3rd Dept of Internal Medicine, Division of Immunology, University of Debrecen Medical and Health Science Center, Debrecen, Hungary.
Joint Bone Spine. 2011 Mar;78(2):209-11. doi: 10.1016/j.jbspin.2010.08.018. Epub 2010 Nov 19.
We present a female with anti-Jo-1 positive polymyositis and lung adenocarcinoma. Her polymyositis diagnosis was based on her clinical symptoms, electromyography results, and highly elevated muscle enzymes, including creatine kinase and lactate-dehydrogenase. Anti-Jo-1 positivity, leukocytosis and elevated tumor markers: CA 15-3 and CA 72-4 were also certified at the diagnosis. Her malignancy was finally diagnosed by transthoracic needle biopsy, two years after the appearance of first symptoms of polymyositis. After surgical removal of the tumor, polymyositis was in remission. Due to the symptoms mentioned above and the coincidence of the tumor, a paraneoplastic myositis was suspected.
我们报告了一例抗 Jo-1 阳性多发性肌炎合并肺腺癌患者。其多发性肌炎的诊断基于临床症状、肌电图结果和显著升高的肌酶,包括肌酸激酶和乳酸脱氢酶。抗 Jo-1 阳性、白细胞增多和肿瘤标志物升高:CA 15-3 和 CA 72-4 也在诊断时得到证实。两年后,在出现多发性肌炎的最初症状后,通过经胸针吸活检最终诊断为恶性肿瘤。肿瘤切除后,多发性肌炎缓解。由于上述症状和肿瘤的巧合,怀疑为副肿瘤性肌炎。