Myxoid liposarcoma diagnosed on fine needle aspiration cytology: There is more to it than meets the eye.

Md Ali Osama, Priti Chatterjee, Smita Singh, Ankita Pandey, Anup Mohta
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Abstract

Abstract: Liposarcoma is a rare mesenchymal neoplasm commonly involving deep soft tissues and the retroperitoneum. Among the various types of liposarcoma, myxoid liposarcoma is the most frequently encountered in adolescents and young adults, with a predilection for lower extremities. Fine needle aspiration allows easy assessment and rapid on-site evaluation for distinguishing benign from malignant lipomatous lesions. Here, we present a case of myxoid liposarcoma in the calf region of a 19-year-old boy, diagnosed via fine needle aspiration cytology, and subsequently confirmed by histopathological examination after surgical resection. The intention behind this case report is to highlight the cytological features of myxoid liposarcoma and to improve understanding of this tumor entity, aiming to prevent misdiagnosis by inexperienced pathologists when evaluating cytology specimens.

细针穿刺细胞学诊断为肌样脂肪肉瘤:它比我们看到的要复杂得多。
摘要:脂肪肉瘤是一种罕见的间叶肿瘤,通常累及深部软组织和腹膜后。在各种类型的脂肪肉瘤中,肌样脂肪肉瘤最常见于青少年和年轻成年人,且好发于下肢。细针穿刺术便于评估和现场快速评价,可区分良性和恶性脂肪瘤病变。在此,我们介绍了一例 19 岁男孩小腿部位的类肌脂肪肉瘤病例,该病例通过细针穿刺细胞学检查确诊,随后在手术切除后经组织病理学检查确诊。本病例报告旨在强调肌样脂肪肉瘤的细胞学特征,加深人们对这一肿瘤实体的认识,从而避免经验不足的病理学家在评估细胞学标本时误诊。
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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