Thymic carcinoma presenting with overlap polyarthritis and myositis: A rare paraneoplastic syndrome in childhood

Author:

Yıldız Çisem1ORCID,Türkcan Büşra Topuz2,Vural Özge2,Gezgin Yıldırım Deniz1ORCID,İnan Mehmet Arda3,Poyraz Aylar3,Pınarlı Faruk Güçlü2,Taştepe İrfan4,Demir Ercan5,Sunar Yayla Emine Nur1ORCID,Esmeray Şenol Pelin1,Karaçayır Nihal1,Bakkaloğlu Sevcan A.1

Affiliation:

1. Department of Pediatric Rheumatology Gazi University Faculty of Medicine Ankara Turkey

2. Department of Pediatric Oncology Gazi University Faculty of Medicine Ankara Turkey

3. Department of Medical Pathology Gazi University Faculty of Medicine Ankara Turkey

4. Department of Thoracic Surgery Gazi University Faculty of Medicine Ankara Turkey

5. Department of Pediatric Neurology Gazi University Faculty of Medicine Ankara Turkey

Abstract

AbstractThymic 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.

Publisher

Wiley

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