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上尿路局部晚期淋巴上皮瘤样癌的八年随访:一例报告

Eight-year follow-up of locally advanced lymphoepithelioma-like carcinoma at upper urinary tract: A case report.

作者信息

Yang Che H, Weng Wei C, Lin Yi S, Huang Li H, Lu Chin H, Hsu Chao Y, Ou Yen C, Tung Min C

机构信息

Department of Surgery, Division of Urology, Tungs' Taichung MetroHarbor Hospital, Taichung City 435403, Taiwan.

出版信息

World J Clin Cases. 2020 Oct 6;8(19):4505-4511. doi: 10.12998/wjcc.v8.i19.4505.

Abstract

BACKGROUND

Urinary tract lymphoepithelioma-like carcinoma is rarely seen. Although it is termed after lymphoepithelioma at the nasopharynx, it behaves more like high grade urothelial carcinoma by immunohistochemical features. Most published literatures focused on its rarity but few discussed results of long-term follow-ups. As no available guidelines are applicable, we postulated that principles should be similar to that of urothelial carcinoma at urinary tract. As of now, this work features the longest follow-up of this cancer at the upper urinary tract.

CASE SUMMARY

A 63-year-old female had a chief complaint of intermittent left flank pain for 2 mo, along with accompanying symptoms including vomiting and body weight loss, about 7 kg over 2 mo. Laboratory data showed normocytic anemia, mildly poor renal function, and hyperparathyroidism. Urine analysis showed mild hematuria. Computed tomography showed a 4.2-cm-width irregular mass over left renal pelvic and enlarged lymph node at the left renal hilum. Whole-body bone scan was negative of active bone lesions. Biopsy from ureteroscopy showed urothelial carcinoma. Specimen from laparoscopic nephroureterectomy with bladder cuff resection showed lymphoepithelioma-like carcinoma with muscular invasion (pT3). She took adjuvant chemotherapies of 2 cycles and full courses of radiation therapy. No recurrence was observed with designed investigative programs.

CONCLUSION

Locally advanced urinary tract lymphoepithelioma-like carcinoma could benefit from nephroureterectomy and bladder cuff excision in terms of recurrence-free survival.

摘要

背景

尿路淋巴上皮瘤样癌较为罕见。尽管它因鼻咽部的淋巴上皮瘤而得名,但通过免疫组化特征显示其行为更类似于高级别尿路上皮癌。大多数已发表的文献聚焦于其罕见性,而很少讨论长期随访结果。由于没有适用的指南,我们推测其治疗原则应与尿路尿路上皮癌相似。截至目前,这项工作是对上尿路该癌症最长时间的随访。

病例摘要

一名63岁女性,主要症状为间歇性左侧腰痛2个月,伴有呕吐和体重减轻等伴随症状,2个月内体重减轻约7千克。实验室检查显示正细胞性贫血、轻度肾功能不全和甲状旁腺功能亢进。尿液分析显示轻度血尿。计算机断层扫描显示左肾盂有一个4.2厘米宽的不规则肿块,左肾门淋巴结肿大。全身骨扫描未发现活动性骨病变。输尿管镜活检显示为尿路上皮癌。腹腔镜肾输尿管切除术加膀胱袖状切除术标本显示为伴有肌层浸润的淋巴上皮瘤样癌(pT3)。她接受了2个周期的辅助化疗和全程放疗。按照设计的检查方案未观察到复发。

结论

就无复发生存而言,局部晚期尿路淋巴上皮瘤样癌可从肾输尿管切除术和膀胱袖状切除术中获益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f19c/7559648/1c697ab92ada/WJCC-8-4505-g001.jpg

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