肾脏原发性良性肉瘤并转移至对侧肾脏。病例报告。

Q2 Medicine
Sergio Vasquez Ciriaco, Jaime Aron García Espinoza, Elena Enselmini Garcia Pedro
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引用次数: 0

摘要

导言:肾脏良性肉瘤是世界上罕见的肿瘤,人们对它的认识主要基于各种报道和病例;然而,由于其恶性潜能和平均 18 个月的存活期,其预后是暗淡的:临床病例:一名 54 岁女性,临床表现为右侧腹部疼痛 6 个月,断层扫描图像显示双侧肾脏病变,接受了右侧根治性肾切除术和左侧保守性手术。最终的组织病理学检查报告为右侧原发性肾脏细肌瘤伴左侧转移:结论:肾细肌肉瘤是一种发病率低、死亡率高的实体肿瘤;然而,我们的病例在文献报道的对侧肾脏转移患者中占少数。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Primary leiomyosarcoma of kidney with metastasis to contralateral kidney. Case report.

Primary leiomyosarcoma of kidney with metastasis to contralateral kidney. Case report.

Primary leiomyosarcoma of kidney with metastasis to contralateral kidney. Case report.

Primary leiomyosarcoma of kidney with metastasis to contralateral kidney. Case report.

Introduction: Renal leiomyosarcoma is a rare entity in the world and its understanding is based on reports and various cases; however, the prognosis is bleak for its malignant potential and an average survival of 18 months.

Clinical case: A 54-year-old woman with a clinical picture of 6 months of pain in the right flank and a tomographic image of a bilateral renal lesion underwent right radical nephrectomy and left conservative surgery. The definitive histopathological study reported right primary renal leiomyosarcoma with left metastasis.

Conclusion: Renal leiomyosarcoma is an entity of low incidence and high mortality; however, our case represents the minority of patients with contralateral kidney metastasis reported in the literature.

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来源期刊
Interventional Medicine and Applied Science
Interventional Medicine and Applied Science MEDICINE, GENERAL & INTERNAL-
CiteScore
1.60
自引率
0.00%
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审稿时长
15 weeks
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