Feng Yuhua, Zhong Meizuo, Zeng Shan, Xiao Desheng, Liu Yiping
Department of Oncology Department of Pathology, Xiangya Hospital, Central South University, Changsha, Hunan Province, People's Republic of China.
Medicine (Baltimore). 2018 Jun;97(26):e11332. doi: 10.1097/MD.0000000000011332.
Multiple primary neoplasms (MPNs) are rare. Most MPNs are double, and triple primary neoplasms are extremely rarer. Here, we describe a case of a 66-year-old man diagnosed with metachronous triple primary neoplasms with primary prostate cancer, lung cancer and colon cancer.
The patient complained of dysuria in January 2015, and he underwent transurethral resection of the prostate. The pathological results showed acinar adenocarcinoma of prostate with a Gleason score of 3+3. In January 2017, he complained of lower abdominal pain, then he took an enteroscopy examination, found a mass in the sigmoid colon, and positron emission tomography/computed tomography examination showed masses in the sigmoid colon and right upper lobe of the lung. Biopsy of the colon showed moderately differentiated adenocarcinoma with Kirsten rat sarcoma viral oncogene homolog exon 2 mutation, and biopsy of the lung showed moderately differentiated adenocarcinoma with epidermal rowth factor receptor exon 21 mutation.
Metachronous triple primary neoplasms with primary prostate cancer, lung cancer and colon cancer.
The patient underwent surgical resection of the right upper lobe of the lung, postoperative stage was T1bN0M0 (stage IA). After 8 cycles of chemotherapy with modified FOLFOX6 regimen (oxaliplatin 85 mg/m, leucovorin 400 mg/m, 5-fluorouracil 400 mg/m on day 1, followed by 5-fluorouracil 2400 mg/m intravenous infusion over 46 hours every 2 weeks), the patient underwent radical resection of colon cancer, and he finished the remaining 4 cycles of modified FOLFOX6 regimen chemotherapy in November 2017.
The patient takes examination every three months, and the results show no recurrence.
When considering MPNs, thorough surveillance by new screening methods is required to detect a second or even third neoplasm at an early stage.
多原发性肿瘤(MPN)较为罕见。大多数MPN为双原发性肿瘤,三原发性肿瘤极为罕见。在此,我们描述一例66岁男性患者,诊断为异时性三原发性肿瘤,分别为原发性前列腺癌、肺癌和结肠癌。
患者于2015年1月出现排尿困难,接受了经尿道前列腺切除术。病理结果显示为前列腺腺泡腺癌,Gleason评分3+3。2017年1月,患者出现下腹部疼痛,随后进行肠镜检查,发现乙状结肠有肿物,正电子发射断层扫描/计算机断层扫描检查显示乙状结肠和右肺上叶有肿物。结肠活检显示为中度分化腺癌,伴有 Kirsten 大鼠肉瘤病毒癌基因同源物外显子2突变,肺部活检显示为中度分化腺癌,伴有表皮生长因子受体外显子21突变。
异时性三原发性肿瘤,分别为原发性前列腺癌、肺癌和结肠癌。
患者接受了右肺上叶手术切除,术后分期为T1bN0M0(IA期)。采用改良FOLFOX6方案(奥沙利铂85mg/m²、亚叶酸钙400mg/m²、第1天5-氟尿嘧啶400mg/m²,随后每2周5-氟尿嘧啶2400mg/m²静脉输注46小时)进行8周期化疗后,患者接受了结肠癌根治术,并于2017年11月完成了剩余4周期的改良FOLFOX6方案化疗。
患者每三个月进行检查,结果显示无复发。
在考虑MPN时,需要采用新的筛查方法进行全面监测,以便早期发现第二个甚至第三个肿瘤。