Transanal resection of anorectal leiomyosarcoma

Pooja Venkatesh, J. Ray, E. Esen, M. Grieco, M. Bernstein
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Abstract

Anorectal leiomyosarcoma (AL) is a rare and aggressive malignancy. Although the optimal treatment of AL is unknown, surgical resection with negative margins is the mainstay of management. We describe the case of a 72-year-old woman with metastatic rectal leiomyosarcoma, who initially presented with blood per rectum and worsening constipation. She was found to have a 7 × 7.3 cm mass prolapsing through the anal canal into the perineum without extraluminal extension or pathologic lymph nodes on MRI, with pathology consistent with sarcomatoid carcinoma. Transanal R0 resection was performed. Pathology showed a 6 cm high grade sarcoma consistent with leiomyosarcoma and negative margins. Two years post-resection, the patient was found to have a metastatic flank lesion, for which she underwent surgery. If accessible transanally, radical resection of AL is a valuable approach to treatment. Evidence regarding the best adjuvant treatment strategy is lacking and should be evaluated on a case-by-case basis. Number of similar cases published: 27 articles published with 51 cases of anorectal sarcoma based on a review published in 2019.
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经肛直肠平滑肌肉瘤切除术
摘要肛门直肠平滑肌肉瘤是一种罕见且侵袭性的恶性肿瘤。虽然AL的最佳治疗方法尚不清楚,但手术切除阴性切缘是治疗的主要方法。我们描述的情况下,72岁的妇女转移性直肠平滑肌肉瘤,谁最初表现为血液每直肠和恶化便秘。MRI示一7 × 7.3 cm肿物,经肛管脱垂至会阴,无腔外延伸及病理淋巴结,病理符合肉瘤样癌。经肛门R0切除术。病理显示为6厘米高级别肉瘤,与平滑肌肉瘤一致,切缘阴性。切除两年后,患者被发现有转移性侧腹病变,为此她接受了手术。如果可以经肛门根治性切除AL是一种有价值的治疗方法。关于最佳辅助治疗策略的证据缺乏,应根据具体情况进行评估。发表的类似病例数:根据2019年发表的综述,发表了27篇文章,51例肛肠肉瘤。
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