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Neonatal Neoplasms

Publication at Second Faculty of Medicine |
2003

Abstract

In this report authors describe malignant neoplasms diagnosed in newborns <28 days, who were treated in the Department of Pediatric Oncology and Haematology Section of the 2nd Department of Pediatrics, Faculty Hospital Motol between 1990 - 2000. During this period twenty one neonates (9 boys and 12 girls) with neoplasms were diagnosed.

The histologic diagnoses were neuroblastoma (n = 11), germ cell tumor/teratoma (n = 5), retinoblastoma (n = 2), congenital fibrosarcoma (n = 1), alveolar rhabdomyosarcoma (n = 1), acute lymphoblastic leukaemia (n = 1). Diagnosis was established between 1 - 8 days after delivery (median 2 days).

Therapy: eleven patients were treated with surgery alone - neuroblastoma (n = 7), sacrococcygeal teratoma (n = 3), congenital fibrosarcoma (n = 1), six patients with surgery and chemotherapy - neuroblastoma (n = 4), germ cell tumor (n = 2)). Two patients with retinoblastoma were treated with chemotherapy and concomitant local laser therapy.

Radiotherapy treatment was necessary in two patients - disease progression (retinoblastoma) and relapse (neuroblastoma). One patient with a relapse of germ cell tumor underwent megachemotherapy with reinfusion of autologous progenitor stem cells.

Fifteen children (71%) are long-term survivors, two patients succumbed to the disease progression and one patient to the toxic complications related to the treatment. Three patients (15%) are lost to follow up.

Follow up of survivors ranges from 1 day - 134 months (median 67 m.). No associated anomalies were noticed.

Familiar genetic predisposition was established in two patients with retinoblastoma.