目的 报道10例血清CA19-9明显升高的胆管良性疾病病例。
方法 回顾性分析2004年1月至2006年3月期间我院收治并经手术证实的10例血清CA19-9明显升高( gt;500 U/ml)的胆管良性病变病例。
结果 患者中男4例,女6例,年龄30~85岁,CA19-9为532.32~12 000.00 U/ml,除1例患者CA125轻度升高外,其他患者血清CEA、CA125及AFP均正常。胆总管结石8例,肝内胆管结石1例,原发性硬化性胆管炎1例; 除1例外均存在不同程度阻塞性黄疸。经治疗后8例CA19-9水平在30 d内降至正常,另2例分别于术后2个月和3个月内降至正常。
结论 CA19-9在胆管恶性肿瘤诊断方面的意义仍需进一步研究。
Citation:
费健,王建承,陈胜,邓漾,朱坚,张卓,许志伟,陆晔,吴卫泽,雷若庆,韩天权,张圣道. Extraordinarily Elevated CA19-9 Levels in Patients with Benign Disease of Biliary Tract (Report of 10 Cases). CHINESE JOURNAL OF BASES AND CLINICS IN GENERAL SURGERY, 2007, 14(5): 580-582. doi:
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Murray MD, Burton FR, Di Bisceglie AM. Markedly elevated serum CA19-9 levels in association with a benign biliary stricture due to primary sclerosing cholangitis [J]. J Clin Gastroenterol, 2007; 41(1)∶115.
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Ogawa T, Yokoi H, Kawarada Y. A case of inflammatory pseudotumor of the liver causing elevated serum CA19-9 levels [J]. Am J Gastroenterol, 1998; 93(12)∶2551.
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Trompetas V, Panagopoulos E, Ramantanis G. Gall-bladder agenesis presenting with obstructive jaundice and elevated CA19-9 [J]. Acta Chir Belg, 2004; 104(3)∶347.
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Basso D, Meggiato T, Fabris C, et al. Extra-hepatic cholestasis determines a reversible increase of glycoproteic tumour markers in benign and malignant diseases [J]. Eur J Clin Invest, 1992; 22(12)∶800.
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- 1. Minato H, Nakanuma Y, Terada T. Expression of blood group-related antigens in cholangiocarcinoma in relation to non-neoplastic bile ducts [J]. Histopathology, 1996; 28(5)∶411.
- 2. Maestranzi S, Przemioslo R, Mitchell H, et al. The effect of benign and malignant liver disease on the tumour markers CA19-9 and CEA [J]. Ann Clin Biochem, 1998; 35(Pt 1)∶99.
- 3. Paganuzzi M, Onetto M, Marroni P, et al. CA19-9 and CA50 in benign and malignant pancreatic and biliary diseases [J]. Cancer, 1988; 61(10)∶2100.
- 4. 秦兴雷, 李志强, 石景森, 等. 血清和胆汁CA19-9联合检测对诊断胆道良恶性病变的价值 [J]. 中国普外基础与临床杂志, 2000; 7(3)∶161.
- 5. Bjornsson E, Kilander A, Olsson R. CA19-9 and CEA are unreliable markers for cholangiocarcinoma in patients with primary sclerosing cholangitis [J]. Liver, 1999; 19(6)∶501.
- 6. Patel AH, Harnois DM, Klee GG, et al. The utility of CA19-9 in the diagnoses of cholangiocarcinoma in patients without primary sclerosing cholangitis [J]. Am J Gastroenterol, 2000; 95(1)∶204.
- 7. Robertson AG, Davidson BR. Mirizzi syndrome complicating an anomalous biliary tract: a novel cause of a hugely elevated CA19-9 [J]. Eur J Gastroenterol Hepatol, 2007; 19(2)∶167.
- 8. Murray MD, Burton FR, Di Bisceglie AM. Markedly elevated serum CA19-9 levels in association with a benign biliary stricture due to primary sclerosing cholangitis [J]. J Clin Gastroenterol, 2007; 41(1)∶115.
- 9. Katsanos KH, Kitsanou M, Christodoulou DK, et al. High CA19-9 levels in benign biliary tract diseases. Report of four cases and review of the literature [J]. Eur J Intern Med, 2002; 13(2)∶132.
- 10. Albert MB, Steinberg WM, Henry JP. Elevated serum levels of tumor marker CA19-9 in acute cholangitis [J]. Dig Dis Sci, 1988; 33(10)∶1223.
- 11. Lin CL, Changchien CS, Chen YS. Mirizzi’s syndrome with a high CA19-9 level mimicking cholangiocarcinoma [J]. Am J Gastroenterol, 1997; 92(12)∶2309.
- 12. Ogawa T, Yokoi H, Kawarada Y. A case of inflammatory pseudotumor of the liver causing elevated serum CA19-9 levels [J]. Am J Gastroenterol, 1998; 93(12)∶2551.
- 13. Trompetas V, Panagopoulos E, Ramantanis G. Gall-bladder agenesis presenting with obstructive jaundice and elevated CA19-9 [J]. Acta Chir Belg, 2004; 104(3)∶347.
- 14. Basso D, Meggiato T, Fabris C, et al. Extra-hepatic cholestasis determines a reversible increase of glycoproteic tumour markers in benign and malignant diseases [J]. Eur J Clin Invest, 1992; 22(12)∶800.