Dai Yuanrong, Li Ping, Yan Sunshun, Xia Xiaodong, Li Zhixiong, Xia Mengling
Department of Respiratory Medicine, The Second Affiliated Hospital, Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, China.
Department of Respiratory Medicine, The People's Hospital of Yichun City, Yichun, China.
Clin Respir J. 2016 Jul;10(4):495-9. doi: 10.1111/crj.12229. Epub 2014 Nov 26.
Paraneoplastic syndrome is a disease or symptom that is the consequence of cancer in the body but, unlike mass effect, is not due to the local presence of cancer cells. An overlap of two paraneoplastic syndromes secondary to lung cancer in a patient is very rare. In order to improve the diagnosis of two paraneoplastic syndromes secondary to lung cancer, we reported an overlap of two paraneoplastic syndromes secondary to lung squamous carcinoma in a patient.
We reported a case of a 60-year-old male smoker who presented multiple erythematous lesions for 6 months with progressive proximal muscular weakness, and developed to dysphonia in 2 months. His chest computed tomography showed a spiculate pulmonary nodule near the hilar in the right upper lobe and mediastinal lymph nodes enlargement. Lung biopsy showed squamous cell carcinoma. The patient's blood test revealed elevated creatine kinase levels. Electromyography results were consistent with moderate myopathy accompanied with a pattern suggestive of Lambert-Eaton myasthenic syndrome.
So we made the diagnosis of an overlap of two paraneoplastic syndromes (dermatomyositis and Lambert-Eaton myasthenic syndrome) secondary to lung squamous carcinoma.
Recognition of paraneoplastic syndrome is crucial for early diagnosis of lung cancer because up to 80% of patients may present paraneoplastic syndromes before any other direct indication of malignancy. Early diagnosis and treatment of paraneoplastic syndrome is also important because delayed diagnosis may result in rapid disease progression and irreversible neurological damage.
副肿瘤综合征是一种疾病或症状,是体内癌症的结果,但与占位效应不同,它并非由癌细胞的局部存在所致。肺癌继发的两种副肿瘤综合征在同一患者中重叠的情况非常罕见。为了提高对肺癌继发的两种副肿瘤综合征的诊断,我们报告了一例肺鳞状细胞癌继发的两种副肿瘤综合征重叠的病例。
我们报告了一例60岁男性吸烟者,他出现多处红斑性病变6个月,伴有进行性近端肌无力,并在2个月内发展为声音嘶哑。他的胸部计算机断层扫描显示右上叶肺门附近有一个毛刺状肺结节以及纵隔淋巴结肿大。肺活检显示为鳞状细胞癌。患者的血液检查显示肌酸激酶水平升高。肌电图结果与中度肌病一致,并伴有提示兰伯特-伊顿肌无力综合征的模式。
因此我们诊断该患者为肺鳞状细胞癌继发的两种副肿瘤综合征(皮肌炎和兰伯特-伊顿肌无力综合征)重叠。
认识副肿瘤综合征对于肺癌的早期诊断至关重要,因为高达80%的患者可能在出现任何其他恶性肿瘤的直接迹象之前就出现副肿瘤综合征。副肿瘤综合征的早期诊断和治疗也很重要,因为延迟诊断可能导致疾病快速进展和不可逆的神经损伤。