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肌炎的恶性肿瘤。

Malignancy in myositis.

机构信息

Department of Internal Medicine, Good Samaritan Hospital, 5601 Loch Raven Boulevard, Baltimore, MD 21239, USA.

出版信息

Curr Rheumatol Rep. 2011 Jun;13(3):208-15. doi: 10.1007/s11926-011-0169-7.

Abstract

Dermatomyositis is associated with an underlying malignancy in about 24% of cases. This association is also true for polymyositis but is less prominent. The malignancy is usually an adenocarcinoma of the ovary, lung, or gastrointestinal tract in Western countries and nasopharyngeal carcinoma in Southeast Asia, Southern China, and Northern Africa. Factors predictive of malignancy in myositis patients include more severe skin and muscle disease and the absence of overlap connective tissue disease features, such as interstitial lung disease. Anti-p155/140 antibodies have a strong predictive value for malignancy in adult patients. Patients with dermatomyositis or polymyositis require an evaluation for occult malignancy at the time of diagnosis and, in some cases, in the event of a subsequent recurrence. This paraneoplastic phenomenon may stem from an immune reaction to antigens expressed in both cancer cells and regenerating fibers in affected muscle.

摘要

皮肌炎与约 24%的病例的潜在恶性肿瘤有关。这种关联也适用于多发性肌炎,但不太明显。在西方国家,恶性肿瘤通常是卵巢、肺或胃肠道的腺癌,而在东南亚、中国南方和北非则是鼻咽癌。肌炎患者发生恶性肿瘤的预测因素包括更严重的皮肤和肌肉疾病,以及缺乏重叠结缔组织病特征,如间质性肺病。抗 p155/140 抗体对成年患者的恶性肿瘤具有很强的预测价值。皮肌炎或多发性肌炎患者在诊断时以及在某些情况下在随后的复发时需要对隐匿性恶性肿瘤进行评估。这种副肿瘤现象可能源于对受影响肌肉中癌细胞和再生纤维表达的抗原的免疫反应。

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