Retroperitoneal Liposarcoma: The Giant Type.

Journal of Medical Cases Pub Date : 2022-10-01 Epub Date: 2022-10-31 DOI:10.14740/jmc4014
Subhi Mansour, Nassim Azzam, Yoram Kluger, Safi Khuri
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引用次数: 1

Abstract

Retroperitoneal tumors (RPTs) are very rare tumors that arise in the large space of the retroperitoneum. About two-third of these tumors are malignant, of which soft tissue sarcoma (STS) is the most common and comprises almost one-third of malignant RPTs. Twenty to thirty percent of RPTs are benign. The retroperitoneal cavity has a very large potential space for tumor enlargement to a very high diameters without causing specific symptoms, especially during the initial phase of tumor enlargement. On diagnosis, the average tumor weight is 15 - 20 kg and tumor diameter is 20 - 25 cm. The most common retroperitoneal sarcoma type is liposarcoma, which account for 20% of all sarcoma types and 40% of all retroperitoneal sarcomas (RPSs). Other less common STS arise in the retroperitoneum include leiomyosarcoma and undifferentiated pleomorphic type. Giant liposarcoma is usually defined either as tumor diameter of 30 cm or more or tumor weight of 20 kg or higher. This specific type of sarcoma is very uncommon, with few case reports published in the English literature. Herein, we present a case of a healthy 33-year-old male patient, who was admitted due to abdominal distension and increased body weight since few months. An abdominopelvic computed tomography (CT) scan demonstrated a giant retroperitoneal mass of almost 40 cm in diameter in its largest dimension, located in the right retroperitoneal space. Ultrasound (US)-guided fine needle biopsy (FNB) was consistent with well differentiated liposarcoma. Surgical resection of the tumor along with the right colon, right ureter and kidney, third and fourth duodenal parts and part of the right iliopsoas muscle was contemplated. Histopathological report revealed well-differentiated liposarcoma of 50 cm in diameter, with foci of dedifferentiation, presented by pleomorphic sarcoma. Surgical margins were microscopically negative.

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腹膜后脂肪肉瘤:巨型型。
腹膜后肿瘤(RPTs)是非常罕见的肿瘤,发生在腹膜后的大空间。这些肿瘤中约有三分之二是恶性的,其中软组织肉瘤(STS)最为常见,占恶性rpt的近三分之一。20%到30%的rpt是良性的。腹膜后腔有很大的潜在空间使肿瘤扩大到非常大的直径,而不会引起特定的症状,特别是在肿瘤扩大的初期。诊断时,肿瘤平均重量为15 - 20公斤,肿瘤直径为20 - 25厘米。最常见的腹膜后肉瘤类型是脂肪肉瘤,占所有肉瘤类型的20%,占所有腹膜后肉瘤(rps)的40%。其他不常见的发生在腹膜后的STS包括平滑肌肉瘤和未分化多形性。巨大脂肪肉瘤通常定义为肿瘤直径大于或等于30cm,或肿瘤重量大于或等于20kg。这种特殊类型的肉瘤非常罕见,在英语文献中很少有病例报告。在此,我们报告一位健康的33岁男性患者,因腹胀和体重增加几个月而入院。腹部骨盆计算机断层扫描(CT)显示一个巨大的腹膜后肿块,最大直径约40厘米,位于右侧腹膜后间隙。超声引导下细针活检(FNB)符合高分化脂肪肉瘤。考虑将肿瘤连同右结肠、右输尿管、右肾、十二指肠第三、第四部分及部分右髂腰肌一并切除。组织病理学报告显示直径50厘米的高分化脂肪肉瘤,伴有去分化灶,表现为多形性肉瘤。手术缘镜下呈阴性。
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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