Pleomorphic lipoma: A gentle giant of pathology

Uma Sakhadeo, Rajesh Mundhe, M. Desouza, R. Chinoy
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引用次数: 11

Abstract

Pleomorphic lipoma is a relatively rare adipocytic neoplasm, occurring predominantly in elderly males in the subcutaneous tissues of the neck or shoulder. To the best of our knowledge, only five cases have been reported in which the lesion was intramuscular. We hereby report a case of a 60-year-old female patient, presenting with an intramuscular, posterior shoulder mass. The aspirate showed a giant cell-rich lesion, admixed with short, plump-looking, spindly cells. There was no overt evidence of malignancy; however, the cell cytology was sufficiently atypical to warrant concern. Subsequent excision revealed a classical pleomorphic lipoma on histology with no evidence of malignancy. CD34 staining by immunohistochemistry further supported the diagnosis. Differential diagnosis and the cytological diagnostic pitfalls of pleomorphic lipomas have been discussed with a review of the literature.
多形性脂肪瘤:一个温和的病理巨人
多形性脂肪瘤是一种相对罕见的脂肪细胞肿瘤,主要发生于老年男性颈部或肩部的皮下组织。据我们所知,只有5例报告病变是在肌肉内。我们在此报告一例60岁的女性患者,表现为肌肉内,肩部后部肿块。抽吸显示一个巨细胞丰富的病变,夹杂着短的、丰满的、细长的细胞。没有明显的恶性肿瘤证据;然而,细胞细胞学表现不典型,值得关注。随后的切除在组织学上显示为典型的多形性脂肪瘤,没有恶性肿瘤的证据。免疫组织化学CD34染色进一步支持诊断。本文对多形性脂肪瘤的鉴别诊断和细胞学诊断缺陷进行了讨论,并对文献进行了回顾。
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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