The Adipocerous Ossein- Chondroid Lipoma

Anu Bajaj
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Abstract

Mesenchymal soft tissue adipocytic neoplasms are frequently discerned tumors demonstrating diverse histological subcategories. Chondroid lipoma is an extremely exceptional, benign adipocytic neoplasm initially scripted by Meis and Enzinger in 1993 as a tumefaction simulating liposarcoma or myxoid chondrosarcoma [1]. As the neoplasm is composed of mature adipocytes, lipoblasts and myxochondroid stroma, chondroid lipoma may be histologically misinterpreted as an adipose tissue sarcoma, round cell liposarcoma or extra-skeletal myxoid chondrosarcoma. As malignant tumours are therapeutically managed with adjuvant radiotherapy, chemotherapy, and extensive surgical resection wherein benign tumours are appropriately addressed by marginal resection, cogent distinction between benign lipomatous neoplasms from diverse malignant neoplasms is necessitated to circumvent unnecessary therapeutic intervention and associated adverse outcomes. The essentially benign chondroid lipoma does not mandate expansive surgical extermination, adjunctive radiotherapy, or chemotherapy.
脂质骨胶原-软骨样脂肪瘤
间充质软组织脂肪细胞瘤是一种常见的肿瘤,具有不同的组织学亚类。软骨样脂肪瘤是一种极为罕见的良性脂肪细胞肿瘤,最初由Meis和Enzinger于1993年将其描述为一种类似脂肪肉瘤或黏液样软骨肉瘤的肿瘤[1]。由于肿瘤由成熟脂肪细胞、脂肪母细胞和黏液软骨样基质组成,软骨样脂肪瘤在组织学上可能被误解为脂肪组织肉瘤、圆细胞脂肪肉瘤或骨外黏液样软骨肉瘤。由于恶性肿瘤的治疗是通过辅助放疗、化疗和广泛的手术切除来进行的,其中良性肿瘤通过边缘切除得到适当的治疗,因此有必要将良性脂肪瘤与各种恶性肿瘤进行明确区分,以避免不必要的治疗干预和相关的不良后果。本质上良性的软骨样脂肪瘤不需要广泛的手术切除、辅助放疗或化疗。
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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