天津医药
天津醫藥
천진의약
TIANJIN MEDICAL JOURNAL
2015年
4期
419-421
,共3页
马春华%姜镕%李金铎%王斌%孙立伟%吕远
馬春華%薑镕%李金鐸%王斌%孫立偉%呂遠
마춘화%강용%리금탁%왕빈%손립위%려원
脑膜%癌,非小细胞肺%肿瘤循环细胞%脑膜转移%非小细胞肺癌%脑脊液%肿瘤标志物免疫荧光染色-染色体荧光原位杂交
腦膜%癌,非小細胞肺%腫瘤循環細胞%腦膜轉移%非小細胞肺癌%腦脊液%腫瘤標誌物免疫熒光染色-染色體熒光原位雜交
뇌막%암,비소세포폐%종류순배세포%뇌막전이%비소세포폐암%뇌척액%종류표지물면역형광염색-염색체형광원위잡교
meninges%carcinoma,non-small-cell lung%neoplasm circulating cells%leptomeningeal metastasis%non-small cell lung cancer%cerebrospinal fluid%tumor marker immunostaining-FISH
目的:通过观察肿瘤标志物免疫荧光染色-染色体荧光原位杂交技术平台(TM-iFISH)富集并计数肺癌脑膜转移患者脑脊液中的恶性肿瘤细胞,探讨一种新的检测脑脊液中恶性肿瘤细胞的方法。方法选取6例经脑脊液细胞学或头增强MRI扫描确诊的肺癌脑膜转移患者,每例患者经腰椎穿刺获取脑脊液20 mL(共10份),其中7.5 mL应用TM-iFISH技术富集并计数脑脊液中的恶性肿瘤细胞,10 mL行脑脊液细胞学检查,2.5 mL行脑脊液生物化学检查。结果10份脑脊液标本均顺利完成上述检测,其中7份标本通过TM-iFISH技术计数示肿瘤细胞数为3~1823个/7.5 mL脑脊液,3份脑脊液细胞学检查发现肿瘤细胞,9份脑脊液生物化学检查结果蛋白量高于正常值。3例患者治疗后应用TM-iFISH技术再次计数脑脊液恶性肿瘤细胞,2例患者计数较治疗前减少。结论 TM-iFISH技术可以富集并计数肺癌脑膜转移患者脑脊液中恶性肿瘤细胞,可能成为肺癌脑膜转移的诊断和疗效评价方法。
目的:通過觀察腫瘤標誌物免疫熒光染色-染色體熒光原位雜交技術平檯(TM-iFISH)富集併計數肺癌腦膜轉移患者腦脊液中的噁性腫瘤細胞,探討一種新的檢測腦脊液中噁性腫瘤細胞的方法。方法選取6例經腦脊液細胞學或頭增彊MRI掃描確診的肺癌腦膜轉移患者,每例患者經腰椎穿刺穫取腦脊液20 mL(共10份),其中7.5 mL應用TM-iFISH技術富集併計數腦脊液中的噁性腫瘤細胞,10 mL行腦脊液細胞學檢查,2.5 mL行腦脊液生物化學檢查。結果10份腦脊液標本均順利完成上述檢測,其中7份標本通過TM-iFISH技術計數示腫瘤細胞數為3~1823箇/7.5 mL腦脊液,3份腦脊液細胞學檢查髮現腫瘤細胞,9份腦脊液生物化學檢查結果蛋白量高于正常值。3例患者治療後應用TM-iFISH技術再次計數腦脊液噁性腫瘤細胞,2例患者計數較治療前減少。結論 TM-iFISH技術可以富集併計數肺癌腦膜轉移患者腦脊液中噁性腫瘤細胞,可能成為肺癌腦膜轉移的診斷和療效評價方法。
목적:통과관찰종류표지물면역형광염색-염색체형광원위잡교기술평태(TM-iFISH)부집병계수폐암뇌막전이환자뇌척액중적악성종류세포,탐토일충신적검측뇌척액중악성종류세포적방법。방법선취6례경뇌척액세포학혹두증강MRI소묘학진적폐암뇌막전이환자,매례환자경요추천자획취뇌척액20 mL(공10빈),기중7.5 mL응용TM-iFISH기술부집병계수뇌척액중적악성종류세포,10 mL행뇌척액세포학검사,2.5 mL행뇌척액생물화학검사。결과10빈뇌척액표본균순리완성상술검측,기중7빈표본통과TM-iFISH기술계수시종류세포수위3~1823개/7.5 mL뇌척액,3빈뇌척액세포학검사발현종류세포,9빈뇌척액생물화학검사결과단백량고우정상치。3례환자치료후응용TM-iFISH기술재차계수뇌척액악성종류세포,2례환자계수교치료전감소。결론 TM-iFISH기술가이부집병계수폐암뇌막전이환자뇌척액중악성종류세포,가능성위폐암뇌막전이적진단화료효평개방법。
Objective To assess the value of tumor marker immunostaining-FISH (TM-iFISH) technology on concen?trating and enumeration of tumor cells in CSF of lung cancer patients with leptomeningeal metastasis(LM). Methods Six cases of non-small cell lung cancer with leptomeningeal metastasis, which were diagnosed by CSF cytology or enhanced MRI scan, were selected. A total of 20 mL of CSF was collected in each case. TM-iFISH technology was employed to concen?trate and quantify circulating tumor cells in 7.5 mL CSF samples in each case while CSF cytology used 10 mL CSF samples in each case;Finally, the rest 2.5 mL CSF in each case was used for biochemistry assay. Results Ten CSF samples from 6 patients with non-small lung cancer with LM were assayed and tumor cells numbers ranging between 3 and 1 823 every 7.5 mL were found in 7 samples. On the other hand, CSF cytology examination only revealed tumor cells in 3 cases. Using CSF biochemical assay, higher than normal of protein level was found in 9 cases. TM-iFISH technology was employed again in 3 cases of patients who received treatment. Tumor cell count in CSF reduced in 2 out of the 3 cases. Conclusion TM-iFISH technology is a new method for detection and enumeration of tumor cells in the CSF in non-small cell lung cancer patients with leptomeningeal metastasis. This technology present diagnosis and curative values in lung cancer patients with leptomen?ingeal metastasis.