We report an exceptional case of a very late local failure in a 9-year-old boy presenting with a chordoma of the cranio-cervical junction. The child was initially treated with a combination of surgical resection followed by high dose photon–proton radiation therapy. This aggressive therapy allowed a 9-year remission with minimal side-effects. Unfortunately, he subsequently presented with a local failure managed with a second full-dose course of protons. The child died one year later from local bleeding of unclear etiology
Rates and characteristics of intracerebral cavernous malformations after cranial radiation therapy r...
Brain tumors represent the most frequent solid malignancy in children and the first cause of cancer-...
Paediatric chordomas are rare malignant tumours arising from primitive notochordal remnants with a h...
We report an exceptional case of a very late local failure in a 9-year-old boy presenting with a cho...
Background: : Radiogenic malignancies require cure of the primary disease and a prolonged survival. ...
BACKGROUND: Chordomas are rare, slow-growing malignant neoplasms derived from remnants of the emb...
INTRODUCTION: The majority of chordomas occur between the fifth and seventh decades of life and are ...
Introduction: Papillary tumors of the pineal region (PTPR) are rare brain tumors characterized by fr...
Contains fulltext : 167899.pdf (Publisher’s version ) (Open Access)CASE REPORT: Th...
Introduction: Burkitt lymphoma (BL) is rare, but an aggressive malignancy. Central nervous system Bu...
PURPOSE: In this study factors are analyzed that may potentially influence the site of failure in pe...
We hereby report a case of a 10-year-old girl in whom neurosurgery was performed for cerebellar verm...
Lymphoepithelioma rarely develops in children. In its early stage it may manifest itself only as enl...
BACKGROUND: Papillary tumor of the pineal region (PTPR) is a rare grade II-III pineal lesion with pe...
Childhood-onset craniopharyngiomas are partly cystic embryonic malformations of the sellar/parasella...
Rates and characteristics of intracerebral cavernous malformations after cranial radiation therapy r...
Brain tumors represent the most frequent solid malignancy in children and the first cause of cancer-...
Paediatric chordomas are rare malignant tumours arising from primitive notochordal remnants with a h...
We report an exceptional case of a very late local failure in a 9-year-old boy presenting with a cho...
Background: : Radiogenic malignancies require cure of the primary disease and a prolonged survival. ...
BACKGROUND: Chordomas are rare, slow-growing malignant neoplasms derived from remnants of the emb...
INTRODUCTION: The majority of chordomas occur between the fifth and seventh decades of life and are ...
Introduction: Papillary tumors of the pineal region (PTPR) are rare brain tumors characterized by fr...
Contains fulltext : 167899.pdf (Publisher’s version ) (Open Access)CASE REPORT: Th...
Introduction: Burkitt lymphoma (BL) is rare, but an aggressive malignancy. Central nervous system Bu...
PURPOSE: In this study factors are analyzed that may potentially influence the site of failure in pe...
We hereby report a case of a 10-year-old girl in whom neurosurgery was performed for cerebellar verm...
Lymphoepithelioma rarely develops in children. In its early stage it may manifest itself only as enl...
BACKGROUND: Papillary tumor of the pineal region (PTPR) is a rare grade II-III pineal lesion with pe...
Childhood-onset craniopharyngiomas are partly cystic embryonic malformations of the sellar/parasella...
Rates and characteristics of intracerebral cavernous malformations after cranial radiation therapy r...
Brain tumors represent the most frequent solid malignancy in children and the first cause of cancer-...
Paediatric chordomas are rare malignant tumours arising from primitive notochordal remnants with a h...