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1.
Pediatr Blood Cancer ; 61(8): 1479-80, 2014 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-24443276

RESUMO

Head and neck radiotherapy in children is associated with significant acute and late morbidities. Temporomandibular joint dysfunction and trismus has been widely reported in patients receiving radiotherapy for sarcomas and nasopharyngeal carcinoma; however, erosion of the mandibular condyle is a rare sequela of modern radiotherapy techniques. In this report, we present three cases of erosion of the temporomandibular joint amongst pediatric patients treated with radiotherapy for distinct head, neck and brain malignancies.


Assuntos
Neoplasias Encefálicas/radioterapia , Irradiação Craniana/efeitos adversos , Neoplasias de Cabeça e Pescoço/radioterapia , Côndilo Mandibular , Doenças Mandibulares/etiologia , Lesões por Radiação , Adolescente , Criança , Humanos , Masculino
2.
J Neurooncol ; 109(2): 349-55, 2012 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-22692563

RESUMO

Clinical experience suggests that craniopharyngiomas may temporarily increase in size after radiation therapy (RT). The study goal is to determine the incidence and natural history of this response in a cohort of patients managed at Children's Healthcare of Atlanta (CHOA) or Emory Healthcare (EHC). Between 08/1998 and 06/2009, 41 children and young adults were diagnosed with craniopharyngioma at CHOA and/or EHC. Of these, 21 received external-beam radiation and were included in our analysis. Serial magnetic resonance imaging (MRI) studies were evaluated volumetrically to assess response to RT. Median age at diagnosis was 8.2 years (range 3.2-23.5 years). Median radiation dose was 54.0 Gy using standard fractionation (1.8-2.0 Gy/day). With median follow-up of 41.3 months (range 7.2-121.8 months), actuarial local control and overall survival rates at 5 years were 78.7 % and 100 %, respectively. Of subjects, 52.4 % of subjects (11 of 21) were noted on serial MRI evaluation to have tumor enlargement (mostly cystic component) after radiation before eventual shrinkage without further intervention. For tumors that expanded, the median volume increase was 33.9 % (range 15.6-224.4 %). Median time to maximal tumor/cyst expansion was 1.5 months (range 1.0-5.0 months). Finally, nearly all patients (20 of 21) showed a measurable objective response to therapy by MRI regardless of ultimate disease control. Median time to maximal response post-radiation, as defined by MRI, was 9.5 months (range 3.5-39.9 months). In summary, RT is effective for managing craniopharyngioma. However, despite good ultimate responses, approximately 50 % of the patients show tumor/cyst expansion on MRI over the first few months post-radiation. Caution should be taken not to subject these patients to "salvage surgery" or cyst aspiration during this early time unless there are other overriding surgical indications. Understanding the natural history of this phenomenon could potentially help guide the management of these craniopharyngioma patients.


Assuntos
Craniofaringioma/patologia , Craniofaringioma/radioterapia , Neoplasias Hipofisárias/patologia , Neoplasias Hipofisárias/radioterapia , Radiocirurgia/métodos , Adolescente , Encéfalo/diagnóstico por imagem , Criança , Pré-Escolar , Craniofaringioma/mortalidade , Fracionamento da Dose de Radiação , Feminino , Seguimentos , Humanos , Imageamento por Ressonância Magnética , Masculino , Neoplasias Hipofisárias/mortalidade , Radiografia , Estudos Retrospectivos , Análise de Sobrevida , Adulto Jovem
3.
Int J Radiat Oncol Biol Phys ; 77(1): 106-12, 2010 May 01.
Artigo em Inglês | MEDLINE | ID: mdl-19695790

RESUMO

PURPOSE: To investigate the incidence, risks, severity, and sequelae of posterior fossa syndrome (PFS) in children with medulloblastoma. METHODS AND MATERIALS: Between 1990 and 2007, 63 children with medulloblastoma at Emory University and Children's Healthcare of Atlanta were treated with craniectomy followed by radiation. Fifty-one patients were assigned to a standard-risk group, and 12 patients were assigned to a high-risk group. Five patients had <1.5-cm(2) residual tumor, 4 had >or=1.5-cm(2) residual tumor, and the remainder had no residual tumor. Eleven patients had disseminated disease. Patients received craniospinal irradiation at a typical dose of 23.4 Gy or 36 Gy for standard- or high-risk disease, respectively. The posterior fossa was given a total dose of 54 or 55.8 Gy. Nearly all patients received chemotherapy following cooperative group protocols. RESULTS: Median follow-up was 7 years. PFS developed in 18 patients (29%). On univariate analysis, brainstem invasion, midline tumor location, younger age, and the absence of radiographic residual tumor were found to be predictors of PFS; the last two variables remained significant on multivariate analysis. From 1990 to 2000 and from 2001 to 2007, the proportions of patients with no radiographic residual tumor were 77% and 94%, respectively. During the same eras, the proportions of patients with PFS were 17% and 39%. Only 4 patients had complete recovery at last follow-up. CONCLUSIONS: The incidence of PFS increased in the latter study period and is proportional to more aggressive surgery. Children with midline tumors exhibiting brainstem invasion are at increased risk. With the increased incidence of PFS and the permanent morbidity in many patients, the risks and benefits of complete tumor removal in all patients need to be reexamined.


Assuntos
Neoplasias Cerebelares/radioterapia , Meduloblastoma/radioterapia , Adolescente , Análise de Variância , Ataxia/epidemiologia , Ataxia/etiologia , Neoplasias Cerebelares/tratamento farmacológico , Neoplasias Cerebelares/patologia , Neoplasias Cerebelares/cirurgia , Criança , Pré-Escolar , Terapia Combinada/métodos , Irradiação Craniana , Intervalo Livre de Doença , Disartria/epidemiologia , Disartria/etiologia , Feminino , Seguimentos , Humanos , Incidência , Masculino , Meduloblastoma/tratamento farmacológico , Meduloblastoma/patologia , Meduloblastoma/cirurgia , Hipotonia Muscular/epidemiologia , Hipotonia Muscular/etiologia , Mutismo/epidemiologia , Mutismo/etiologia , Neoplasia Residual , Complicações Pós-Operatórias/epidemiologia , Dosagem Radioterapêutica , Estudos Retrospectivos , Risco , Síndrome , Adulto Jovem
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