Recurrence Leiomyosarcoma of the Popliteal Vein: A Rare Soft Tissue Sarcoma.

IF 0.6 Q4 SURGERY Case Reports in Surgery Pub Date : 2023-02-16 eCollection Date: 2023-01-01 DOI:10.1155/2023/2788584
Thanate Poosiripinyo, Sermsak Sukpanichyingyong, Krits Salang, Chat Sumananont, Thanapon Chobpenthai
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Abstract

Background: Leiomyosarcoma (LMS) is a soft tissue sarcoma that originates from smooth muscle cells and constitutes approximately 5-10% of all soft tissue sarcomas. Vascular LMS is the least common subtype of LMS. About one-third of vascular LMS is located in the extremities, most commonly in the saphenous vein (25%). Vascular LMS originating from the popliteal vein is very rare, and to the best of our knowledge, only nine cases have been reported to date. Case presentation. We herein report a case of a 49-year-old woman who presented with recurrence of a mass that was located at the posterior aspect of the right proximal leg and extended to the popliteal fossa. She had mild pain and intermittent claudication without a history of an edematous leg. The tissue diagnosis was LMS. Wide en bloc resection of the tumor, including the segment of the involved popliteal vein, was performed without venous reconstruction. The patient received no other adjuvant treatments. At the 16-month follow-up, she had good oncologic and functional outcomes.

Conclusion: Vascular LMS at the popliteal vein is uncommon but should be considered as a differential diagnosis in a patient who presents with a mass at the popliteal fossa. The magnetic resonance imaging (MRI) and core needle biopsy were needed for a definite diagnosis. The mainstay of treatment is wide en bloc resection of the tumor, including the involved segment of the vein. Venous reconstruction after resection is unnecessary in chronic cases without a history of an edematous leg. Radiotherapy is an important adjuvant for local control when the surgical margins are close or positive. The role of chemotherapy in systemic management remains unclear.

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腘静脉雷米肉瘤复发:一种罕见的软组织肉瘤
背景:平滑肌肉瘤(LMS)是一种起源于平滑肌细胞的软组织肉瘤,约占所有软组织肉瘤的 5-10%。血管型LMS是LMS中最不常见的亚型。约三分之一的血管性 LMS 位于四肢,最常见的是大隐静脉(25%)。起源于腘静脉的血管性 LMS 非常罕见,据我们所知,迄今为止仅有九例报道。病例介绍。我们在此报告了一例 49 岁女性的病例,她的右腿近端后侧肿块复发并延伸至腘窝。她有轻微疼痛和间歇性跛行,没有腿部水肿病史。组织诊断为 LMS。对肿瘤进行了大范围全切,包括受累的腘静脉,但未进行静脉重建。患者没有接受其他辅助治疗。在16个月的随访中,她的肿瘤和功能状况良好:结论:腘静脉血管性 LMS 并不常见,但应作为腘窝肿块患者的鉴别诊断。确诊需要进行磁共振成像(MRI)和核心针活检。治疗的主要方法是对肿瘤进行大范围整体切除,包括受累的静脉段。对于没有水肿腿病史的慢性病例,切除后无需进行静脉重建。当手术切缘接近或呈阳性时,放疗是局部控制的重要辅助手段。化疗在全身治疗中的作用仍不明确。
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