成人原发性肾横纹肌肉瘤伴局部复发及肝转移1例报告

IF 1.9 Q3 ONCOLOGY Journal of Kidney Cancer and VHL Pub Date : 2022-04-14 DOI:10.15586/jkcvhl.v9i1.218
H. Nasrollahi, Ali Eslahi, Ali Ariafar, F. Ahmed, A. Monabati
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引用次数: 1

摘要

原发性肾横纹肌肉瘤(RMS)在成人中是罕见的,只有少数病例在文献中发表。它是一种具有侵袭性和快速临床进展过程的间充质肿瘤。我们提出了一个58岁的女性原发性肾RMS病例,她在过去的一年里出现了间歇性腹痛。计算机断层扫描(CT)显示一个20×25×8厘米的不均匀实性肿块,在中极延伸到右肾下极。因此,患者接受了右侧肾输尿管根治术。组织病理学检查和免疫组织化学研究证实了RMS具有多形性成分的诊断。术后,患者出院,无任何并发症,并被转介到肿瘤科医生化疗。然而,2个月的随访CT扫描显示广泛的肝转移和局部复发。患者接受吉西他滨和多西他赛治疗,但病情恶化,5个月后去世。原发性肾RMS在成人中很少见。此外,肝转移并不常见,对其了解甚少。因此,我们描述了临床病理特征,包括我们病例的临床随访,重点是疾病进展,治疗和结果。
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Primary Rhabdomyosarcoma of Kidney with Local Recurrence and Liver Metastasis in Adults: A Case Report
Primary rhabdomyosarcoma (RMS) of the kidney in an adult is rare, with only a few cases published in the literature. It is a mesenchymal tumor associated with an aggressive and rapid clinical progression course. We present a case of primary renal RMS in a 58-year-old female who presented with intermittent abdominal pain in the past year. The computed tomography (CT) scan revealed a 20×25×8 cm heterogeneous solid mass in the middle pole extended to the lower pole of the right kidney. Therefore, the patient underwent a right radical nephroureterectomy. Histopathology examination and immunohistochemistry studies confirmed the diagnosis of RMS with pleomorphic components. Postoperatively, the patient was discharged without any complications and was referred to an oncologist for chemotherapy. However, a follow-up CT scan in 2 months showed widespread liver metastasis and local recurrence. The patient received Gemcitabine and Docetaxel, but her condition worsened, and she passed away 5 months later. Primary renal RMS is rare in adults. In addition, liver metastasis is uncommon and poorly understood. Hence, we describe the clinicopathologic characteristics, including clinical follow-up of our case, focusing on the disease progression, treatment, and outcome.
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来源期刊
自引率
6.20%
发文量
22
审稿时长
4 weeks
期刊最新文献
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