Primary renal well-differentiated neuroendocrine tumors with lymph node metastasis: A case report and literature review

Q4 Medicine
Huy-Hoang Nguyen, Hoang-Giang Phan, Duc-Thuong Ho, Van-Hung Le
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引用次数: 0

Abstract

Introduction

Well-differentiated neuroendocrine tumors of the kidney are rare and generally less aggressive than renal cell carcinoma, although metastasis is still present at the time of diagnosis. Surgical resection remains the preferred treatment, even in cases with lymph node metastases.

Case presentation

We present the case of a 38-year-old female with a right renal WDNET and lymph node metastasis who underwent laparoscopic radical nephrectomy with lymphadenectomy. Pathological examination confirmed metastasis in 9 out of 11 lymph nodes. Immunohistochemistry results were positive for synaptophysin and chromogranin, with a Ki-67 index of less than 10%. No recurrence was observed after 36 months.

Conclusion

Well-differentiated neuroendocrine tumors are rare, with non-specific clinical and imaging characteristics, requiring immunohistochemical analysis for diagnosis. Surgical resection is the treatment of choice, and long-term follow-up is essential.

Abstract Image

原发性肾高分化神经内分泌肿瘤伴淋巴结转移1例并文献复习
肾的高分化神经内分泌肿瘤是罕见的,通常不如肾细胞癌侵袭性强,尽管在诊断时仍然存在转移。手术切除仍然是首选的治疗方法,即使在淋巴结转移的情况下。我们报告一例38岁的女性右肾WDNET和淋巴结转移的病例,她接受了腹腔镜根治性肾切除术和淋巴结切除术。病理检查证实11个淋巴结中有9个转移。免疫组化结果synaptophysin、chromogranin阳性,Ki-67指数< 10%。36个月后无复发。结论高分化神经内分泌肿瘤罕见,临床及影像学特征无特异性,需要免疫组化分析诊断。手术切除是治疗的选择,长期随访是必要的。
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来源期刊
IJU Case Reports
IJU Case Reports Medicine-Urology
CiteScore
0.60
自引率
0.00%
发文量
147
审稿时长
15 weeks
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