...
首页> 外文期刊>Annals of laboratory medicine. >A Case of Anti-reticulin Antibody-positivity in Metachronous Double Primary Cancer
【24h】

A Case of Anti-reticulin Antibody-positivity in Metachronous Double Primary Cancer

机译:一例异性双原发癌中抗网状蛋白抗体阳性的病例

获取原文
   

获取外文期刊封面封底 >>

       

摘要

Dear Editor, Several studies have demonstrated the relationship between autoantibodies and tumors [ 1 ]. The anti-reticulin antibody (ARA)was first identified in 1971 and was used as a specific marker for gluten-sensitive enteropathy [ 2 , 3 ], playing a supportive role in the diagnosis of celiac disease. However, anti-tissue transglutaminase antibody detection has replaced the ARA method as the single test to diagnose celiac disease. To date, ARA has only been identified in patients with autoimmune enteropathy and other types of autoimmune diseases. However, we observed its presence in a patient who was diagnosed as having metachronous double primary cancer. We evaluated the relationship between ARA and malignancy. A 77-year-old man achieved complete recovery of papillary urothelial carcinoma of the bladder after undergoing transurethral resection of the bladder tumor in October 2003 at Hanyang University Medical Center, Seoul, Korea. In June 2013, he was diagnosed as having adenocarcinoma as a second primary cancer with involvement of multiple lymph nodes and bone metastases. The patient was maintained with hormone therapy and conservative treatment. In October 2014, biochemistry test results showed an alkaline phosphatase level of 176 U/L and AST/ALT levels of 149/166 U/L, both of which were higher than normal levels. The results of viral hepatitis test and complete blood cell count were normal. To differentially diagnose toxic hepatitis, hormone therapy was discontinued. An antinuclear antibody (ANA) test performed to differentially diagnose autoimmune hepatitis was negative. The test tissue was negative for anti-smooth muscle antibody (ASMA) but was positive for R1-ARA ( Fig. 1 ). At that time, the patient had elevated AST/ALT levels due to non-alcoholic fatty liver disease, for which he was solely treated with analgesics. In this case, the second primary cancer developed nine years and eight months after the primary cancer. Although this is a relatively long period, detection of the autoantibody in a patient with double primary cancer may be of general significance. ARA is generally detected by indirect immunofluorescence using three types of rat tissues (stomach, kidney, and liver), and its immunofluorescent patterns are classified into five types (R1, R2, RKC, RAC, and Rs) [ 4 ]. Among these, R1-ARA is specific to untreated celiac disease [ 5 , 6 ]. The R1 pattern is immunopositive in the perivascular area of the stomach, kidney, and liver; the area between the gastric glands; the periglomerular and peritubular areas of the kidney; and the areas surrounding the liver parenchyma, sinusoid, and portal vein of the liver. Natural autoantibodies regulate the immune system. Therefore, it is possible that various types of autoantibodies may be detected in conditions, in which homeostasis is disrupted, in cluding malignant tumors [ 1 ]. In addition, autoantibodies have been transiently detected in patients undergoing treatments such as interleukin therapy for malignant tumors [ 7 , 8 ]. However, to our knowledge, there has been no previously reported case of a patient with autoantibody-positive metachronous double primary cancer. In the current case, R1-ARA was confirmed in a patient with metachronous double primary cancer without a history of bowel disease. This suggests that other mechanisms may be involved in the synthesis of R1-ARA. The current patient did not receive interleukin treatment. However, it is probable that this patient had transient autoantibodies that were only observed during cancer treatment. Alternatively, it is possible that the metachronous double primary cancer occurred as a result of cancer evolution due to genetic defects in the host's immune system. We also consider the possibility that the autoantibodies may have arisen from a systemic inflammatory response. Further studies are warranted to clarify the relationship between the immunofluorescent patterns of ARA and malignant diseases, which will provide more information on the relevant mechanisms. Extensive investigations based on Korean and overseas ARA-positive cases may be helpful for diagnosing and treating patients.
机译:尊敬的编辑,数项研究证明了自身抗体与肿瘤之间的关系[1]。抗网状蛋白抗体(ARA)于1971年首次被鉴定,被用作面筋敏感肠病的特异性标记物[2,3],在乳糜泻的诊断中起辅助作用。但是,抗组织转谷氨酰胺酶抗体检测已取代ARA方法,成为诊断乳糜泻的单一检测方法。迄今为止,仅在患有自身免疫性肠病和其他类型的自身免疫性疾病的患者中鉴定出ARA。但是,我们在诊断为异时双原发癌的患者中观察到了它的存在。我们评估了ARA与恶性肿瘤之间的关系。一名77岁的男子于2003年10月在韩国汉城汉阳大学医学中心接受了经尿道膀胱肿瘤切除术,从而完全治愈了膀胱乳头状尿路上皮癌。 2013年6月,他被诊断为第二大原发性腺癌,涉及多个淋巴结和骨转移。患者接受激素治疗和保守治疗。 2014年10月,生化测试结果显示碱性磷酸酶水平为176 U / L,AST / ALT水平为149/166 U / L,均高于正常水平。病毒性肝炎测试和全血细胞计数结果正常。为了鉴别诊断中毒性肝炎,已停止激素治疗。为鉴别诊断自身免疫性肝炎而进行的抗核抗体(ANA)测试为阴性。测试组织的抗平滑肌抗体(ASMA)阴性,但R1-ARA阳性(图1)。当时,由于非酒精性脂肪肝疾病,患者仅接受止痛药治疗,AST / ALT水平升高。在这种情况下,第二原发癌在原发癌后九年零八个月发展。尽管这是一个相对较长的时期,但在患有双重原发癌的患者中检测自身抗体可能具有普遍意义。通常使用三种类型的大鼠组织(胃,肾脏和肝脏)通过间接免疫荧光检测ARA,并将其免疫荧光模式分为五种类型(R1,R2,RKC,RAC和Rs)[4]。其中,R1-ARA特异于未经治疗的乳糜泻[5,6]。 R1型在胃,肾和肝的血管周围区域呈免疫阳性;胃腺之间的区域;肾脏的肾小球周围和肾小管周围区域;以及肝实质,肝窦和肝门静脉周围的区域。天然自身抗体调节免疫系统。因此,有可能在包括体内恶性肿瘤在内的体内稳态被破坏的条件下检测到各种类型的自身抗体[1]。此外,已经在接受诸如白细胞介素治疗恶性肿瘤等治疗的患者中短暂检测到自身抗体[7,8]。然而,据我们所知,以前没有报道自身抗体阳性的异时双原发癌患者。在当前情况下,R1-ARA已在无肠病史的异时双原发癌患者中得到确认。这表明R1-ARA的合成可能涉及其他机制。当前患者未接受白介素治疗。但是,该患者可能具有仅在癌症治疗期间观察到的短暂性自身抗体。或者,由于宿主免疫系统的遗传缺陷,癌症发展可能导致异时双原发癌的发生。我们还考虑了自身抗体可能来自全身性炎症反应的可能性。有必要进行进一步的研究来阐明ARA的免疫荧光模式与恶性疾病之间的关系,这将提供有关相关机制的更多信息。基于韩国和国外ARA阳性病例的广泛调查可能有助于诊断和治疗患者。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号