Dedifferentiated recurrent liposarcoma of the uterine corpus: A case report and literature review

IF 0.7 Q4 OBSTETRICS & GYNECOLOGY Case Reports in Women's Health Pub Date : 2024-12-01 DOI:10.1016/j.crwh.2024.e00670
Sana Mushtaq , Muhammad Arslan Ul Hassan , Yan Li , Ikran Abdi , Aqsa Ahmad , HaiNing Li
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Abstract

Liposarcoma of the uterine corpus represents an exceptionally rare tumor, with few cases documented in the literature, underscoring its unique histopathologic characteristics and management challenges. This case describes the clinical management of a 57-year-old patient with well-differentiated liposarcoma of the uterine corpus who presented with a three-month history of abdominal pain and distension. She underwent an abdominal hysterectomy followed by chemotherapy but experienced local recurrence in the mesentery and retroperitoneum after 21 months. Tumor resection was performed again, followed by chemotherapy, but the patient experienced a second recurrence 15 months later, involving the small intestine, vaginal stump, and ureter, with evidence of dedifferentiated liposarcoma. A third surgical resection was carried out without administering chemotherapy and the patient remained asymptomatic at follow-up appointments every 3 months for a year. This case highlights the importance of acknowledging the aggressive nature of recurrent liposarcoma, especially its transition into dedifferentiated liposarcoma, and the need for tailored management strategies.
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子宫体去分化复发性脂肪肉瘤1例报告并文献复习
子宫体脂肪肉瘤是一种非常罕见的肿瘤,文献中记录的病例很少,强调了其独特的组织病理学特征和治疗挑战。本病例描述了一名57岁的子宫体高分化脂肪肉瘤患者的临床处理,该患者表现为三个月的腹痛和腹胀史。她接受了腹部子宫切除术和化疗,但在21个月后肠系膜和腹膜后局部复发。再次行肿瘤切除术,随后化疗,但患者在15个月后第二次复发,累及小肠、阴道残端和输尿管,并伴有去分化脂肪肉瘤的证据。第三次手术切除未进行化疗,患者在随访中每3个月无症状,持续一年。这个病例强调了认识到复发性脂肪肉瘤侵袭性的重要性,特别是它向去分化脂肪肉瘤的转变,以及需要量身定制的管理策略。
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来源期刊
Case Reports in Women's Health
Case Reports in Women's Health Medicine-Obstetrics and Gynecology
CiteScore
2.10
自引率
0.00%
发文量
89
审稿时长
7 days
期刊最新文献
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