nav emailalert searchbtn searchbox tablepage yinyongbenwen piczone journalimg journalInfo searchdiv qikanlogo popupnotification paper paperNew
2025, 11, v.38 5-9
以皮肌炎副癌综合征为首发表现的原发性肺癌四例误诊原因分析
基金项目(Foundation): 国家中医药管理局全国名老中医药专家传承工作室建设项目(国中医药人教函[2021]272号)
邮箱(Email): songef@126.com;
DOI:
摘要:

目的 分析以皮肌炎副癌综合征为首发表现的原发性肺癌患者发病原因、临床特点,并通过病例分析总结以皮肌炎副癌综合征为首发表现的原发性肺癌患者误诊原因及防范措施。方法 回顾分析2022年5月至2023年10月以皮肌炎副癌综合征为首发表现的原发性肺癌4例误诊病例资料。结果 4例患者均出现四肢近端肌无力、特征性皮疹而误诊,被误诊为过敏性皮炎2例、脂溢性皮炎及湿疹各1例。4例给予对应治疗后病情并未好转,行胸部CT检查提示肺部占位性病变,进一步行肺组织穿刺病理学检查后确诊为皮肌炎合并原发性肺癌。误诊时间1~2个月。确诊后4例均行化疗,治疗后均病情好转出院,随访1年3例死亡、1例病情尚稳定。结论 皮肌炎副癌综合征须引起临床医生的警惕,在诊疗过程中要全面分析患者临床特点,当出现四肢近端肌无力及皮肌炎典型皮疹、吞咽困难症状,胸部CT检查提示肺部占位性病变,肿瘤标志物升高时,须考虑皮肌炎合并原发性肺癌的可能,尽早行肺组织穿刺活检以及早明确诊断。

Abstract:

Objective To analyze the causes and clinical characteristics of primary lung cancer patients with paraneoplastic syndrome in dermatomyositis as the initial manifestation, and to summarize the causes of misdiagnosis and preventive measures through case analysis of primary lung cancer patients with paraneoplastic syndrome in dermatomyositis. Methods From May 2022 to October 2023, 4 cases of misdiagnosed primary lung cancer with paraneoplastic syndrome in dermatomyositis as the initial manifestation were retrospectively analyzed. Results Four patients were misdiagnosed as allergic dermatitis(n=2), seborrheic dermatitis(n=1) and eczema(n=1) due to proximal limb muscle weakness and characteristic rash. The condition of 4 patients was not improved after corresponding treatment, and chest CT examination showed lung space occupying lesions, and further lung tissue puncture and pathological examination was performed to confirm dermatomyositis complicated with primary lung cancer. The misdiagnosis lasted 1-2 months. After the diagnosis, all the 4 patients received chemotherapy, and their conditions were improved and discharged. After 1 year of follow-up, 3 patients died and 1 patient was still in stable condition. Conclusion Paraneoplastic syndrome in dermatomyositis should be considered by clinicians, and the clinical characteristics of patients should be comprehensively analyzed during diagnosis and treatment. When there is proximal muscle weakness, dermatomyositis typical rash, dysphagia, chest CT scan showing lung space occupying lesions and elevated tumor markers, the possibility of dermatomyositis combined with primary lung cancer should be considered. Lung biopsy should be performed as early as possible for early diagnosis.

参考文献

[1] AUSSY A, BOYER O, CORDEL N. Dermatomyositis and immunemediated necrotizing myopathies:a window on autoimmunity and cancer[J].Front Immunol, 2017,8:992.

[2]李金朋.以副癌综合征为首发症状的肺癌1例[J].医学信息,2015,28(33):392,393.

[3]孙悦,李岱峰,张寅丽,等.不同首发症状皮肌炎的特点分析[J].河南医学研究,2022,31(5):778-782.

[4]李芳,傅徐泉.181例皮肌炎患者合并肿瘤的临床特点分析[J].医药前沿,2020,10(19):39-41.

[5]中华医学会肿瘤学分会,中华医学会杂志社.中华医学会肿瘤学分会肺癌临床诊疗指南(2021版)[J].中华肿瘤杂志,2021,43(6):591-621.

[6]李邦松.以神经副肿瘤综合征为首发症状六例肺癌误诊分析并文献复习[J].实用心脑肺血管病杂志,2011,19(4):635-636.

[7]白晓芳.肺癌副癌综合征1 2例临床分析[J].中原医刊,2004,31(21):12-13.

[8]李保洲,王振敏,李小峰,等.肺癌副癌综合征误诊分析[J].中国误诊学杂志,2001,1(8):1187-1188.

[9] SHAO C, LI S, SUN Y, et al. Clinical characteristics and prognostic analysis of Chinese dermatomyositis patients with malignancies[J].Medicine(Baltimore), 2020,99(34):e21899.

[10] TANIMOTO K, NAKANO K, KANO S, et al. Classification criteria for polymyositis and dermatomyositis[J].J Rheumatol,1995,22(4):668-674.

[11] FANG Y F, WU Y J, KUO C F, et al. Malignancy in dermatomyositis and polymyositis:analysis of 192 patients[J].Clin Rheumatol, 2016,35(8):1977-1984.

[12] LIU Y, XU L, WU H, et al. Characteristics and predictors of malignancy in dermatomyositis:analysis of 239 patients from northern China[J].Oncol Lett, 2018,16(5):5960-5968.

