Posterior mediastinal ganglioneuroblastoma in an adolescent: A case report and review.
Nodoka SekiguchiTakuro NoguchiToshirou FukushimaTakashi KobayashiTakesumi OzawaYoshinori SatoTetsu TakedaKazuo YoshidaTomonobu KoizumiPublished in: Thoracic cancer (2019)
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.
Keyphrases
- young adults
- lymph node
- mental health
- ultrasound guided
- minimally invasive
- end stage renal disease
- ejection fraction
- newly diagnosed
- chronic kidney disease
- prognostic factors
- coronary artery bypass
- bone mineral density
- single cell
- body composition
- patient reported outcomes
- atrial fibrillation
- soft tissue
- acute coronary syndrome