Thoracic Cancer (Feb 2020)

Posterior mediastinal ganglioneuroblastoma in an adolescent: A case report and review

  • Nodoka Sekiguchi,
  • Takuro Noguchi,
  • Toshirou Fukushima,
  • Takashi Kobayashi,
  • Takesumi Ozawa,
  • Yoshinori Sato,
  • Tetsu Takeda,
  • Kazuo Yoshida,
  • Tomonobu Koizumi

DOI
https://doi.org/10.1111/1759-7714.13277
Journal volume & issue
Vol. 11, no. 2
pp. 451 – 455

Abstract

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Ganglioneuroblastoma is an uncommon malignant tumor of the sympathetic nervous system, which is considered a disease of children with the majority of cases in patients less than four years old and it rarely occurs in adults. We encountered a very unusual case of a posterior mediastinal ganglioneuroblastoma that developed in a 17‐year‐old male adolescent who underwent successful excision of the mediastinal mass and remained stable postoperatively. However, he developed lumbago one year after the surgery. Radiographic findings revealed osteolytic lesions in the lumbar vertebra and histological analysis confirmed bone metastasis of ganglioneuroblastoma. Here, we report the clinical course and present a review of the literature regarding adolescent and adult onset mediastinal ganglioneuroblastoma.

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