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乙状结肠系膜去分化脂肪肉瘤——病例报告

Dedifferentiated Liposarcoma of Sigmoid Mesocolon - A Case Report.

作者信息

Constantinoiu Silviu, Achim Ion-Florin, Cretu Oana-Eliza, Dumitru Tatiana, Constantin Adrian, Enache Simona, Mates Ioan Nicolae

出版信息

Chirurgia (Bucur). 2016 Jul-Aug;111(4):330-6.

Abstract

Dedifferentiated liposarcoma is a liposarcoma that contains a well-differentiated liposarcoma component juxtaposed to areas of high-grade non-lipogenic sarcoma and was believed to occur from well-differentiated liposarcoma after several years. Dedifferentiated liposarcoma most commonly occurs in the retroperitoneum, while an intraperitoneal location is extremely rare, only seven cases have been reported in literature. Many pathologists recognize that a large number of intra-abdominal poorly differentiated sarcomas are dedifferentiated liposarcomas. We present the case of a 73 years old patient known with multiple cardiovascular comorbidities, stroke sequelae and a large abdominal mass evolving for 3 years. He was referred to our clinic for abdominal pain and bowel disorders. Instead of all clinical and imagistic aspects suggested a gastrointestinal stromal tumour, the histological exam revealed the diagnosis of a dedifferentiated liposarcoma.

摘要

去分化脂肪肉瘤是一种脂肪肉瘤,它包含一个与高级别非脂肪生成性肉瘤区域并列的高分化脂肪肉瘤成分,并且被认为是在数年后由高分化脂肪肉瘤演变而来。去分化脂肪肉瘤最常发生于腹膜后,而发生于腹腔内的情况极为罕见,文献中仅报道过7例。许多病理学家认识到,大量腹腔内低分化肉瘤是去分化脂肪肉瘤。我们报告一例73岁患者,该患者患有多种心血管合并症、中风后遗症,并有一个已存在3年的腹部巨大肿块。他因腹痛和肠道疾病转诊至我们的诊所。尽管所有临床和影像学表现均提示为胃肠道间质瘤,但组织学检查确诊为去分化脂肪肉瘤。

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