MDM2 and control centromere 12 (CEP12) coamplification and negative CD34 and S100 and RB1 expression, unlike most other ALT described in the literature. This case report details the diagnostic workup and histopathological findings for adipose tumors and summarizes the different subtypes, including atypical spindle cell/pleomorphic lipomatous tumor, pleomorphic liposarcoma, and spindle cell/pleomorphic lipoma, with brief discussion on management.
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