Literature DB >> 9298275

Prognosis of medulloblastoma in infants.

C Di Rocco1, A Iannelli, F Papacci, G Tamburrini.   

Abstract

The prognosis of medulloblastoma in children less than 3 years old is usually considered to be rather poor. However, recent experiences with this type of tumour seem to indicate that survival in this specific subgroup of patients can be longer than expected. Nineteen infants with posterior fossa tumours treated by the authors in the period 1983-1994, all of them with symptoms presenting during the 1st year of life and all operated on before the end of the 2nd year of life, have been retrospectively analysed. Total tumour removal was achieved in 14 cases, subtotal in 1 and partial in 3. One subject underwent only a biopsy of the tumour. In 14 patients a CSF shunt was inserted. Chemotherapy was administered to 18 out of the 19 patients in the series. At the time of the study, 11 children had died (57.9%) and 8 were alive (42.1%; mean survival 86.5 months). One patient died of complications secondary to the surgical treatment. Three patients died because of local recurrence of the tumour after apparent total excision, death supervening 5, 12 and 18 months after the surgical treatment. A further 2 patients in whom total tumour removal had been performed died 3 and 17 months after surgery of local recurrence of the disease associated with regional metastases. Progression of the residual tumour, accompanied by metastatic dissemination in 3 cases, accounted for death in the other 5 patients who did not survive. Brain stem infiltration appeared to be the most significant adverse prognostic factor. All 8 long-term survivors had their tumour totally excised. Five of them underwent radiotherapy when at least 2 years old. On the basis of the results, the authors conclude that the current prognosis of infants with medullo-blastoma is not necessarily any worse than that of older children with the same disease and that chemotherapy can be particularly useful in this subgroup of patients, as shown by 3 long-term survivals obtained in children treated with this type of therapy only.

Entities:  

Mesh:

Substances:

Year:  1997        PMID: 9298275     DOI: 10.1007/s003810050106

Source DB:  PubMed          Journal:  Childs Nerv Syst        ISSN: 0256-7040            Impact factor:   1.475


  6 in total

1.  Endoscopic biopsy interpretation difficulties in a congenital diffuse intracranial teratoma.

Authors:  Federico Di Rocco; Yuichiro Nonaka; Hideo Hamada; Masami Yoshino; Hiromichi Nakazaki; Shizuo Oi
Journal:  Childs Nerv Syst       Date:  2005-03-23       Impact factor: 1.475

2.  Shunt-related abdominal metastases in an infant with medulloblastoma: long-term remission by systemic chemotherapy and surgery.

Authors:  A Fiorillo; G Maggi; A Martone; R Migliorati; R D'Amore; E Alfieri; N Greco; S Cirillo; I Marano
Journal:  J Neurooncol       Date:  2001-05       Impact factor: 4.130

3.  Cytogenetic and histopathologic studies of congenital supratentorial primitive neuroectodermal tumors: a case report.

Authors:  H J Girschick; R Klein; W G Scheurlen; J Kühl
Journal:  Pathol Oncol Res       Date:  2001       Impact factor: 3.201

4.  The invasiveness of five medulloblastoma cell lines in collagen gels.

Authors:  Adrianna Ranger; Warren McDonald; Emi Moore; Rolando Delmaestro
Journal:  J Neurooncol       Date:  2009-07-15       Impact factor: 4.130

5.  Medulloblastoma in childhood-King Edward Memorial hospital surgical experience and review: Comparative analysis of the case series of 365 patients.

Authors:  Dattatraya Muzumdar; Amit Deshpande; Ratnesh Kumar; Ankur Sharma; Naina Goel; Nitin Dange; Abhida Shah; Atul Goel
Journal:  J Pediatr Neurosci       Date:  2011-10

6.  Impact of radiation avoidance on survival and neurocognitive outcome in infant medulloblastoma.

Authors:  L Lafay-Cousin; E Bouffet; C Hawkins; A Amid; A Huang; D J Mabbott
Journal:  Curr Oncol       Date:  2009-12       Impact factor: 3.677

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.