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Giant retroperitoneal liposarcoma: A case report and literature review

机译:巨大腹膜后脂肪肉瘤:一例报告并文献复习

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摘要

Retroperitoneal liposarcomas are a heterogeneous group of mesenchymal tumours that have a wide spectrum of histological subtypes and vague clinical presentations. Herein, we present the case of a 75-year-old man with anorexia, weight loss of 7 kg, and a growing abdominal circumference within a span of 6 weeks. Computed tomography of the abdomen and pelvis showed a large mass that filled almost the entire abdominal cavity. After consultation with a multidisciplinary tumour board, en bloc resection of the tumour was performed. In addition, the left kidney and a part of the left diaphragm were removed. The tumour measured 35 × 29 × 20.5 cm and weighed 11.6 kg. The histological report confirmed low-grade dedifferentiated liposarcoma with scarce atypical adipocytes, lipoblasts containing spindle cell, pleomorphic, and chondroid components. The patient had uneventful recovery and remained stable during the follow-up period. We report this case to highlight the need for customized surgical oncological measures in the treatment of solid abdominal tumours due to locoregional invasion that usually necessitates en bloc resection.
机译:腹膜后脂肪肉瘤是间质性肿瘤的异质性组,具有广泛的组织学亚型和模糊的临床表现。在此,我们介绍了一个75岁的男性患者的厌食,体重减轻7公斤,腹围在6周内不断增长的情况。腹部和骨盆的计算机断层扫描显示肿块几乎充满整个腹腔。与多学科肿瘤委员会协商后,进行肿瘤整体切除。另外,左肾和左diaphragm膜的一部分被去除。肿瘤尺寸为35×29×20.5cm,重11.6kg。组织学报告证实,低级去分化脂肪肉瘤具有稀疏的非典型脂肪细胞,含有梭形细胞的脂母细胞,多形性和软骨样成分。该患者恢复平稳,在随访期间保持稳定。我们报告此病例以强调因局部区域浸润而通常需要整块切除的实体腹部肿瘤的治疗中需要定制的手术肿瘤学措施。

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