[13] MOGHADAM-KIA S, ODDIS C V, ASCHERMAN D P, et al.Risk factors and cancer screening in myositis[J].Rheum Dis Clin North Am, 2020,46(3):565-576.

[14] WOO J H, KIM Y J, KIM J J, et al. Mortality factors in idiopathic inflammatory myopathy:focusing on malignancy and interstitial lung disease[J].Mod Rheumatol, 2013,23(3):503-508.

[15] GIOVANNUCCI E, HARLAN D M, ARCHER M C, et al.Diabetes and cancer:a consensus report[J].Diabetes Care,2010,33(7):1674-1685.

[16]朱传安,李艳芹.晚期肿瘤患者血小板聚集率与肌酸激酶同工酶的相关性及其对预后的影响[J].中国老年学杂志,2016,36(8):1900-1901.

[17] CHEN P, XIE J, XIAO R, et al. Clinical analysis for 108 cases of dermatomyositis[J].Zhong Nan Da Xue Xue Bao Yi Xue Ban,2019,44(10):1157-1162.

[18] MARANO A L, CLARKE J M, MORSE M A, et al. Subacute cutaneous lupus erythematosus and dermatomyositis associated with anti-programmed cell death 1 therapy[J].Br J Dermatol,2019,181(3):580-583.

[19] CERIBELLI A, ISAILOVIC N, DE SANTIS M, et al. Myositisspecific autoantibodies and their association with malignancy in Italian patients with polymyositis and dermatomyositis[J].Clin Rheumatol, 2017,36(2):469-475.

[20] CHEN H, PENG Q, YANG H, et al. Increased levels of soluble programmed death ligand 1 associate with malignancy in patients with dermatomyositis[J].J Rheumatol, 2018,45(6):835-840.

[21] MCHUGH N J, TANSLEY S L. Autoantibodies in myositis[J].Nat Rev Rheumatol, 2018,14(5):290-302.

[22] YANG H, PENG Q, YIN L, et al. Identification of multiple cancer-associated myositis-specific autoantibodies in idiopathic inflammatory myopathies:a large longitudinal cohort study[J].Arthritis Res Ther, 2017,19(1):259.

[23] OGAWA-MOMOHARA M, MURO Y, MITSUMA T, et al. Strong correlation between cancer progression and anti-transcription intermediary factor 1γ antibodies in dermatomyositis patients[J].Clin Exp Rheumatol, 2018,36(6):990-995.

[24] BEST M, MOLINARI N, CHASSET F, et al. Use of antitranscriptional intermediary factor-1 gamma autoantibody in identifying adult dermatomyositis patients with cancer:a systematic review and meta-analysis[J].Acta Derm Venereol,2019,99(3):256-262.

[25] OLDROYD A, SERGEANT J C, NEW P, et al. The temporal relationship between cancer and adult onset anti-transcriptional intermediary factor 1 antibody-positive dermatomyositis[J].Rheumatology(Oxford), 2019,58(4):650-655.

[26] LU X, PENG Q, WANG G. The role of cancer-associated autoantibodies as biomarkers in paraneoplastic myositis syndrome[J].Curr Opin Rheumatol, 2019,31(6):643-649.

[27] ZHONG L, YU Z, SONG H. Association of anti-nuclear matrix protein 2 antibody with complications in patients with idiopathic inflammatory myopathies:a meta-analysis of 20 cohorts[J].Clin Immunol, 2019,198:11-18.

[28]李芳,傅徐泉.181例皮肌炎患者合并肿瘤的临床特点分析[J].医药前沿,2020,10(19):39-41.

[29]甄莉,李佩珍,仇丽霞,等.皮肌炎合并肿瘤的危险因素的研究[J].现代预防医学,2001,28(2):143-145.

[30]贾超.多发性肌炎/皮肌炎合并间质性肺炎与肿瘤标志物的关系[D].武汉:华中科技大学,2014.

[31]冯定云,周宇麒,刘翠婷,等.皮肌炎合并肺癌7例报告[J].山东医药,2015,55(42):107.

[32]魏晓荣,桑加拉.以副癌综合征为首发表现的肺癌误诊三例[J].临床误诊误治,2009,22(S1):44.

[33] CASSIUS C, LE BUANEC H, BOUAZIZ J D, et al. Biomarkers in adult dermatomyositis:tools to help the diagnosis and predict the clinical outcome[J].J Immunol Res, 2019,2019:9141420.

[34] HOESLY P M, SLUZEVICH J C, JAMBUSARIA-PAHLAJANI A,et al. Association of antinuclear antibody status with clinical features and malignancy risk in adult-onset dermatomyositis[J].J Am Acad Dermatol, 2019,80(5):1364-1370.

基本信息:

DOI:

中图分类号:R734.2

引用信息:

[1]李矜姚,宋恩峰.以皮肌炎副癌综合征为首发表现的原发性肺癌四例误诊原因分析[J].临床误诊误治,2025,38(11):5-9.

基金信息:

国家中医药管理局全国名老中医药专家传承工作室建设项目(国中医药人教函[2021]272号)

检 索 高级检索

引用

GB/T 7714-2015 格式引文
MLA格式引文
APA格式引文