Asynchronous tumour quadruplicity: rectosigmoid adenocarcinoma, renal cell carcinoma, prostate adenocarcinoma and neuroendocrine small-cell lung cancer - a case report.

Q4 Medicine Rozhledy v Chirurgii Pub Date : 2018-01-01
R Adwan, P Prošvic, J Prošvicová, M Tomšová
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引用次数: 0

Abstract

Introduction: Multiple tumors belong to rare cancers. Almost all malignancies may occur in combination, the most common combination being gastrointestinal cancer with respiratory or urogenital tract cancer and with breast cancer in females.

Case report: In 1999, a 66-year-old patient was diagnosed with a rectosigmoid tumor histologically proven as adenocarcinoma. Rectosigmoid resection was performed, followed by adjuvant radiotherapy and the Mayo Clinic FU/FA chemotherapy regimen. Radical nephrectomy was performed in January 2005 due to right kidney tumor, histologically detected as clear cell carcinoma. In February 2006, the patient underwent bilateral pelvic lymphadenectomy for biopsy-verified adenocarcinoma of the prostate with PSA 20.8 ng/ml. Radical prostatectomy was performed in April 2006. Histology demonstrated moderately differentiated adenocarcinoma in both prostatic lobes classified as Gleason score 4 (1+3), without invasion into the capsule or seminal vesicles infiltration. In June 2016, a native X-ray of the lungs revealed a subpleural small dense node in the right upper pulmonary field. PET/CT of the trunk was also performed showing liver metastasis and pulmonary deposits, including enlargement of the mediastinal nodules. In October 2016, liver biopsy was taken and the serum level of neuron-specific enolase (NSE: 93 ng/ml) was measured. Histology demonstrated neuroendocrine carcinoma of the small cell type. In November 2016, palliative chemotherapy with carboplatin and etoposide administered once a month was initiated. After 4 chemotherapy cycles, no deposits on the liver were detected by sonography. A native X-ray image of the lungs still showed a 15mm deposit, but NSE levels returned to normal. In March 2017, treatment continued with palliative radiotherapy of the right lung, mediastinal lymphatic nodes and prophylactic radiotherapy of the skull was planned as a next step. In August 2017, the patient died due to renal function failure and deterioration of the general condition.

Conclusion: The patient worked in uranium mines and underwent radio-chemotherapy after the first malignancy - rectosigmoid tumor. Genetic examination was not performed. The patient died of therapeutic complications of the last malignancy. Our case report does not confirm findings described so far - a shortening interval between malignancies - but confirms their increasing aggressiveness. Key words: quadruplicity - rectosigmoid adenocarcinoma - renal-cell carcinoma - prostate adenocarcinoma - neuroendocrine small-cell lung cancer.

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非同步肿瘤四联体:直肠乙状结肠腺癌、肾细胞癌、前列腺癌和神经内分泌小细胞肺癌1例报告。
简介:多发性肿瘤属于罕见的癌症。几乎所有的恶性肿瘤都可能合并发生,最常见的合并是胃肠道癌症与呼吸道或泌尿生殖道癌症以及女性乳腺癌。病例报告:1999年,一位66岁的患者被诊断为直肠乙状结肠肿瘤,组织学证实为腺癌。行乙状结肠直肠切除术,辅助放疗和梅奥诊所FU/FA化疗方案。2005年1月因右肾肿瘤行根治性肾切除术,病理检查为透明细胞癌。2006年2月,患者行双侧盆腔淋巴结切除术,活检证实为前列腺腺癌,PSA为20.8 ng/ml。2006年4月行根治性前列腺切除术。组织学示双侧前列腺叶中分化腺癌,Gleason评分4(1+3)分,未侵犯被囊或精囊浸润。2016年6月,肺x线平片示右上肺野胸膜下小致密结。躯干PET/CT显示肝转移和肺沉积,包括纵隔结节肿大。2016年10月行肝活检,测定血清神经元特异性烯醇化酶(NSE: 93 ng/ml)水平。组织学表现为小细胞型神经内分泌癌。2016年11月,开始卡铂+依托泊苷的姑息性化疗,每月1次。化疗4个周期后,超声检查未见肝脏沉积。肺部的x线图像仍然显示15mm的沉积物,但NSE水平恢复正常。2017年3月,计划继续进行右肺、纵隔淋巴结姑息性放疗和颅骨预防性放疗。2017年8月,患者因肾功能衰竭及全身状况恶化死亡。结论:该患者首次患直肠乙状结肠肿瘤后,曾在铀矿工作并接受放化疗。未进行遗传检查。病人死于最后一次恶性肿瘤的治疗并发症。我们的病例报告没有证实迄今为止所描述的发现——恶性肿瘤之间的间隔缩短——但证实了它们的侵袭性越来越强。关键词:四肢-直肠乙状结肠腺癌-肾细胞癌-前列腺癌-神经内分泌小细胞肺癌
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来源期刊
Rozhledy v Chirurgii
Rozhledy v Chirurgii Medicine-Medicine (all)
CiteScore
0.50
自引率
0.00%
发文量
67
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