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Case Report: Leiomyosarcoma: a rare sinonasal malignancy

机译:病例报告:平滑肌肉瘤:一种罕见的鼻窦恶性肿瘤

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摘要

Leiomyosarcomas (LMS) are rare sinonasal malignant tumours with 20 cases of nasal LMS previously reported in the literature. An 81-year-old man presented with an incidental left nasal lesion associated with left nasal obstruction and occasional left-sided blood-stained rhinorrhoea. Nasendoscopic examination showed green coloured polyps filling the left nasal cavity with biopsies showing LMS. CT imaging did not show any bony erosion. No metastases were found on positron emission tomography imaging. The patient underwent endoscopic resection and all surgical margins were clear of disease. The patient was declined postoperative radiotherapy, and serial follow-up has not shown any recurrence to date. Nasal LMS are rare sinonasal smooth muscle tumours and symptoms and radiological findings are often non-specific. Therefore, diagnosis is made on histopathological and immunohistochemical analysis. Due to their invasive nature, the treatment of choice is complete surgical resection, with adjuvant therapy reserved for patients with locally advanced or metastatic disease.
机译:平滑肌肉瘤(LMS)是罕见的鼻窦恶性肿瘤,以前文献报道有20例鼻LMS。一名81岁的男子出现左鼻偶发性病变,伴有左鼻阻塞和偶发的左侧染有血性鼻涕。鼻镜检查显示绿色息肉充满左鼻腔活检显示LMS。 CT成像未显示任何骨侵蚀。在正电子发射断层扫描成像中未发现转移。该患者接受了内窥镜切除术,所有手术切缘均无疾病。该患者术后放射治疗被拒绝,并且迄今连续随访未显示任何复发。鼻LMS是罕见的鼻窦平滑肌肿瘤,其症状和影像学检查结果通常不是特异性的。因此,对组织病理学和免疫组织化学分析进行诊断。由于其侵袭性,选择的治疗方法是完全手术切除,并为局部晚期或转移性疾病患者保留辅助治疗。

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