医学
多发性关节炎
肌炎
低丙种球蛋白血症
病理
胸腺癌
结缔组织
重症肌无力
结缔组织病
关节炎
皮肤病科
疾病
胸腺瘤
自身免疫性疾病
免疫学
抗体
作者
Çişem Yıldız,Büşra Topuz Türkcan,Özge Vural,Deniz Gezgin Yıldırım,Mehmet Arda İnan,Aylar Poyraz,Faruk Güçlü Pınarlı,İrfan Taştepe,Ercan Demir,Emine Nur Sunar Yayla,Pelin Esmeray Şenol,Nihal Karaçayır,Sevcan A. Bakkaloğlu
标识
DOI:10.1111/1756-185x.15187
摘要
Abstract Thymic tumors are very rare neoplasms in children and account for less than 1% of mediastinal tumors in pediatric patients. One‐third of the pediatric patients present with symptoms related to the compression of the tumor mass on the surrounding anatomic structures, and paraneoplastic syndromes such as myasthenia gravis, pure red cell aplasia, acquired hypogammaglobulinemia, and connective tissue disorders, which rarely occur in children with thymic tumors. Herein, we report a case of thymic carcinoma mimicking the symptoms of a connective tissue disease with symmetrical polyarthritis accompanying myositis, fever, weight loss, and malaise in a 15‐year‐old male patient. To our knowledge, this is the first case pediatric thymic carcinoma accompany with severe polyarthritis and myopathy, thus we have reviewed the current literature regarding the cases of thymic malignancies coexisting with paraneoplastic syndromes in children.
科研通智能强力驱动
Strongly Powered by AbleSci AI