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

Int J Rheum Dis. 2024 May;27(5):e15187. doi: 10.1111/1756-185X.15187.

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.

Keywords: arthritis; malignancy; paraneoplastic syndrome; thymic carcinoma.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Adolescent
  • Arthritis* / diagnosis
  • Arthritis* / etiology
  • Biopsy
  • Humans
  • Male
  • Myositis* / complications
  • Myositis* / diagnosis
  • Paraneoplastic Syndromes* / diagnosis
  • Paraneoplastic Syndromes* / etiology
  • Thymectomy
  • Thymoma* / complications
  • Thymoma* / diagnosis
  • Thymus Neoplasms* / complications
  • Thymus Neoplasms* / diagnosis
  • Treatment Outcome